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Posted by Linda, 17:35 21 November 2006I'll try to include all the info I've posted in various places on the forum, here. I haven't checked the links in a while so apologies if any of them don't work.
Books and links: www.breggin.com/Fromprozac.pbreggin.2001.pdf www.breggin.com/brain-disablingch1.html www.breggin.com/braindisabling.pdf www.breggin.com/courtfiling.pbreggin.2006.pdf www.antidepressantsfacts.com/scientists.htm (Probably some of the most accurate info available today) www.thomasjmoore.com/pages/depress.shtml (the truth about the drug industry) www.chaada.org/plog/index.php?op=ViewArticle&articleId=212&blogId=1 www.chaada.org/plog/index.php?op=ViewArticle&articleId=216&blogId=1 www.medicine.plosjournals.org/perlserv/?request=get-document&doi=10.1371/journal.pmed.0020392 www.medicine.plosjournals.org/perlserv/?request=get-document&doi=10.1371/journal.pmed.0020124 www.medicine.plosjournals.org/perlserv/?request=get-document&doi=10.1371/journal.pmed.0030185 www.medicine.plosjournals.org/perlserv/?request=get-document&doi=10.1371/journal.pmed.0020138 www.observer.co.uk/magazine/story/0,11913,706297,00.html (Part 1 -- The Chemistry of Happiness) www.observer.co.uk/magazine/story/0,11913,706299,00.html (Part 2 -- The Chemistry of Happiness) www.network54.com/Forum/281849/message/1148149237/Looking+back+over+Fifty+years+of+psychopharmacology+..Heather+Ashton%2C+Emeritus+Professor (A revealing lecture about the recent history of psychopharmacology by a retired doctor) www.network54.com/Forum/182310/ www.network54.com/Forum/281849/ -- Prozac Backlash : Overcoming the Dangers of Prozac, Zoloft, Paxil, and Other Antidepressants with Safe, Effective Alternatives - by Joseph Glenmullen, M.D. -- Prozac and the New Antidepressants : What You Need to Know About Prozac, Zoloft, Paxil, Luvox, Wellbutrin, Effexor, Serzone, Vestra, Celexa, St. John's Wort - by William S. Appleton -- Prozac: Panacea or Pandora?- by Ann Blake Tracy, Ph.D. A treasure trove of information you will not find elsewhere. Ann is a pioneer in revealing the true nature of antidepressant drugs. -- The Antidepressant Era - by David Healy, M.D. -- Molecules of Emotion - by Candace Pert, Ph.D. -- Psychiatric Survivor- from misdiagnosed patient on a mental ward to hospital director. The Autobiography of A. Mark Bedillion, MS.Ed.,C.A.C. -- The Noonday Demon - Andrew Solomon -- The Shooting Drugs - Prozac and its Generation Exposed on the Internet - by Donna Smart -- Challenging the Therapeutic State : Critical Perspectives on Psychiatry and the Mental Health System - by David Cohen -- The Manufacture of Madness : A Comparative Study of the Inquisition and the Mental Health Movement - by Thomas S. Szasz -- Mad in America: Bad Science, Bad Medicine, and the Enduring Mistreatment of the Mentally Ill - by Bob Whitaker -- Prescription for Disaster -The Hidden Dangers in Your Medicine Cabinet - by Thomas J. Moore -- The Power to Harm Mind, Medicine and Murder on Trial: The Westbecker Prozac Case - by John Cornwell -- Psychiatric Drugs Explained (second edition) by David Healy, M.D. -- Toxic Psychiatry by Peter Breggin -- The Antidepressant Fact Book by Peter Breggin -- Brain-disabling Treatments in Psychiatry by Peter Breggin -- Mad In America: Bad Science, Bad Medicine, and The Enduring Mistreatment of the Mentally Ill by Robert Whitaker -- Warning: Psychiatry Can Be Hazardous to Your Mental Health by William Glasser --Blaming the Brain: The Truth About Drugs and Mental Health by Elliot Valenstein -- Psychiatric Drugs Shorten Life Span http://www.stopshrinks.org/reading_room/antipsych/psych_drugs_shorten _life.html -- Against Depression, a Sugar Pill Is Hard to Beat http://www.stopshrinks.org/articles/sugar.htm -- Why Psychiatric Drugs Are Always Bad by Douglas C. Smith, M.D. -- A list of books http://www.outlookcities.com/psych/ -- http://www.antidepressantsfacts.com/articles.htm -- THE DARK SIDE OF PSYCHIATRY http://www.oikos.org/antipsicen.htm -- THE CRITICAL PSYCHIATRY WEBSITE http://www.critpsynet.freeuk.com/antipsychiatry.htm -- PROZAC SURVIVORS http://www2.netdoor.com/~bill/prosurv/prosurv.html -- ANTIDEPRESSANTS FACTS www.antidepressantsfacts.com -- INTERNATIONAL COALITION FOR DRUG AWARENESS http://www.drugawareness.org/ -- HEALTHY SKEPTICISM http://www.healthyskepticism.org/ ALLIANCE FOR HUMAN RESEARCH PROTECTION www.ahrp.org | |
Posted by Linda, 17:38 21 November 2006Some info and wisdom from my Withdrawal and Recovery group.
BENEFITS OF DISCONTINUING SSRIs: 1. Every day you are taking one of these drugs, more damage is being done to your brain and body. There is no escaping this. Psychotropic drugs alter brain chemistry and brain structure in ways nature never would. 2. They are ALL damaging to the heart and those that manipulate serotonin in particular, are damaging to your entire circulatory system. 3. All of these drugs, perhaps with the exception of the benzodiazepines, damage your entire hormonal system. Most people think of hormones as bweing only estrogen and testosterone. That is not correct. There are many hormones in the body including serotonin and insulin. Antidepressants and antipsychotics alter how your body metabolizes insulin which damages many other body processes including certain organs. 5. All psychotropic drugs damage your nervous system. Your nervous system is the centeral network in your body involved in all bodily processes. 4. Scores of articles, websites, and books detail the dangers of psychotropic drugs. The basic fact is that your life is shortened and you will face illnesses, chronic ones, as a result of continuing these drugs. ******** Very few people escape the ravages of these drugs; however, in many cases, people do not connect what they are experiencing with the drugs they took. Some no longer can lose weight as they used to. This is because the drugs disrupt proper insulin metabolism. How? Serotonin and insulin are intimately connected. When you alter serotonin, you alter insulin. ADs are harmful to the cardiovascular system. Excess serotonin damages arteries. All SSRIs cause excess serotonin -- at least initially. SSRIs leave you with fewer serotonin receptors than you had prior to taking the drug. All ADs do this to the receptors of whatever neurotransmitters they affect. People end up more tired than ever. Eventually, some get fibromyalgia or chronic fatigue syndrome. They don't associate it with the drugs. All hormones are adversely affected. People feel less emotionally. They are less empathic with others. Psychotropic drugs turn people into carbohydrate addicts. These are just a few of the things that psychotropic drugs do. As for how this can be allowed to continue -- the bottom line is, follow the money. This is a multi-billion-dollar industry that is growing every day. Only the best industrial psychologists and Madison Avenue advertising firms work for the pharmaceutical industry. Also, consider the role the drug industry plays in the stock market. What would happen if they were really called to task and made to stop selling drugs that don't work or cause harm? Most likely, the entire economic underpinning of the US would collapse. Final note -- it is not just psychotropic drugs that are dangerous and lacking in efficacy being foisted upon the public. | |
Posted by Linda, 18:17 21 November 2006One more piece of info to add here: an excerpt from "How to Lift Depression . . . Fast (The Human Givens Approach)". The section in it about antidepressants is short, but very telling I feel. This book does not advocate their use.
Why Claims for SSRIs May Be Overrated Ironically, psychiatrists were highly delighted by the SSRIs, when they came on the scene in the 1980s, because they appeared to cause fewer side effects than tricyclics, the antidepressants in use at that time. The enthusiasm has been happily promoted by the drug companies, as the SSRIs are considerably more expensive. However, many researchers now question whether these drugs ever really did much of what they were supposed to do at all. SSRIs are designed to affect levels of serotonin in the brain but only five percent of serotonin is found in the brain; the rest is distributed throughout the body, to do things such as help regulate the digestive system, the pumping of blood around the body and the workings of the reproductive system. So the drugs affect a lot else besides serotonin levels in the brain. It could even be, according to some critics, that SSRIs don't really have an antidepressant effect at all but merely a general calming down effect. We can see that there are clear grounds for this concern if we look at the way SSRIs ended up on the market. When new drugs are developed, they have to be tested in rigorously controlled clinical trials, in which usually the efficacy of the new drug is compared with that of a placebo (a dummy drug). This means ensuring that neither the doctors prescribing the drugs nor the patients taking them know who is receiving which (a procedure called blinding). This is important because, if either doctors or patients know which is being taken, then the placebo effect may occur. This is when our own expectation of getting better (through the new drug) has the effect of stimulating our internal healing powers, rather than, or as well as, recovery due to the drug. (Conversely, disappointment at realising we are on a dummy pill is likely to reduce our expectation of getting better, and thus damp down any natural healing power.) But, just as there are legal loopholes for avoiding the due amount of tax, so there are legal ways of manipulating the placebo effect to make a drug look more effective than it really is. For instance, in trials using a placebo drug and an active drug, experimenters carrying out the trial on behalf of the drug company may use placebo washout procedures. This means that everyone is given the placebo first and all those who get significantly better are taken out of the trial at that point. Then the people who are left are given either the placebo or the real drug. The effect, of course, is that the experimenters already know that those on the placebo aren't so likely to do very well, as they are the ones whose symptoms didn't get better the first time they had a placebo. So, when their wellness is compared with that of people who took the real drug, it will make the drug look a lot more effective than perhaps it really is. To give an example, 100 people enter the trial and all are given a placebo. Of these, 20 get better and are removed from the trial. The remaining 80 are divided into two groups, half receiving the placebo and half the drug. Five of those on the placebo get better and 30 of those on the drug. It looks as if the drug is six times better than the placebo. In fact, counting in all the people who started the trial, it is not much better than the placebo at all -- 25 getting better on the placebo and 30 on the drug. It might even be the case that many people in trials do realise when they are taking an active drug (perhaps they experience particular side effects) and so their expectation of getting better may be partly responsible anyway. Recently some researchers looked at 191 double-blind placebo-controlled trials (selected at random from trials published in five leading general medical journals and in psychiatry journals), and found that researchers in just 15 of the trials made checks on whether blinding had worked. In just five trials was blinding claimed to be successful and for only two of those five trials was any evidence presented to justify the claim of success! The likelihood that antidepressant effectiveness may be overrated is strengthened by another important piece of evidence. Trials that do not find a new drug significantly more effective than placebo usually go unpublished. When researchers took advantage of the American freedom of information laws to look at both published and unpublished trials, they found that the overall reduction in symptoms in more than 20,000 people who took part in trials was 40 per cent for antidepressants and 30 per cent for placebo. A survey of 50 trials showed that 54 per cent of people benefitted from antidepressants but 46 percent did not. Just recently, researchers in Iceland collected nationwide data on the prescribing of antidepressant drugs and on people's recovery from mental illness. They found that sales of antidepressants went up by over 16 per cent a year after SSRIs were introduced to Iceland but that there was no noticeable impact on psychiatric health at all. *********** It has now come to light that taking antidepressants can even have serious long-term health consequences. SSRIs raise serotonin availability in the body. Serotonin is the brain chemical that has the effect of lifting mood. However, it is now so widely recognised that drugs in this group can cause a worsening of symptoms and the development of violent or suicidal thoughts that the FDA in America wants clear warnings put on their labels. Respected Harvard psychiatrist Dr. Joseph Glenmullen trawled through a mountain of psychiatric journals and found evidence of thousands of cases of neurological side effects occurring with SSRIs. These included tics such as eye and lip twitching, agitation, severe restlessness, muscle spasms ranging from mild to severe (body parts becoming locked) and Parkinsonism. He points out that all of these side effects were also caused in people prescribed major tranquillisers -- drugs which, decades ago, used to be prescribed even to children for symptoms such as mild anxiety, insomnia and hyperactivity. Indeed, in 2004, safety worries led the UK government's Committee on Safety of Medicines to recommend that some SSRIs are not given to children under the age of 18 and others are still under review. Because withdrawal effects of SSRIs may include symptoms similar to the symptoms of depression, such as fatigue and apathy, doctors often assume, when patients complain of them, that the depression hasn't lifted yet and prescribe the drug for longer. Be aware if this might be the case for you. | |
Posted by BWAD Squirrel, 20:41 21 November 2006American Journal of Psychiatry:
Roy H. Perlis, Clifford S. Perlis, Yelena Wu, Cindy Hwang, Megan Joseph, and Andrew A. Nierenberg (2005) Industry Sponsorship and Financial Conflict of Interest in the Reporting of Clinical Trials in Psychiatry. Am J Psychiatry, 162: 1957 - 1960. British Journal of Psychiatry: Moncrieff, J. (2002) The antidepressant debate. British Journal of Psychiatry, 180(3): 193-194. Andrews, G. (2001) Placebo response in depression: bane of research, boon to therapy. British Journal of Psychiatry, 178, 192-194. Even, C., Siobud-Dorocant, E. & Dardennes, R. M. (2000) Critical approach to antidepressant trials. Blindness protection is necessary, feasible and measurable. British Journal of Psychiatry, 177, 47-51. Public Library of Science – Medicine (Working Links): Lacasse JR, Leo J (2005) Serotonin and Depression: A Disconnect between the Advertisements and the Scientific Literature. PLoS Med 2(12): e392 DOI: 10.1371/journal.pmed.0020392 Ioannidis JPA (2005) Why Most Published Research Findings Are False. PLoS Med 2(8): e124 DOI: 10.1371/journal.pmed.0020124 Healy D (2006) The Latest Mania: Selling Bipolar Disorder. PLoS Med 3(4): e185 DOI: 10.1371/journal.pmed.0030185 Smith R (2005) Medical Journals Are an Extension of the Marketing Arm of Pharmaceutical Companies. PLoS Med 2(5): e138 DOI: 10.1371/journal.pmed.0020138 | |
Posted by Linda, 08:05 22 November 2006Thanks for naming Dr. Moncrieff here Joel. She's a prominent British psychiatrist who is very outspoken against drug treatments, and I have heard her on Radio Four a number of times.
The only thing I feel that people like her are lacking is help that really works for people who are desperately depressed. I emailed her and asked her if she'd heard of using nutrition as a way to heal, and she wrote back dismissing this and asking me if I exercised, which was a shame (though it was nice she took the time to reply). I took the drugs out of sheer desperation. I felt I'd tried everything else I could possibly think of, and I was suicidal. On Withdrawal and Recovery, as well as learning about the drugs and how to come off them, I learned about how to eat nutritiously. No fad diets, just nutrition, based on how we know our ancestors ate, the foods they evolved on, the foods our bodies still need in abundance. So this includes lots of veg, protein, healthy fats (i.e. fish oil, olive oil, butter), some fruit, and all of it fresh. No processed food, frozen food, and no foods that contain antinutrients. I could go into what these are if anyone is interested, but the king of all antinutrients is sugar. I have no doubt that my abuse of this substance over 34 years of my life contrinuted to the eventual depression. I've got a lot of info about the negative effects of sugar on the body, and can give it if anyone wants, but at the moment that's a whole new topic. Hand in hand with this, I am taking supplements like a top-quality multivitamin, vitamin C, colloidal minerals (to get the trace minerals largely lacking from the ground due to intensive farming -- again, I have info on this if anyone wants it), fish oil, calcium, magnesium -- well, those are the big ones. The Western diet is largely lacking in essential nutrition, and for various reasons there are fewer nutrients in our food now than there were even a generation or two ago. Could you really believe that nutritional deficiencies -- not severe enough to manifest as things like scurvy or pellagra, but deficiencies all the same -- can cause illness, including mental illness? Well I guess a lot of people would dismiss this. I'm just saying it here because it made sense to me, and focusing on nutrition in this way helped me to a significant degree, like nothing else had. This is how everyone else is asked to eat on Withdrawal and Recovery, and there are a lot of success stories there. When these psychiatrists who speak out against these drugs are ready to marry nutritional healing along with their ideas, then maybe some profound changes will start to happen. I hope I live to see the day. If anyone wants more info on anything I've mentioned here, please ask. I thought that nutrition and supplements were at least worth a mention. When a deficiency is the actual cause of mental illness, as can often be the case, then trying any other approach is likely to be met with minited success. Again, look at the example of Linus Pauling's mother, who died of pernicious anemia. She suffered years of mental illness that the doctors couldn't treat, and a vitamin would have saved her life. I'm not trying to peddle this approach to people who aren't interested. However, I thought it was worth mentioning, especially when I suggest to people that they look at their diets. This is where I'm coming from. Take it or leave it, but please think about it before you brush it off. If you've been living off a diet of junk food, starch, sugar -- or even if you just don't eat very much, and few or no vegetables -- like most of the people who end up on Withdrawal and Recovery -- then you're doing yourself a disservice if you ignore this and decide it doesn't affect your mental or physical health. | |
Posted by Patricia, 09:39 22 November 2006Having only ever tried AD's once before many years ago & having such a horrid reaction to them that I decided that no matter how bad things got there was no way I was going back onto them, I felt as though I was a zombie and my whole body shook from the minute I took the first pill, I realised when my body stopped shaking that it was the pill which had caused it, I therefore took the decision to leave them alone, as people kept asking me "are you alright?", my reply was "I am not sure".
I think the best advice a friend ever gave me was to put the pills in the bin and go from there, this might not be to everyones I don't feel we have the right to tell others how to *fix*, their lives we can only lead by example as it were. :lol: | |
Posted by Linda, 14:42 22 November 2006I guess all I can say there is thanks for the input Patricia, and in a way it's lucky you got that reaction. If you hadn't, I suppose it's likely you would have stayed on the drugs.
From the start, the most disturbing thing for me was that they numbed me inside. The anxiety went away, but so did my feelings. I just told myself, "This is what the drugs do I guess. Better get used to it." But it was awful. I wanted to leave this info here so that people could access it if they looked in the archives, because I think maybe I won't be writing here much anymore. I just don't hear anyone else here saying these things, and people need to be aware of them so that they have a better understanding of the ways in which depression can be treated. Who else would suggest to them that they may have a nutritional deficiency, or that their drugs may be their problem? Would they even have thought of that? Any good therapeutic treatment gets at the root of the problem and works from there, and I can't imagine myself ever disagreeing with an approach that does that. However drugs do not get at the root of the problem; in fact, they can obscure it and cause people to ignore it. It's a sad state of affairs when doctors are so quick to give a pill. | |
Posted by megj, 13:59 24 November 2006Some really interesting looking reading there, thanks Linda (and Joel).
I genuinely resent the 'pill for every ill' attitude that pervades western society, but equally I am amazed and proud of much of the research and development done, particularly to cure chronic and degenerative illnesses. I have to take medication every day, for my physical health, and would not be without that support for the world, but would be off it in a flash if I could - I've tried more than once to no success. I do think that lifestyle and society has a greater impact on health than many people are willing to accept. Social inclusion is a biggie too - how many of us actually live in a real community? Family and friends all nearby, knowing the shop workers and everyone on your street? Without these networks, we are all far more prone to illness (physical or mental). I'm very happy to see so much time and effort being put into social inclusion work, but sad that we need government money to keep us socially involved. A bit of a ramble I know, but I don't really have anywhere else to share this kind of thing. | |
Posted by Linda, 18:21 24 November 2006Well thanks for sharing it here Meg. I really do agree with you. Our sense of community has splintered. I feel it very keenly, as a stay-at-home mum. There are few neighbours around, few people to see. I'm going to be quitting my current job and going back to the stay-at-home thing for a while and am going to have to work really hard to avoid feeling so lonely and isolated again -- which was a big trigger for the depression I think.
BTW I feel the same about meds as you. Some of them are wonders of modern science and can help people where nothing else can. However I would never put ADs in that category. It's nice to meet someone else who is willing to look at other causes of depression. We are sold the idea that depression is an illness like cancer or diabetes. Most doctors believe this. Norman Rosenthal believes this. Not only does it suggest that the best treatment is drugs, but it also removes all responsibility for the individual to consider factors in their own life that need changing. Depression is a wake-up call that needs to be heeded for a person to be healthy -- numbing it out means ignoring the call for change and growth. Linda. | |
Posted by Linda, 12:48 26 November 2006Excerpt from "Psychopharmacology and Human Values" by Peter Breggin
http://www.breggin.com/psychopharmacologyand.pbreggin.2003.pdf Psychopharmacology and psychiatry now dominate the mental health field. Even humanistic and existential therapists are likely to refer difficult or disturbed clients to physicians, especially psychiatrists, for possible medication. The prevailing professional tendency is to conceptualise the conflict between psychotherapy and drug treatment as a scientific one; but it is at root a conflict between two different views of human nature. We need to renew our faith in the psychiatric drug-free human being in both our personal and professional lives. Throughout the mental health professions, and medicine in general, there is an increasing reliance on psychiatric drugs for a broadening array of human suffering from conflict between parents and children to anxiety and despair among adults. This professional reliance on drugs takes many forms, including (a) failure to recognise the existence of safer and more effectove psychtherapeutic approaches, (b) distrusting their own professional skills at critical moments in therapy, (c) overestimating the value of medication to relieve suffering, and, in particular, to prevent suicide, and (d) falsely communicating to patients that they cannot succeed in therapy without the addition of a medication. I have criticised the growing trend to use medicalised diagnoses and treatment with drugs and electroshock and have proposed better human services based on empathy (Breggin, 1991, 1992, 1997a, 1997b, 1998, 2001a, 2001b, 2002; Breggin & Breggin, 1994, 1998; Breggin, Breggin, & Bemack, 2002; Breggin & Cohen, 1999; Breggin & Stern, 1996). My views have drawn on traditions established by psychosocially oriented psychologists and psychiatrists, (e.g. Adler, 1969; Allport, 1955; Ansbacher & Ansbacher, 1956; Fromm, 1956; Laing, 1967; Laing & Esterson, 1970; Rogers, 1961, 1995; Sullivan, 1953; Szasz, 1987). Many other contemporary voices have also been criticising the fundamental principles of biological psychiatry from scientific, humanistic psychology, and philosophical perspectives (Armstrong, 1993; Caplan, 1995; Cohen & Cohen, 1983; Colbert, 1996; Fisher & Greenberg, 1989, 1997; Jacobs, 1995; Modrow, 1992; Mosher & Burti, 1989; Romme & Escher, 1993; Ross & Pam, 1995). Faith in "My Biochemical Imbalance" When people consider starting or stopping psychiatric drugs, they often feel as if they are facing a void or stepping off a cliff. These patients and their doctors believe that they must rely on psychiatric drugs. That is, they don't believe there are safer and potentially more effective alternatives to drugs. If they don't take the drugs, what else can they do? If they stop relying on psychiatric drugs, what will they rely on? What will they do about their suffering without their psychiatric drugs? In today's society, people who seek help from doctors seldom realise that reliance on psychiatric drugs is, at root, based on faith rather than on scientific conclusions. In particular, they don't know how flimsy the data is for supporting the most commonly used psychiatric medications, such as the newer generation of antidepressants called SSRIs, such as fluvoxamine (Prozac), paroxetine (Paxil/Seroxat), sertraline (Zoloft), and citalopram (Celexa). (See Breggin, 2001a, 2001b; Breggin & Breggin, 1994; Fisher & Greenberg, 1989, 1997.) In clinical practice, patients commonly present with one or another variation on the following scenario. Ms. Martin was 18 years old when she left an abusive, "dysfunctional" family and attempted to live alone and to work while putting herself through college. Her family actively opposed her efforts, and she eventually began to feel paralysed with anxiety and hopelessness. After returning home, the family doctor told her that she was suffering from "major depression" caused by a "biochemical imbalance." He placed her on an antidepressant that she continued to take for several years. She then suffered a brief "manic" episode that, in retrospect, was probably induced by the antidepressant. The family doctor referred Ms. Martin to a psychiatrist who reemphasised to her that she had a "biochemical imbalance" caused by genetic and biological dysfunctions. He changed her diagnosis from major depression to bipolar disorder without informing her that the antidepressant probably caused her "mania." He prescribed another antidepressant and added lithium to "stabilise" her "mood swings." For the next 10 years, Ms. Martin's life involved a constant tinkering with antidepressants, often two at a time, and various dosing schedules of lithium and other drugs. She never returned to college and enjoyed only moderate success at work compared to her real abilities. When Ms. Martin began to realise that she was becoming increasingly apathetic and experiencing memory loss, she sought help to assist her in coming off psychiatric drugs. In the initial discussions, it became apparent that Ms. Martin had been living for many years according to the simplistic faith of biopsychiatry: "I have a genetic and biological disease called bipolar disorder that requires treatment for the rest of my life. The drugs correct by biochemical imbalance." The biopsychiatric faith had left Ms. Martin dependent on doctors for medication. The drugs had confined her within the physical constraints of drug-induced emotional numbness and apathy and ultimately impaired her cognitive function. She plodded along in drug-induced stagnation without ever experiencing personal fulfillment in her work or social life. Although Ms. Martin's initial crisis developed during her teenage attempt to leave an abusive home, none of her doctors suggested to her that she might have psychologically based problems and that psychotherapy or counselling might be helpful. The biochemical bias of her doctors actively discouraged her from learning about and overcoming the original sources for her problems. Over a period of several months, Ms. Martin was able to withdraw from psychiatric drugs. In the process, she developed a philosophy of life that empowered her to take charge of her thoughts and feelings and to take new steps toward the fulfillment of her psychological, social, and creative needs. She convinced her employer to pay for her college credits, and she began a marked escalation in career achievements. She was also more able to express her feelings and to develop more fulfilling personal relationships. *********** In the humanistic, existential approach, human beings are seen as endowed with unique capacities, yearnings, and aspirations. They seek to overcome and transcend suffering through self-understanding, ethics, community, and enriched lives. In this model, people must take personal responsibility for their lives, including the quality of their mental condition and relationships with others, including children. The corresponding psychotherapeutic model does not reject the existence of the body or the attempt to address complex mind-body issues. Its emphasis is more focused and even practical: First, the human suffering dealt with by psychiatrists and other mental health professionas is almost always psychological, existential and social in nature, rather than biological; and second, psychotherapeutic rather than biological interventions are safer and more effective for these problems. When patients do turn out to have a real physical problem contributing to their psychological suffering, such as a chronic head injury or thyroid disease, they need specific medical treatments and not psychiatric drugs. There are many traditional ideas about human nature that are particularly relevant when trying to reject or to withdraw from psychiatric drugs. -- Pain and suffering have meaning. Emotions are signals, not symptoms; they tell us about our physical and psychological condition. When we blunt our emotions, we blind ourselves to our inner feelings and needs and suppress our human nature. -- Heroism is required to live a principled life in the face of the inevitable pain and suffering that all human beings endure. -- There are no short cuts to making life less painful or to achieving peace of mind. Hard work and rational, consistent principles are required to achieve a state of contentment or satisfaction, and such a state always remains fragile. -- Human beings thrive to the extent that they live by ideals and refuse to compromise them. In recent centuries, philosophy and psychology have added to concepts of human nature, the self, or the soul. Following are some of these more contemporary humanistic or existential principles: -- Individuals seek self-actualisation or self-fulfillment through the development and expression of their unique capacities and will suffer if this pursuit is inhibited or thwarted. -- Empathy -- the capacity to understand and to care about the feelings and viewpoint of others -- is central to an ethical and fulfilling life. Empathy is also the basis of healing. -- Successful people take personal repsonsibility for choosing the principles by which they conduct their lives. -- Emotional and psychological suffering can come from many causes -- from early childhood trauma to unhappiness in marriage or work. It can also come from the failure to find a meaningful way of life. Triumph over psychological suffering requires self-understanding, responsibility, and commitment to sound principles of living. Biopsychiatric Mechanical Model of Human Life When people choose to become patients of a psychiatrist who prescibes drugs, they are doing a great deal more than merely "seeing the doctor." They are subjecting themselves to a very specific and limited model of thinking about human suffering and failure. The widespread adoption of this mechanistic model is relatively new in the hisotry of humankind. It demands that we think of ourselves as broken machines or flawed mechanical devices. It requires blind faith in doctors and scientists, combined with a materialistic faith in molecular causes and manipulations. In the biopsychiatric model, we are mechanical devices similar to computers or other machines. Our suffering is caused by genetic and biological factors beyond our control. When we cannot seem to find a solution on our own, we place our fate in the hands of technicians who know how to tinker with our machinery. In this mechanical model, we have very little personal responsibility for our condition. We are spared the painful search for the personal and psychological causes of our suffering in our lives as children and adults. We are relieved of the necessity of finding more valid and meaningful principles of living. We do not have to face our conflicts with our husbands or wives, fathers or mothers, children, friends, coworkers, or bosses. We do not have to seek more meaningful work and satisfying relationships. Heroism and determination in the face of our suffering becomes irrelevant. We are only responsible for taking our medications as directed. For these reasons, the psychotherapeutic model cannot be successfully blended with the biological model. The biological model undermines the core of the humanistic, existential or psychotherapeutic approach in therapy. Taking psychiatric drugs is not like taking insulin for diabetes. In psychiatry, the "target organ" is the brain, and the brain is the seat of our thinking, feeling selves. This is very different from taking drugs to modify the functioning of our hearts or livers. Consider, for example, the difference between a heart transplant and a brain transplant. If you were to exchange your old brain for a new one, you would become another person -- the person who donated the brain. You, as a distinct person, would die with the death of your old brain. But you can exchange your heart for a new one without losing your identity and without becoming the donor. To pursue the parallel, when you take a psychiatric drug, you change yourself as a person; but when you take a cardiac drug, little about you as a person is changed. Tragically, modern, well-informed people too often put their faith in psychiatry and its drugs. This has become the equivalent of putting one's faith in the pharmaceutical industry. Drug promotion panders to the most superficial values in the culture: the hope of short cuts around the need for personal responsibility and personal growth. In doing so, the drug companies and biological psychiatry do more harm than good. Mental health professionals need to reclaim their professional knowledge and skills. They should srtive to help their clients and patients to reclaim their faith in fundamental values, including personal responsibility, empathy and love, and principled living. | |
Posted by Linda, 17:36 30 November 2006URL: http://www.msnbc.msn.com/id/15954759/
Hospital boards too closely tied to industry Panels that oversee experiments tainted by conflicts of interest, study finds The Associated Press Updated: 7:33 p.m. ET Nov 29, 2006 A survey of hospital review boards that watchdog experiments on patients shows that one in three members takes money from companies that make drugs and medical devices that come under study. What's more, many of those with conflicts rarely or never disclose their financial ties, researchers found. The study of 100 university medical centers is said to be the first to look at financial conflicts of interest on hospitals' institutional review boards. IRBs are little-known committees responsible for protecting patients in research experiments. The study's findings are alarming, said some patient advocates. If the review board "is riddled with financial conflicts of interest, it's not going to be as protective as it should be," said Dr. Sidney Wolfe, director of the Public Citizen's Health Research Group. The study was published in this week's issue of the New England Journal of Medicine. Corporate funding of medical research is common and a mainstay in the translation of scientific discoveries into medical treatments. But in the last five years, there has been heightened scrutiny of the financial ties between researchers and the companies that make experimental drugs and devices. The question: Do medical researchers always act in the best interest of science - or patients - if they are also getting royalties, consulting fees or other benefits from the makers of the products being tested? Volunteer boards All federally funded research must be reviewed and approved by IRBs, which consider patient safety as well as ethical conflicts. Most members of these boards are volunteers, usually doctors or scientists themselves, who get no extra pay for their service. They are expected to be more sensitive to ethical concerns than the researchers they monitor, said Dr. Jerome Kassirer, a former New England Journal of Medicine editor who wrote a book in 2005 on medical conflicts of interest. Now researchers are "finally getting around to looking at all the ways that pharmaceutical companies can have an adverse influence on health," Kassirer added. In the study, led by Eric Campbell of Massachusetts General Hospital and Harvard Medical School, 575 members of IRBs at 100 universities were surveyed; they were promised anonymity. About 36 percent - or more than 200 respondents - reported at least one form of industry financial ties in the previous year. Roughly 15 percent - or about 80 respondents - said that in the previous year, they were asked to review at least one research study that was sponsored by a company with which they had a relationship or by a competitor of that company. Both situations constitute a conflict of interest, the study's authors noted. Of those respondents, more than half said they always disclosed their conflict to other board members, but 35 percent said they rarely or never did. Nearly one in five said that regardless of their conflicting ties, they always voted on whether to approve the proposed clinical study. Federal regulations bar IRB members from voting in a review of a study in which they have a conflict of interest. "This (the study's results) reflect a significant lack of law enforcement," Wolfe said. Lack of awareness It may also reflect a lack of awareness, said Campbell, the lead author. Of all the study's respondents, fewer than half said their review boards had a formal written definition of what makes a conflict of interest. As for patients, a second study published in the journal, suggested that those fighting for their lives were more focused on being cured than worrying about conflicts of interest by researchers. The study, led by researchers at the National Institutes of Health, involved cancer patients enrolled in clinical trials. Most said such conflicts did not worry them, and 77 percent knew little about the issue. | |
Posted by Linda, 07:54 2 December 2006http://thestreetspirit.org/August2005/interview.htm
Psychiatric Drugs: An Assault on the Human Condition Interview by Terry Messman Bad Science, Bad Medicine, and the Enduring Mistreatment of the Mentally Ill. Investigative reporter Robert Whitaker, author of the groundbreaking book Mad In America, is now pursuing a fascinating line of research into how the mammoth psychiatric drug industry is endangering the American public by covering up the untold cases of suffering, anguish and disease caused by the most widely prescribed antidepressants and antipsychotic medications. Whitaker exposes the massive lies and cover-ups that have corrupted the Food and Drug Administration's drug review process, and co-opted research trials in order to spin the results of drug tests and conceal the serious hazards and even deadly side-effects of brand- name drugs like Prozac, Zoloft, Paxil and Zyprexa. The story becomes even more frightening when we look at the aggressive tactics these giant drug companies have used to silence prominent critics by defaming them in the press, and by using their money and power to have widely respected scientists and eminent medical researchers fired for daring to point out the hazards and risks of suicide and premature death caused by these drugs. Whitaker starts by debunking the effectiveness of these massively hyped wonder drugs -- antidepressants like Prozac, Zoloft and Paxil, and the new atypical antipsychotic drugs like Zyprexa. His research shows how they often are barely more effective than placebos in treating mental disorder and depression, despite the glowing adulation they have received in the mainstream media. But he goes on to make the startling claim that these new psychiatric drugs have directly contributed to an alarming new epidemic of drug- induced mental illness. The very drugs prescribed by physicians to stabilize mental disorders in fact are inducing pathological changes in brain chemistry and triggering suicide, manic and psychotic episodes, convulsions, violence, diabetes, pancreatic failure, metabolic diseases, and premature death. Whitaker originally was a highly regarded science reporter for the Boston Globe. When he began to research a series on psychiatric issues for the Globe, he was still a believer in the story of progress that psychiatry has been telling the public for decades. He said, "I absolutely believed the common wisdom that these antipsychotic drugs actually had improved things and that they had totally revolutionized how we treated schizophrenia. People used to be locked away forever, and now maybe things weren't great, but they were a lot better. It was a story of progress." That story of progress was fraudulent, as Whitaker soon found out when he gained new insight from his research into torturous psychiatric practices such as electroshock, lobotomy, insulin coma, and neuroleptic drugs. Psychiatrists told the public that these techniques "cured" psychosis or balanced the chemistry of the brain. But, in reality, the common thread in all these different treatments was the attempt to suppress "mental illness" by deliberately damaging the higher functions of the brain. The stunning truth is that, behind closed doors, the psychiatric establishment itself labeled these treatments as "brain-damaging therapeutics." The first generation of antipsychotic drugs created a drug-induced brain pathology by blocking the neurotransmitter dopamine and essentially shutting down many higher brain functions. In fact, when antipsychotics such as Thorazine and Haldol were first introduced, psychiatrists themselves said that these neuroleptic drugs were virtually indistinguishable from a "chemical lobotomy." In recent years, the media have heralded the arrival of so-called designer drugs like Prozac, Paxil and Zyprexa that are supposed to be superior and have fewer side effects than the old tricyclic antidepressants and the first antipsychotics. Millions of Americans have believed this story and have enriched drug companies like Eli Lilly by spending billions of dollars annually to purchase these new medications. Whitaker's research into the tragic cases of disease, suffering and early deaths caused by these drugs shows that millions of consumers have been misled by a massive campaign of lies, distortions, and bought-and-paid-for drug trials. Eminent medical researchers who have tried to warn us of the perils of these drugs have been silenced, intimidated and defamed. In the process, the Food and Drug Administration has become the lapdog of the giant pharmaceutical industry, not its watchdog. Street Spirit interviewed Robert Whitaker about this new "epidemic" of mental disorders, and how the giant drug companies have profited from selling drugs that make us sicker. Street Spirit: Your new line of research indicates that there has been an enormous rise in the incidence of mental illness in the United States, despite the seeming advances in a new generation of psychiatric drugs. Why do you refer to this increase as an epidemic? Robert Whitaker: Even people like the psychiatrist E. Fuller Torrey wrote a book recently in which he said it looks like we're having an epidemic of mental illness. When the National Institute of Mental Health publishes its figures on the incidence of mental illness, you see these rising numbers of mentally ill people. Some recent reports even say that 20 percent of Americans now are mentally ill. So what I wanted to do was two-fold. I wanted to look into exactly how dramatic is this increase in mental illness, and particularly severe mental illness. Part of this rise in the number of people said to be mentally ill is just definitional. We draw a big wide boundary today and we throw all sorts of people into that category of mentally ill. So children who are not sitting neatly enough in their school rooms are said to have attention deficit hyperactivity disorder (ADHD), and we created a new disorder called social anxiety disorder. SS: So what used to be called simply shyness or anxiety in relating to people is now labeled a mental disorder and you supposedly need an antidepressant like Paxil for social anxiety disorder. RW: Exactly. And you need a stimulant like Ritalin for ADHD. SS: This increases psychiatry's clients, but doesn't it also increase the number of people that giant pharmaceutical companies can sell their psychiatric drugs to? RW: Absolutely. So part of what we're seeing is nothing more than the creation of a larger market for drugs. If you think about it, as long as we draw as big a circle as possible, and expand the boundaries of mental illness, psychiatry can have more clients and sell more drugs. So there's a built-in economic incentive to define mental illness in as broad terms as possible, and to find ordinary, distressing emotions or behaviors that some people may not like and label them as mental illness. SS: Your research also shows that there is a real increase in people who have a severe mental disorder. Now, this seems counterintuitive, but is it true that you believe much of this increase is caused by the overuse of some of the new generations of psychiatric drugs? RW: Yes, exactly. I looked at the number of the so-called severely disabled mentally ill -- people who aren't working or who are somehow dysfunctional because of mental illness. So I wanted to chart through history the percentage of the population who are considered the disabled mentally ill. Now, by 1903, we see that roughly 1 out of every 500 people in the United States is hospitalized for mental illness. By 1955, at the start of the modern era of psychiatric drugs, roughly one out of every 300 people was disabled by mental illness. Now, let's go to 1987, the end of the first generation of antipsychotic drugs; and from 1987 forward we get the modern psychiatric drugs. From 1955 to 1987, during this first era of psychiatric drugs -- the antipsychotic drugs Thorazine and Haldol and the tricyclic antidepressants (such as Elavil and Anafranil) -- we saw the number of disabled mentally ill increase four-fold, to the point where roughly one out of every 75 persons are deemed disabled mentally ill. Now, there was a shift in how we cared for the disabled mentally ill between 1955 and 1987. In 1955, we were hospitalizing them. Then, by 1987, we had gone through social change, and we were now placing people in shelters, nursing homes, and some sort of community care, and gave them either SSI or SSDI payments for mental disability. In 1987, we started getting these supposedly better, second-generation psychiatric drugs like Prozac and the other selective serotonin re- uptake inhibitor (SSRI) antidepressants. Shortly after that, we get the new, atypical antipsychotic drugs like Zyprexa (olanzapine), Clozaril and Risperdal. What's happened since 1987? Well, the disability rate has continued to increase until it's now one in every 50 Americans. Think about that: One in every 50 Americans disabled by mental illness today. And it's still increasing. The number of mentally disabled people in the United States has been increasing at the rate of 150,000 people per year since 1987. That's an increase every day over the last 17 years of 410 people per day newly disabled by mental illness. SS: So that leads to the obvious question. If psychiatry has introduced these so-called wonder drugs like Prozac and Zoloft and Zyprexa, why is the incidence of mental illness going up dramatically? RW: That's exactly it. This is a scientific question. We have a form of care where we're using these drugs in an ever more expansive manner, and supposedly we have better drugs and they're the cornerstone of our care, so we should see decreasing disability rates. That's what your expectation would be. Instead, from 1987 until the present, we saw an increase in the number of mentally disabled people from 3.3 million people to 5.7 million people in the United States. In that time, our spending on psychiatric drugs increased to an amazing degree. Combined spending on antipsychotic drugs and antidepressants jumped from around $500 million in 1986 to nearly $20 billion in 2004. So we raise the question: Is the use of these drugs somehow actually fueling this increase in the number of the disabled mentally ill? When you look at the research literature, you find a clear pattern of outcomes with all these drugs -- you see it with the antipsychotics, the antidepressants, the anti-anxiety drugs and the stimulants like Ritalin used to treat ADHD. All these drugs may curb a target symptom slightly more effectively than a placebo does for a short period of time, say six weeks. An antidepressant may ameliorate the symptoms of depression better than a placebo over the short term. What you find with every class of these psychiatric drugs is a worsening of the target symptom of depression or psychosis or anxiety over the long term, compared to placebo-treated patients. So even on the target symptoms, there's greater chronicity and greater severity of symptoms. And you see a fairly significant percentage of patients where new and more severe psychiatric symptoms are triggered by the drug itself. SS: New psychiatric symptoms created by the very drugs people are told will help them recover? RW: Absolutely. The most obvious case is with the antidepressants. A certain percentage of people placed on the SSRIs because they have some form of depression will suffer either a manic or psychotic attack -- drug-induced. This is well recognized. So now, instead of just dealing with depression, they're dealing with mania or psychotic symptoms. And once they have a drug-induced manic episode, what happens? They go to an emergency room, and at that point they're newly diagnosed. They're now said to be bipolar and they're given an antipsychotic to go along with the antidepressant; and, at that point, they're moving down the path to chronic disability. SS: Modern psychiatry claims that these psychiatric drugs correct pathological brain chemistry. Is there any evidence to back up their claim that abnormal brain chemistry is the culprit in schizophrenia and depression? RW: This is the key thing everyone needs to understand. It really is the answer that unlocks this mystery of why the drugs would have this long-term problematic effect. Start with schizophrenia. They hypothesize that these drugs work by correcting an imbalance of the neurotransmitter dopamine in the brain. The theory was that people with schizophrenia had overactive dopamine systems; and these drugs, by blocking dopamine in the brain, fixed that chemical imbalance. Therefore, you get the metaphor that they're like insulin is for diabetes; they're fixing an abnormality. With the antidepressants, the theory was that people with depression had too low levels of serotonin; the drugs upped the levels of serotonin in the brain and therefore they're balancing the brain chemistry. First of all, those theories never arose from investigations into what was actually happening to people. Rather, they would find out that antipsychotics blocked dopamine and so they theorized that people had overactive dopamine systems. Same with the antidepressants. They found that antidepressants upped the levels of serotonin; therefore, they theorized that people with depression must have low levels of serotonin. But here is the thing that one wishes all of America would know and wishes psychiatry would come clean on: They've never been able to find that people with schizophrenia have overactive dopamine systems. They've never been able to find that people with depression have underactive serotonin systems. They've never found consistently that any of these disorders are associated with any chemical imbalance in the brain. The story that people with mental disorders have known chemical imbalances -- that's a lie. We don't know that at all. It's just something that they say to help sell the drugs and help sell the biological model of mental disorders. But the kicker is this. We do know, in fact, that these drugs perturb how these chemical messengers work in the brain. The real paradigm is: People diagnosed with mental disorders have no known problem with their neurotransmitter systems; and these drugs perturb the normal function of neurotransmitters. SS: So rather than fixing a chemical imbalance, these widely prescribed drugs distort the brain chemistry and make it pathological. RW: Absolutely. Stephen Hyman, a well-known neuroscientist and the former director of the National Institute of Mental Health, wrote a paper in 1996 that looked at how psychiatric drugs affect the brain. He wrote that all these drugs create perturbations in neurotransmitter functions. And he notes that the brain, in response to this drug from the outside, alters its normal functions and goes through a series of compensatory adaptations. In other words, it tries to adapt to the fact that an antipsychotic drug is blocking normal dopamine functions. Or in the case of antidepressants, it tries to compensate for the fact that you're blocking a normal reuptake of serotonin. The way it does this is to adapt in the opposite way. So, if you're blocking dopamine in the brain, the brain tries to put out more dopamine and it actually increases the number of dopamine receptors. So a person placed on antipsychotic drugs will end up with an abnormally high number of dopamine receptors in the brain. If you give someone an antidepressant, and that tries to keep serotonin levels too high in the brain, it does exactly the opposite. It stops producing as much serotonin as it normally does and it reduces the number of serotonin receptors in the brain. So someone who is on an antidepressant, after a time ends up with an abnormally low level of serotonin receptors in the brain. And here's what Hyman concluded about this: After these changes happened, the patient's brain is functioning in a way that is "qualitatively as well as quantitatively different from the normal state." So what Stephen Hyman, former head of the NIMH, has done is present a paradigm for how these drugs affect the brain that shows that they're inducing a pathological state. SS: So the paradox is there's no evidence for modern psychiatry's claim that there is any pathological biochemical imbalance in the brain that causes mental illness, but if you treat people with these new wonder drugs, that is what creates a pathological imbalance? RW: Yes, these drugs disrupt normal brain chemistry. That's the real paradox here. And the real tragedy is, that even as we peddle these drugs as chemical balancers, chemical fixers, in truth we're doing precisely the opposite. We're taking a brain that has no known abnormal brain chemistry, and by placing people on the drugs, we're perturbing that normal chemistry. Here's how Barry Jacobs, a Princeton neuroscientist, describes what happens to a person given an SSRI antidepressant. "These drugs," he said, "alter the level of synaptic transmission beyond the physiologic range achieved under normal environmental biological conditions. Thus, any behavioral or physiologic change produced under these conditions might more appropriately be considered pathologic rather than reflective of the normal biological role of serotonin." SS: One of the SSRI antidepressants that's widely believed to be a wonder drug is Prozac. Yet your research found that the Food and Drug Administration (FDA) received more adverse reports about Prozac than any other drug. What sort of ill effects were people reporting? RW: First of all, with Prozac and the SSRIs that followed, their level of efficacy was always of a very minor sort. In all the clinical trials of the antidepressants, roughly 41 percent of the patients got better in the short term versus 31 percent of the patients on placebo. Now just one other caveat on that. If you use an active placebo in these trials -- an active placebo causes a physiologic change with no benefit, like a dry mouth -- any difference in outcome between the antidepressant and placebo virtually disappears. SS: Weren't the early drug tests of Prozac so unpromising that they had to manipulate test results to get FDA approval at all? RW: What happened with Prozac is a fascinating story. Right from the beginning, they noticed only very marginal efficacy over placebo; and they noticed that they had some problems with suicide. There were increased suicidal responses compared to placebo. In other words, the drugs was agitating people and making people suicidal who hadn't been suicidal before. They were getting manic responses in people who hadn't been manic before. They were getting psychotic episodes in people who hadn't been psychotic before. So you were seeing these very problematic side effects even at the same time that you were seeing very modest efficacy, if any, over placebo in ameliorating depression. Basically, what Eli Lilly (Prozac's manufacturer) had to do was cover up the psychosis, cover up the mania; and, in that manner, it was able to get these drugs approved. One FDA reviewer even warned that Prozac appeared to be a dangerous drug, but it was approved anyway. We're seemingly finding all this out only now: "Oh, Prozac can cause suicidal impulses and all these SSRIs may increase the risk of suicide." The point is, that wasn't anything new. That data was there from the very first trial. You had people in Germany saying, "I think this is a dangerous drug." SS: Even back in the late 1980s, they already knew? RW: Before the late 1980s -- in the early '80s, before Prozac gets approved. Basically what Eli Lilly had to do was cover up that risk of mania and psychosis, cover up that some people were becoming suicidal because they were getting this nervous agitation from Prozac. That's the only way it got approved. There were various ways they did the cover-up. One was just to simply remove reports of psychosis from some of the data. They also went back and recoded some of the trial results. Let's say someone had a manic episode or a psychotic episode; instead of putting that down, they would just put down a return of depression, and that sort of thing. So there was a basic need to hide these risks right from the beginning, and that's what was done. So Prozac gets approved in 1987, and it's launched in this amazing PR campaign. The pill itself is featured on the cover of several magazines! It's like the Pill of the Year . And it's said to be so much safer: a wonder drug. We have doctors saying, "Oh, the real problem with this drug is that we can now create whatever personality we want. We're just so skilled with these drugs that if you want to be happy all the time, take your pill!" That was complete nonsense. The drugs were barely better than placebo at alleviating depressive symptoms over the short term. You had all these problems; yet we were touting these drugs, saying, "Oh, the powers of psychiatry are such that we can give you the mind you want - - a designer personality!" It was absolutely obscene. Meanwhile, which drug, after being launched, quickly became the most complained about drug in America? Prozac! SS: What were the level of complaints when Prozac hit the market? RW: In this county, we have Medwatch, a reporting system in which we report adverse events about psychiatric drugs to the FDA. By the way, the FDA tries to keep these adverse reports from the public. So, instead of the FDA making these easily available to the public. so you can know about the dangers of the drugs, it's very hard to get these reports. Within one decade, there were 39,000 adverse reports about Prozac that were sent to Medwatch. The number of adverse events sent to Medwatch is thought to represent only one percent of the actual number of such events. So, if we get 39,000 adverse event reports about Prozac, the number of people who have actually suffered such problems is estimated to be 100 times as many, or roughly four million people. This makes Prozac the most complained about drug in America, by far. There were more adverse event reports received about Prozac in its first two years on the market than had been reported on the leading tricyclic antidepressant in 20 years. Remember, Prozac is pitched to the American public as this wonderfully safe drug, and yet what are people complaining about? Mania, psychotic depression, nervousness, anxiety, agitation, hostility, hallucinations, memory loss, tremors, impotence, convulsions, insomnia, nausea, suicidal impulses. It's a wide range of serious symptoms. And here's the kicker. It wasn't just Prozac. Once we got the other SSRIs on the market, like Zoloft and Paxil, by 1994, four SSRI antidepressants were among the top 20 most complained about drugs on the FDA's Medwatch list. In other words, every one of these drugs brought to market started triggering this range of adverse events. And these were not minor things. When you talk about mania, hallucinations, psychotic depression, these are serious adverse events. Prozac was pitched to the American public as a wonder drug. It was featured on the covers of magazines as so safe, and as a sign of our wonderful ability to effect the brain just as we want it. In truth, the reports were showing it could trigger a lot of dangerous events, including suicide and psychosis. The FDA was being warned about this. They were getting a flood of adverse event reports, and the public was never told about this for the longest period of time. It took a decade for the FDA to begin to acknowledge the increased suicides and the violence it can trigger in some people. It just shows how the FDA betrayed the American people. This is a classic example. They betrayed their responsibility to act as a watchdog for the American people. Instead they acted as an agency that covered up harm and risk with these drugs. SS: In light of the FDA's failure to warn us about Prozac, what about their recent negligence on the issue of the risk of suicide in children given antidepressants like Paxil? Weren't England's mental health officials far better than their American counterparts in the FDA in warning about the dangers of suicidal attempts when antidepressants are given to youth? RW: Yes. The children's story is unbelievably tragic. It's also a really sordid story. Let's go back a little to see what happened to children and antidepressants. Prozac comes to market in 1987. By the early 1990s, the pharmaceutical companies making these drugs are saying, "How do we expand the market for antidepressants?" Because that's what drug companies do -- they want to get to an ever-larger number of people. They saw they had an untapped market in kids. So let's start peddling the drugs to kids. And they were successful. Since 1990, the use of antidepressants in kids went up something like seven-fold. They began prescribing them willy-nilly. Now, whenever they did pediatric trials of antidepressants, they found that the drugs were no more effective on the target symptom of depression than placebo. This happened again and again in the pediatric drug trials of antidepressants. So, what that tells you is there is no real therapeutic rationale for the drugs because in this population of kids, the drugs don't even curb the target symptoms over the short term any better than placebo; and yet they were causing all sorts of adverse events. For example, in one trial, 75 percent of youth treated with antidepressants suffered an adverse event of some kind. In one study by the University of Pittsburgh, 23 percent of children treated with an SSRI developed mania or manic-like symptoms; an additional 19 percent developed drug-induced hostility. The clinical results were telling you that you didn't get any benefit on depression; and you could cause all sorts of real problems in kids -- mania, hostility, psychosis, and you may even stir suicide. In other words, don't use these drugs, right? It was absolutely covered up. SS: How was it covered up? RW: We had psychiatrists -- some of those obviously getting money from the drug companies -- saying the kids are under-treated and they're at risk of suicide and how could we possibly treat kids without these pills and what a tragedy it would be if we couldn't use these antidepressants. Finally, a prominent researcher in England, David Healy, started doing his own research on the ability of these drugs to stir suicide. He also managed to get access to some of the trial results and he blew the whistle. He first blew the whistle in England and he presented this data to the review authorities there. And they saw that it looks like these drugs are increasing the risk of suicide and there are really no signs of benefits on the target symptoms of depression. So they began to move there to warn doctors not to prescribe these drugs to youth. What happens in the United States? Well, it's only after there's a lot of pressure put on the FDA that they even hold a hearing. The FDA sort of downplays the risk of these drugs. They're slow to even put black box warnings on them. Why? Aren't kids lives worth protecting? If we know that we have a scientifically shown risk that these drugs increase suicide, shouldn't you at least warn about it? But the FDA was even digging in its heels about putting that black box warning on the drugs. SS: If Prozac is the nation's most complained about drug, if Paxil is shown to be a suicide risk for youth, how do these antidepressants continue to have a reputation as near-magic cures for depression? And why did the FDA failed to warn us about Paxil and Prozac for such a long time? RW: There's a couple reasons for that. The FDA's funding changed in the 1990s. An act was passed in which a lot of the FDA's funding came from the drug industry: the PDUFA Act, or Prescription Drug User Fee Act. Basically, when drug companies applied for FDA approval they had to pay a fee. Those fees became what is funding a large portion of the FDA's review of drug applications. So all of a sudden, the funding is coming from the drug industry; it's no longer coming from the people. As that act comes up for renewal, basically the drug lobbyists are telling the FDA that their job is no longer to be critically analyzing drugs, but to approve drugs quickly. And that was part of Newt Gingrich's thing: Your job is to get these drugs to market. Start partnering with the drug industry and facilitating drug development. We lost this idea that the FDA had a watchdog role. Also, in a human way, a lot of people who work for the FDA leave there and end up going to work for the drug companies. The old joke is that the FDA is sort of like a showcase for a future job in the drug industry. You go there, you work awhile, then you go off into the drug industry. Well, if that's the progression that people make, in essence they're making good old boy network connections, so they're not going to be so harsh on the drug companies. So, that's what really happened in the 1990s. The FDA was given new marching orders. The orders were: "Facilitate getting drugs to market. Don't be too critical. And, in fact, if you want to keep your funding, which was coming now from the drug industry, make sure you take these lessons to heart." SS: So the giant pharmaceutical companies have a vast amount of power to cook the results of drug tests and make researchers and even the FDA itself bow to their will? RW: The FDA, in essence, was kneecapped in the early 1990s, and we really saw it with the psychiatric drugs. The FDA became a lapdog for the pharmaceutical industry, not a watchdog. It's only now that this has become common knowledge. We have Marcia Angell, the former editor of the New England Journal of Medicine, write a book in which she says that the FDA became a lapdog. It's basically now well recognized that you had this decline and fall. As the editor of the New England Journal of Medicine, the most prestigious medical journal we have, Marcia Angell is someone who was at the very heart of American medicine, and she concluded that the FDA let down the American people. And she lost her job at the New England Journal of Medicine for starting to criticize pharmaceutical companies. She was the editor of the journal in the late 1990s and there was a corresponding doctor named Thomas Bodenheimer who decided to write an article about how you couldn't even trust what was published in the medical journals anymore because of all the spinning of results. So they did an investigation about how the pharmaceutical companies are funding all the research and spinning the trial results, so you can no longer really trust what you read in scientific journals. They pointed out that when they tried to get an expert to review the scientific literature related to antidepressants, they basically couldn't find someone who hadn't taken money from the drug companies. Now, the New England Journal of Medicine is published by the Massachusetts Medical Society which publishes a lot of other journals, and they get a lot of pharmaceutical advertising. So what happens after that article appears by Thomas Bodenheimer and an accompanying editorial by Marcia Angell about the sorry state of American medicine because of this? They both lose their jobs! She's gone and so is Thomas Bodenheimer. Think about this. We have the leading medical journal firing people, letting them go, because they dared to criticize the dishonest science and the dishonest process that was poisoning the scientific literature. So we have the FDA that's acting as lapdogs. You can't trust the scientific literature. All this shows how the American public was betrayed and didn't know about all the problems with these drugs and why it was kept from them. It has to do with money, prestige and old boy networks. SS: It also has to do with the silencing of critics. Eli Lilly uses the media to trumpet Prozac's benefits and gives perks to doctors to attend conferences to hear about its benefits, and buys off researchers. But don't they also use their power and money to silence their critics? RW: An example is Dr. Joseph Glenmullen, a psychiatrist who also works for Harvard University Health Services, and who wrote a book called Prozac Backlash to warn about the dangers of Prozac. He's finding that the drugs are being overused and cause severe side effects. He even raises questions about long-term memory problems with the drugs and cognitive dysfunction. Well, Eli Lilly then mounted a public relations campaign to try to discredit him. They sent out notices to the media questioning his affiliation with Harvard Medical School, etc. It was all about silencing the critics. If you sing the tune that the drug companies want, at the very top levels, you get paid a lot of money to fly around and give presentations about the wonders of the drugs. And those who come, and don't ask any embarrassing questions, get the lobster dinners and maybe they get a little honorarium for attending this educational meeting. So if you want to be part of this gravy train, you can. You sing the wonders of the drug, and you don't talk about their nasty side effects, and you can get a nice payment as one of their guest speakers, as one of their experts. But if you're one of the ones saying, "What about the mania, what about the psychosis?" -- they do silence you. Look at what happened to David Healy. Healy is even the best example. David Healy has this sterling reputation in England. He's written several books on the history of psychopharmacology. He's like the former Secretary of the Psychopharmacology Association over there. He gets offered a job at the University of Toronto to head up their psychiatry department. So while he's waiting to assume that position at the University of Toronto, he goes to Toronto and delivers a talk on the elevated risk of suicide with Prozac and some of the other SSRIs. By the time he's back home, the job offer has been rescinded. Now does Eli Lilly donate some money to the University of Toronto? Absolutely. So, to answer your question, yes, Eli Lilly silences dissenters as well. SS: What is the story behind the secret settlement between Eli Lilly and the survivors who sued the company after Joseph Wesbecker shot 20 coworkers after being put on Prozac? RW: During this trial in which Eli Lilly was being sued, the judge was going to allow some very damaging evidence showing wrongdoing by Eli Lilly in a previous instance. The judge said, "Go ahead and introduce this at the trial." But next thing you know, they don't introduce this; and in fact, all of a sudden, the plaintiffs no longer are presenting very damaging evidence to make their case. So the judge wonders why they are not presenting their best case anymore. He smells a rat. He suspects Eli Lilly has settled with the plaintiffs secretly and the deal is that, as part of this settlement, the plaintiffs will go ahead with a sham trial so that Eli Lilly will win the trial. Then Eli Lilly can claim, "See our drug doesn't cause people to become violent." And, indeed, that's what happened. Eli Lilly felt it was going to lose this trial. They went to the plaintiffs and said they would give them a lot of money. They agreed to go ahead and settle the case, but had the plaintiffs go ahead with the trial. That way Eli Lilly can publicly claim that they won the trial and Prozac doesn't cause harm. SS: How did this even come out into the light of day? RW: We would never have known about this except for two things. One, believe it or not, the judge, in essence, appealed the decision in his own court. He said, "I smell a rat." And through that, he found out that there was this secret settlement and that it was a sham proceeding that continued on. He said it was one of the worst violations of the integrity of the legal process that he'd ever seen. And second, an English journalist named John Cornwell wrote a book called Power to Harm: Mind, Medicine, and Murder on Trial. He wrote about this case, and yet in the United States, we got almost no news about this secret settlement and this whole perversion of the legal process. It was an English journalist who was exposing this story. My point here is this: They silence people like Marcia Angell. They pervert the scientific process. They pervert the legal process. They pervert the FDA drug review process. It's everywhere! And that's how we as a society end up believing in these psychiatric drugs. You asked the question a while back, "Why do we still believe in Prozac?" One of the reasons is that the story about Prozac is, in effect, maintained. It's publicly maintained because we do all this silencing along all these lines. The other thing to remember is that some people on Prozac do feel better. That's true. That shows up, just in the same way that some people on placebos feel better. And those are the stories that get repeated: "Oh, I took Prozac and I'm feeling better." It's that select group that does better that becomes the story that is told out there, and the story that the public hears. So that's why we continued to believe in the story of these wonder drugs that are very safe in spite of all this messy stuff that gets covered up. SS: Let's now move from the antidepressants like Prozac to consider another new group of supposed wonder drugs -- the new antipsychotic drugs. You write that long-term use of antipsychotic drugs -- both the original neuroleptic drugs like Thorazine and Haldol and the newer atypicals like Zyprexa and Risperdal -- cause pathological changes in the brain that can lead to a worsening of the symptoms of mental illness. What changes in brain chemistry result from the antipsychotics, and how can that lead to the most frightening prospect you describe -- chronic mental illness that is locked in by these drugs? RW: This is a line of research that goes across 40 years. This problem of chronic illness shows up time and time again in the research literature. This biological mechanism is somewhat well understood now. The antipsychotics profoundly block dopamine receptors. They block 70-90 percent of the dopamine receptors in the brain. In return, the brain sprouts about 50 percent extra dopamine receptors. It tries to become extra sensitive. So in essence you've created an imbalance in the dopamine system in the brain. It's almost like, on one hand, you've got the accelerator down -- that's the extra dopamine receptors. And the drug is the brake trying to block this. But if you release that brake, if you abruptly go off the drugs, you now do have a dopamine system that's overactive. You have too many dopamine receptors. And what happens? People that go abruptly off of the drug, do tend to have severe relapses. SS: So people that have been treated with these antipsychotic drugs have a far greater tendency to relapse, and have new episodes of mental illness, as opposed to people who have had other kinds of non- drug therapies? RW: Absolutely, and that was understood by 1979, that you were actually increasing the underlying biological vulnerability to the psychosis. And by the way, we sort of understood that if you muck with the dopamine system, that you could cause some symptoms of psychosis with amphetamines. So if you give someone amphetamines enough, they're at increased risk of psychosis. This is well known. And what do amphetamines do? They release dopamine. So there is a biological reason why, if you're mucking up the dopamine system, you're increasing the risk of psychosis. That's in essence what these antipsychotic drugs do, they muck up the dopamine system. Here's just one real powerful study on this: Researchers with the University of Pittsburgh in the 1990s took people newly diagnosed with schizophrenia, and they started taking MRI pictures of the brains of these people. So we get a picture of their brains at the moment of diagnosis, and then we prepare pictures over the next 18 months to see how those brains change. Now during this 18 months, they are being prescribed antipsychotic medications, and what did the researchers report? They reported that, over this 18-month period, the drugs caused an enlargement of the basal ganglia, an area of the brain that uses dopamine. In other words, it creates a visible change in morphology, a change in the size of an area of the brain, and that's abnormal. That's number one. So we have an antipsychotic drug causing an abnormality in the brain. Now here's the kicker. They found that as that enlargement occurred, it was associated with a worsening of the psychotic symptoms, a worsening of negative symptoms. So here you actually have, with modern technology, a very powerful study. By imaging the brain, we see how an outside agent comes in, disrupts normal chemistry, causes an abnormal enlargement of the basal ganglia, and that enlargement causes a worsening of the very symptoms it's supposed to treat. Now that's actually, in essence, a story of a disease process -- an outside agent causes abnormality, causes symptoms... SS: But in this case, the outside agent that triggers the disease process is the supposed cure for the disease! The psychiatric drug is the disease-causing agent. RW: That's exactly right. It's a stunning, damning finding. It's the sort of finding you would say, "Oh Christ, we should be doing something different." Do you know what those researchers got new grants for, after they reported that? SS: No, what? You'd guess they got funding to carry out these same studies on other classes of psychiatric drugs. RW: They got a grant to develop an implant, a brain implant, that would deliver drugs like Haldol on a continual basis! A grant to develop a drug delivery implant so you could implant this in the brains of people with schizophrenia and then they wouldn't even have a chance not to take the drugs! SS: Unbelievable. Designing an implant to provide a constant dose of a drug that they had just discovered causes pathology in the brain chemistry. RW: Right, they had just found that they're causing a worsening of symptoms! So why would you go on to a design a permanent implant? Because that's where the money was. And no one wanted to deal with this horrible finding of an enlargement of the basal ganglia caused by the drugs, and that is associated with the worsening of symptoms. No one wanted to deal with the fact that when you look at people medicated on antipsychotics, you start to see a shrinking of the frontal lobes. No one wants to talk about that either. They stopped that research. SS: What other side effects are caused by prolonged use of these antipsychotic drugs? RW: Oh, you get tardive dyskinesia, a permanent brain dysfunction; and akathisia, which is this incredible nervous agitation. You're just never comfortable. You want to sit but you can't sit. It's like you're crawling out of your own skin. And it's associated with violence, suicide and all sorts of horrible things. SS: Those kinds of side-effects were notorious with the first generation of antipsychotic drugs, like Thorazine, Haldol and Stelazine. But, just as with Prozac, so many people are still touting the new generation of atypical antipsychotics -- Zyprexa, Clozaril and Risperdal -- as wonder drugs that control mental illness with far fewer side effects. Is that true? What have you found? RW: No, it's just complete nonsense. In fact, I think the newer drugs will eventually be seen as more dangerous than the old drugs, if that's possible. As you know, the standard neuroleptics like Thorazine and Haldol have had quite a litany of harm with the tardive dyskinesia and all. So when we got the new atypical drugs, they were touted as so much safer. But with these new atypicals, you get all sorts of metabolic dysfunctions. Let's talk about Zyprexa. It has a different profile. So it may not cause as much tardive dyskinesia. It may not cause as many Parkinsonian symptoms. But it causes a whole range of new symptoms. So, for example, it's more likely to cause diabetes. It's more likely to cause pancreatic disorders. It's more likely to cause obesity and appetite-disregulation disorders. In fact, researchers in Ireland reported in 2003 that since the introduction of the atypical antipsychotics, the death rate among people with schizophrenia has doubled. They have done death rates of people treated with standard neuroleptics and then they compare that with death rates of people treated with atypical antipsychotics, and it doubles. It doubles! It didn't reduce harm. In fact, in their seven-year study, 25 of the 72 patients died. SS: What were the causes of death? RW: All sorts of physical illnesses, and that's part of the point. You're getting respiratory problems, you're getting people dying of incredibly high cholesterol counts, heart problems, diabetes. With olanzapine (Zyprexa), one of the problems is that you're really screwing up the core metabolic system. That's why you get these huge weight gains, and you get the diabetes. Zyprexa basically disrupts the machine that we are that processes food and extracts energy from that food. So this very fundamental thing that we humans do is disrupted, and at some point you just see all these pancreatic problems, faulty glucose regulation, diabetes, etc. That's really a sign that you're mucking with something very fundamental to life. SS: There's supposedly an alarming increase in mental illness being diagnosed in children. Millions are diagnosed with depression, bipolar and psychotic symptoms, attention deficit hyperactivity disorder, and social anxiety disorder. Is this explosive new prevalence of mental illness among children a real increase, or is it a marketing campaign that enriches the psychiatric drug industry, a bonanza for the pharmaceutical corporations? RW: You're touching on something now that is a tragic scandal of monumental proportions. I talk sometimes to college classes, psychology classes. You cannot believe the percentage of youth who have been told they were mentally ill as kids, that something was wrong with them. It's absolutely phenomenal. It's absolutely cruel to be telling kids that they have these broken brains and mental illnesses. There's two things that are happening here. One, of course, is that it's complete nonsense. As you remember as a kid, you have too much energy or you behave sometimes in not altogether appropriate ways, and you do have these extremes of emotions, especially during your teenage years. Both children and teenagers can be very emotional. So one thing that's going on is that they take childhood behaviors and start defining behaviors they don't like as pathological. They start defining emotions that are uncomfortable as pathological. So part of what we're doing is pathologizing childhood with straight-out definition stuff. We're pathologizing poverty among kids. For example, if you're a foster kid, and maybe you drew a bad straw in the lottery of life and are born into a dysfunctional family and you get put into foster care, do you know what happens today? You pretty likely are going to get diagnosed with a mental disorder, and you're going to be placed on a psychiatric drug. In Massachusetts, it's something like 60 to 70 percent of kids in foster care are now on psychiatric drugs. These kids aren't mentally ill! They got a raw deal in life. They ended up in a foster home, which means they were in a bad family situation, and what does our society do? They say: "You have a defective brain." It's not that society was bad and you didn't get a fair deal. No, the kid has a defective brain and has to be put on this drug. It's absolutely criminal. Let's talk about bipolar disorder among kids. As one doctor said, that used to be so rare as to be almost nonexistent. Now we're seeing it all over. Bipolar is exploding among kids. Well, partly you could say that we're just slapping that label on kids more often; but in fact, there is something real going on. Here's what's happening. You take kids and put them on an antidepressant -- which we never used to do -- or you put them on a stimulant like Ritalin. Stimulants can cause mania; stimulants can cause psychosis. SS: And antidepressants can also cause mania, as you pointed out. RW: Exactly, so the kid ends up with a drug-induced manic or psychotic episode. Once they have that, the doctor at the emergency room doesn't say, "Oh, he's suffering from a drug-induced episode." He says he's bipolar. SS: Then they give him a whole new drug for the mental disorder caused by the first drug. RW: Yeah, they give him an antipsychotic drug; and now he's on a cocktail of drugs, and he's on a path to becoming disabled for life. That's an example of how we're absolutely making kids sick. SS: It's like society or their schools are trying to make them manageable and they end up putting them on a chemical roller coaster against their will. RW: Absolutely. SS: There's an astonishing number of kids being given Ritalin to cure hyperactivity. But what 10-year-old boy in a confined school setting isn't hyperactive? You write that the effect of Ritalin on the dopamine system is very similar to cocaine and amphetamines. RW: Ritalin is methylphenidate. Now methylphenidate affects the brain in exactly the same way as cocaine. They both block a molecule that is involved in the reuptake of dopamine. SS: So they both increase the dopamine levels in the brain? RW: Exactly. And they do it with a similar degree of potency. So methylphenidate is very similar to cocaine. Now, one difference is whether you're snorting it or if it's in a pill. That partly changes how quickly it's metabolized. But still, it basically affects the brain in the same way. Now, methylphenidate was used in research studies to deliberately stir psychosis in schizophrenics. Because they knew that you could take a person with a tendency towards psychosis, give them methylphenidate, and cause psychosis. We also knew that amphetamines, like methylphenidate, could cause psychosis in people who had never been psychotic before. So think about this. We're giving a drug to kids that is known to have the possibility of stirring psychosis. Now, the odd thing about methylphenidate and amphetamines is that, in kids, they sort of have a counterintuitive effect. What does speed do in adults? It makes them more jittery and hyperactive. For whatever reasons, in kids amphetamines will actually still their movements; it will actually keep them in their chairs and make them more focused. So you've got kids in boring schools. The boys are not paying attention and they're diagnosed with ADHD and put on a drug that is known to stir psychosis. The next thing you know, a fair number of them are not doing well by the time they're 15, 16, 17. Some of those kids talk about how when you're on these drugs for the long term, you start feeling like a zombie; you don't feel like yourself. SS: Hollowed-out, blunted emotions. And this is being done to millions of kids. RW: Millions of kids! Think about what we're doing. We're robbing kids of their right to be kids, their right to grow, their right to experience their full range of emotions, and their right to experience the world in its full hue of colors. That's what growing up is, that's what being alive is! And we're robbing kids of their right to be. It's so criminal. And we're talking about millions of kids who have been affected this way. There are some colleges where something like 40 to 50 percent of the kids arrive with a psychiatric prescription. SS: It looks like a huge social-control mechanism. Society gives kids Ritalin and antidepressants to subdue them and make them conform. On the one hand, it's all about social control and conformity. But it also has a huge marketing payoff. RW: You're right, it creates customers for the drugs, and hopefully lifelong customers. That's what they're told, aren't they? They're told they are going to be on these drugs for life. And next thing they know, they're on two or three or four drugs. It's brilliant from the capitalist point of view. It does serve some social-control function. But you take a kid, and you turn them into a customer, and hopefully a lifelong customer. It's brilliant. We now spend more on antidepressants in this country than the Gross National Product of mid-sized countries like Jordan. It's just amazing amounts of money. The amount of money we spend on psychiatric drugs in this country is more than the Gross National Product of two- thirds of the world's countries. It's just this incredibly lucrative paradigm of the mind that you can fix chemical imbalances in the brain with these drugs. It works so well from a capitalistic point of view for Eli Lilly. When Prozac came to market, Eli Lilly's value on Wall Street, its capitalization, was around 2 billion dollars. By the year 2000, the time when Prozac was its number-one drug, its capitalization reached 80 billion dollars -- a forty-fold increase. So that's what you really have to look at if you want to see why drug companies have pursued this vision with such determination. It brings billions of dollars in wealth in terms of increased stock prices to the owners and managers of those companies. It also benefits the psychiatric establishment that gets behind the drugs; they do well by this. There's a lot of money flowing in the direction of those that will embrace this form of care. There's advertisements that enrich the media. It's all a big gravy train. Unfortunately, the cost is dishonesty in our scientific literature, the corruption of the FDA, and the absolute harm done to children in this country drawn into this system, and an increase of 150,000 newly disabled people every year in the United States for the last 17 years. That's an incredible record of harm done. SS: Everyone gets rich -- the drug companies, the psychiatrists, the researchers, the advertising agencies -- and the clients get drugged out of their minds and damaged for life. RW: And you know what's interesting? No one says that the mental health of the American people is getting better. Instead, everyone says we have this increasing problem They blame it on the stresses of modern life or something like that, and they don't want to look at the fact that we're creating mental illness. | |
Posted by Linda, 11:55 6 December 2006SSRI Experts Head to Washington to Testify Before FDA Panel
by Evelyn Pringle On December 13, 2006, the FDA's Psychopharmacologic Drugs Advisory Committee will hold a public hearing to review the suicidality data from the adult selective serotonin reuptake inhibitor (SSRI) studies. And, for what seems like the umpteenth time, SSRI experts from all over the US, and as far away as the UK, will travel to Washington to once again testify at yet another hearing on the suicide risks associated with these drugs. The committee is expected to vote on whether the risk of SSRI-induced suicidality in adults should be included in a Black Box warning on all SSRI labels, including Paxil, Prozac, Zoloft, Lexapro, and Celexa. The FDA should begin the hearing by announcing that suicide rates for adults have not declined at all in the US even with the massive wide- spread use of SSRIs. According to a Federal study, by researchers from Harvard Medical School and elsewhere, in the June 2005, Journal of the American Medical Association, despite a dramatic increase in treatment with antidepressants in 2001-2003, when compared to 1990- 1992, the rates of suicidal ideation, gestures and attempts among adults have remained basically unchanged. There is probably no legal expert in the US more qualified to testify about SSRIs than Baum Hedlund attorney, Karen Barth-Menzies, and she will be at the hearing with bells on. Over the past 10 years, she has represented thousands of clients against SSRI makers. By now, the FDA knows that Ms Menzies makes no secret of the fact that she is outraged about the over-prescribing of these powerful and dangerous drugs to all age groups for nothing more than everyday problems. This will be Ms Menzies' fourth time up to bat. She has already testified three times at government hearings. She first spoke at an FDA Psychopharmacologic Drugs and Pediatric Advisory Committee hearing in February 2004, about the increased risk of suicide in children and adolescents taking SSRIs. At that particular hearing, the famous SSRI litigator concluded her testimony by telling the panel: "Put me out of business for the right reasons. Warn about these drugs." Many of Baum Hedlund's clients who have suffered tragedies caused by SSRIs will be also be attending the hearing and some will be speaking. However, a number of clients who wanted to testify were not selected by the FDA's new "lottery" system, and will not be permitted to speak. But Ms Menzies says she plans to speak on their behalf. She has first-hand knowledge of how the drug companies hid the evidence about the suicide risks. The documents that have been unearthed in litigation reveal that the risk was known in the mid- 1980's before the first SSRI, Prozac, was approved for use in the US. Because of Baum Hedlund's work in the Prozac litigation, Ms Menzies has the ability to provide the committee with the historical background on SSRIs, including internal company documents that show how and why the SSRI suicide risk with adults was obfuscated fifteen years ago during the first FDA advisory committee hearings on the suicide issue. She will explain exactly how the clinical trial data was manipulated by SSRI makers to skew the statistical analyses of suicidality. "Civil lawsuits," she says, "have uncovered internal company documents to which not even the FDA has access." And she maintain that the drug makers have purposely failed to conduct studies on the risk of suicidality because they already knew such trials would produce negative results. In August 2004, Ms Menzies testified before the California State Senate and called for better patient informed consent about the risks associated with SSRIs. Next, she testified at the September 2004, FDA Advisory Committee's follow-up hearings and discussed the lack of efficacy in SSRI treatment of children, as documented in pediatric clinical trials that had surfaced during litigation. In between the February and September 2004 hearings, Ms Menzies met with members of Congress to discuss SSRI related suicidality and the FDA's failure to alert the public about the dangers of SSRIs, and provided documentary evidence to show that the risks posed were real. She also provided information to investigators in two separate Congressional investigations that resulted in two hearings in 2004, at which drug company executives and FDA officials were interrogated and chastised by members of Congress. In addition to Ms Menzies, one of the world's most highly regarded SSRI experts, Dr David Healy, a professor at North Wales Department of Psychological Medicine, at Cardiff University, will be flying in from the UK to testify at the hearing. He too will give a repeat performance. Dr Healy has authored 12 books including, Let Them Eat Prozac, The Antidepressant Era, and The Creation of Psychopharmacology, and is known to be outspoken when he believes it is necessary. During his testimony at this hearing, Dr Healy says he plans to draw attention to the manipulation of the clinical trial data on SSRIs. For over a decade, he has been trying to raise awareness about the link between SSRIs and suicide. Back in August 1991, Dr Healy authored the paper, "Antidepressant Induced Suicidal Ideation," in which he said that the cases of two patient "suggest that the emergence of suicidal ideation on antidepressants cannot always be attributed to a lifting of psychomotor retardation but rather that the ideas may in some instances be produced by antidepressants." Three years later in 1994, he authored the paper, "The Fluoxetine and Suicide Controversy," and stated, "In the opinion of this author, the volume of case reports and other studies is sufficient to demonstrate that antidepressants and antipsychotics may induce suicidal ideation in certain individuals under certain conditions." After the February 2004 advisory committee hearings, Dr Healy analyzed the data from the pediatric SSRI trials on suicidality and hostility, including those kept hidden for years, and sent his analysis to the FDA on February 19, 2004. To distinguish the difference between suicide possibly caused by SSRIs verses suicide caused by an underlying illness of depression, Dr Healy broke down the studies into a group of children being treated for depression and a group of anxious children who were being treated for obsessive compulsive disorder or social phobia. From a pool of 931 depressed patients taking SSRIs versus 811 depressed patients taking placebo, Dr Healy determined that there were 52 suicidal acts by patients on SSRI versus 18 in the placebo group. In a pool of 638 anxious patients taking SSRIs versus 562 anxious patients taking a placebo, there were 10 suicidal acts in the SSRI group versus 1 in the placebo group. When these data sets were combined, in the 1569 patients on SSRIs there were 62 episodes of suicidality versus only 19 episodes in 1373 patients on a placebo. This analysis clearly shows that SSRIs can cause some children who were not depressed to begin with to become suicidal. Dr Healy believes the FDA should do more about the industry's practice of paying medical professionals to publish fraudulent research papers ghostwritten by PR firms. "While it is not FDA's brief to regulate the academic literature," he states, "the possibilities of a close to fraudulent representation of data and of extensive ghostwriting does set up an argument that these apparently scientific articles are in fact infomercials rather than the real thing." "If these articles are essentially advertisements," Dr Healy says, "it is much less clear that FDA can throw their hands up and plead an inability to do anything about the production of such materials." Former Federal fraud investigator, Allen Jones, will also be testifying at the hearing and he too has testified before about the over-promotion and marketing of psychiatric drugs. "The pervasive manipulation of clinical trials, the non-reporting of negative trials and the cover-up of debilitating and deadly side effects," Mr Jones says, "makes it impossible to prescribe, or take, these drugs with any level of meaningful informed consent." "Doctors and patients alike," he states, "have been betrayed by the governmental entities and officials who are supposed to protect them." During an investigation in Pennsylvania, Mr Jones learned all about Big Pharma's methods promoting the sale of psychiatric drugs by corrupting public officials and says, "conflicts of interest permeate the testing, approval and marketing of drugs in America." "Academic researchers with industry ties," he explains, "put favorable spin on dubious clinical trial results and then the embellished results are presented to FDA Advisory Boards peopled with Pharma consultants, grantees and advisors." "These results," he reports, "are further embellished in medical journals by still more academics on drug company payrolls." From there, he says, this body of misleading research becomes institutionalized by "expert panels" in treatment guidelines generated by additional academics and researchers with financial ties to the industry. As a fraud investigator, he discovered a hidden account in Pennsylvania where drug companies were funneling money to the state employees who were in charge of deciding which psychiatric drugs could be included in the treatment guidelines for the official list of drugs covered by public health plans like Medicaid and prescribed to people in all state institutions and programs. According to Mr Jones, the employees "were given unrestricted educational grants that were deposited into an off-the-books account, unregistered, unmonitored, literally operated out of a drawer." Mr Jones also found that the drug makers were paying these same state employees honorariums of up to $2,000 to speak at industry events and giving them perks such as lavish meals and trips. After the SSRIs and atypical antipsychotics were successfully added to the state formulary list, Mr Jones reports, Pennsylvania spent a combined total of $139 million in 2003, for those 2 classes of drugs alone. Last month, the former Pennsylvania Chief Pharmacist, identified as being on the take by Mr Jones during his investigation, was indicted on felony and misdemeanor conflicts of interest charges involving accepting money from drug companies while a state employee with great influence over the drugs that would added to the state formularies to be prescribed to patients in Pennsylvania. "I predict we will be seeing many more prosecutions of this type," Mr Jones says, "as the extent of drug company corruption of government officials becomes known." Another prominent SSRI expert making a return visit to testify once again is Dr Joe Glenmullen, a psychiatrist and clinical instructor in psychiatry at Harvard Medical School, and the author of the book, "Prozac Backlash," which describes his experiences of watching patients become suicidal while taking SSRIs. He has testified previously about a specific side effect of SSRIs called akathisia, that he and many other experts say, can make some patients so agitated that they feel death would be a welcome relief. "This side effect is so well established," Dr Glenmullen told a previous panel, "that it is clearly described with SSRIs in the Diagnostic and Statistical Manual, the DSM, the American Psychiatric Association's official diagnostic manual." "If you look at the transcript of the FDA hearing on this very side effect 10 years ago," he stated, "you will see the FDA saying repeatedly we don't know what to do, we need more research." "It is a tragedy," he added, "to be here 10 years later and hear the FDA saying the same thing." "The industry's response to this side effect," he continued, "has been to blame the underlying psychiatric conditions of patients, to dismiss legitimate medical case reports as anecdotes, and to scare the media away from the subject, claiming that it would frighten patients away from treatment." "Well, I prescribe SSRIs and I warn patients," he told the panel, "and they are not frightened away from treatment." In conclusion, Dr Glenmullen clearly stated that the suicidality in SSRI patients was not caused by an underlying psychiatric condition, that it was caused by akathisia. "Let's stop blaming the victims," he said, "and deal with this very real side effect." www.opednews.com/articles/genera_evelyn_p_061205_ssri_experts_head_to.htm | |
Posted by siddy, 13:57 12 December 2006Linda,
I can't exactly say that I felt I lambasted you just made my point of view known. My main issue is my experiences are different than yours and as I said before I have nothing against people sharing their experiences or worries but ultimately it is peoples personal choice whether they take drugs. I have nothing against the promotion of information but I feel it has to be done in an balanced way. I can probably dredge up websites siting the benefits of antidepressants but ultimately I don't promote their use I just say that I feel they help me and if people are on their lowest ebb it might help them. My experience of drugs is also affected by the fact I have been working in Psychiatric care for 15 years and have met hundreds of people on many differing anti-psychotic and anti-depressive medication. I decided on the basis of how it affected the people I worked with it was a reasonably safe risk. I am concerned when people have an axe to grind, in the grand scale of things this issue is irrelevant so I won't be continuing this debate | |
Posted by Linda, 14:53 12 December 2006Thanks for coming here and sharing your views, Siddy. If you want to share experiences of people you've worked with, and indeed if you want to find info that says the drugs are beneficial, then that's fine. None of the info I've put on here has been challenged by anyone. A good discussion would probably make what I've said sound more convincing, LOL, but I can see you've got other things to do and that's fine too.
I wish I could share with you everything I've absorbed about psychotropic drugs. There's so much. I don't know how taking them can be a matter of personal choice when most people, including physicians and psychiatrists, are uninformed about them. For example, when I took them myself, my views were similar to most everyone else's here -- not keen to take them, but felt it was necessary. Vague warnings about side effects, possible self-harm, etc -- well, I accepted there could be a risk, but felt just as you said -- that it's a risk to an extent to take any drug, and I really needed to get well. I learned about this idea that my serotonin must be low, which my doctor espoused, and felt sure that boosting it must help. I unknowingly made some mistakes simply because I didn't have a clue what was really going on. For a start, there's debate about the whole process of diagnosing people, and mental illness in general. There's undeniable evidence that pharmaceuticals have had a big hand in pathologising "conditions" so that they can sell drugs. Depression, for example, used to be viewed decades ago as a largely self-treatable condition, and there weren't many drugs targeted at it. And manic depression was an extreme case. It should strike anyone as odd that these diagnoses have proliferated so much in past decades. It did seem odd to me, before I educated myself about any of this. For example, "bipolar" was somehow the flavour of the week in the psychiatric world, and why? OK, so your "diagnosis" might be dubious, or it might be drugs you're already on that are worsening your condition, etc. The usual next step is to be prescribed a drug that "targets" your diagnosed condition. Over 80% of people who present depressive symptoms at their doctor's, walk away with a prescription for antidepressants. The belief -- not a proven fact, but a belief -- is that depression is caused by low serotonin. You take a drug that increases serotonin. Or maybe that isn't it, maybe boosting norepinephrine and dopamine will help instead, so you get bupropion. Again, it struck me early on as odd that doctors could be so sure these conditions were caused by deficiencies in these neurotransmitters. And if they were so sure, why did they take such a hit-and-miss approach? If depression is a low-serotonin issue, why use bupropion? My own shrink thought Effexor would be "better" because it targeted 2 neurotransmitters, not just one. My doctor was equally enthusiastic about Cymbalta. Effexor wasn't "better" for me at all. The same simplistic idea is applied to schizophrenia. Must be too much dopamine, so suppress it with Zyprexa or somesuch. (Actually, the way this happened was that through trials of the drug, drug companies got some favourable if dubious results, and then told doctors that the underlying condition must be one of dopamine overabundance, since their drug "helped".) These people are then chemically subdued and have to suffer the side effects that come with tinkering with neurotransmitters in a way that nature never would. That's the next point: side effects. What we hope when we go on ADs is that we'll be one of the lucky ones who don't get any. Again, most people don't think where those side effects come from. They come from artifically boosting serotonin, which throws things out of whack in all sorts of ways, all over the body. Most of your serotonin is actually in your digestive tract, not in your brain. What's more, too much serotonin has degenerative effects that aren't always easy to spot until people have been on the drugs for years. One thing that all of these drugs do is to mess about with blood sugar. You may gain weight on the drugs. Or at some point in the future you may find you can't shift the weight when you want to. You can develop more serious symptoms like Parkonsonism, or crippling fibromyalgia. How many people would still take these drugs if they knew the full spectrum of risks, and that they would be making some permanent changes in the structure of their brains? I wouldn't have touched them. There's evidence for all these things, plus a hundred other "side effects." Some of them do not appear until the drug is discontinued. I would list again, here, the problems I am still having 7 months down the line after discontinuing mine, but I'd rather not lay myself open to the victimisation-line again just now. There's no scientific evidence that any lack, or overabundance, of any neurotransmitter is responsible for any psychiatric condition. You, Siddy, or anyone else, are more than welcome to try to find some. So, the question here is: How can anyone make what you say is a personal, informed choice to take the drugs when: Their diagnosis may be wrong They are told by doctors that the condition is caused by neurotransmitter problems They are told by doctors that psychotropic drugs will treat the condition They are not aware of the full spectrum of risks that the drugs entail I say again: I never would have touched them if I had known. What I want to do is disseminate this information so that other people are more informed before they make what may be for them a very big mistake. I'd just like to address, as well, this idea of personal choice. That it's OK for people to address their condition in whatever way "works," even if it's drugs. First, there's enough info here and elsewhere to show that taking the drugs is about as enlightened a move as having a lobotomy, and I hope this is seen by the mainstream to be the case while I am still alive. Secondly, I think a distinction needs to be made bewteen coping strategies, and strategies that address the roots of the problem -- what helps, and what actually works. Coping strategies for depression are in abundance here on this forum, and they do help a lot of people. They include things like exercising, getting sunlight or doing light therapy, taking various herbs or over-the-counter remedies, taking a holiday, pampering yourself, and then taking drugs when these things fail. Psychotropic drugs don't cure anything. Some people feel they make things more manageable. Maybe the drugs even help lift the condition for a while. But the rate of relapse is high. The long-term problem remains. If people want to do these things then yes it's their choice. But what they need to understand is that the underlying problem needs to be treated successfully for it to go away permanently, and none of these strategies are likely to do that in and of themselves, though they may make life easier. It's understandable why people don't realise this as a rule. Modern Western medicine treats conditions by trying to alleviate the symptoms, usually with drugs. Clogged arteries and high cholesterol? Lower the "bad" cholesterol then. High blood pressure? Take a drug to lower it. These approaches do not address the reasons why these conditions presented in the first place. The associated drugs do not remove the problem, and they cause side effects. The standard approach to depression is no different. Develop strategies to cope. You can take drugs if you want. That doesn't stop the depression from coming and going, possibly all your life. The approaches I've been discussing on this forum are ones that get at the roots of the problem. In essence they are changing diet and supplementing, to address a lack of nutrition causing biochemical imbalances that can result in a myriad of physical and mental problems; and therapy, whether it be self-help or with a therapist, to address maladaptive thought patterns that perpetuate the depression. If you are aware of others, Siddy, I'd love to hear about them. Also, I'm aware that most people think I'm too extreme about the diet/nutrition approach, that people are generally aware of what they need to eat to be healthy, and that they can get all the nutrition they need from a reasonably balanced diet. I used to think this too. It is wrong. I can give more evidence on this too, if anyone wants it, though I guess it would have to go in a different category on the forum. Any thoughts on anything I've said here, please feel free to respond. Linda. | |
Posted by Linda, 18:22 14 December 2006 | |
Posted by Linda, 18:25 14 December 2006Against Biologic Psychiatry
by David Kaiser, M.D. Psychiatric Times December 1996 Vol. XIII Issue 12 ---------------------------------------------------------------------------- ---- As a practicing psychiatrist, I have watched with growing dismay and outrage the rise and triumph of the hegemony known as biologic psychiatry. Within the general field of modern psychiatry, biologism now completely dominates the discourse on the causes and treatment of mental illness, and in my view this has been a catastrophe with far-reaching effects on individual patients and the cultural psyche at large. It has occurred to me with forcible irony that psychiatry has quite literally lost its mind, and along with it the minds of the patients they are presumably supposed to care for. Even a cursory glance at any major psychiatric journal is enough to convince me that the field has gone far down the road into a kind of delusion, whose main tenets consist of a particularly pernicious biologic determinism and a pseudo-scientific understanding of human nature and mental illness. The purpose of this piece is not to attempt a full critique or history of this occurrence, but to merely present some of the glaring problems of this movement, as I believe significant harm is being done to patients under the guise of modern psychiatric treatment. I am a psychiatrist trained in the late 1980s and early 1990s, and I use both psychotherapy and medications in my approach to patients. I state these facts to make it clear that this is not an antipsychiatry tract, and I am speaking from within the field of psychiatry, although I find it increasingly impossible to identify with this profession, for reasons which will become clear below. Biologic psychiatrists as a whole are unapologetic in their view that they have found the road to the truth, namely that mental illnesses for the most part are genetic in origin and should be treated with biologic manipulations, i.e., psychoactive medications, electroconvulsive treatment (which has made an astounding comeback), and in some cases psychosurgery. Although they admit a role for environmental and social factors, these are usually relegated to a secondary status. Their unquestioning confidence in their biologic paradigms of mental illness is truly staggering. In my opinion, this modern version of the ideology of biologic/genetic determinism is a powerful force that demands a response. And when I use the word ideology here, I mean it in it's most pernicious form, i.e., as a discourse and practice of power whose true motivations and sources are hidden to the public and even to the practitioners themselves, and which causes real harm to the patients at the receiving end. Biologic psychiatry as it exists today is a dogma that urgently needs to be unmasked. One of the surest signs that dogmatists are at work here is that they rarely question or attempt to problemitize their basic assumptions. In fact, they seem blissfully unaware that there is a problem here. They act in seeming unawareness that they are caught up in larger historical and cultural forces that underwrite their entire "scientific" edifice. These forces include the medicalization of all public discourse on how to live our lives, a growing cultural denial of psychic pain as inherent in living as human beings, the well-known American mixture of ahistoricism and belief in limitless scientific progress, and the growing power of the pharmaceutical and managed care industries. These self-proclaimed visionaries, oblivious to all of this, boast of real scientific progress over what they consider to be the dogma of psychoanalysis, which had up until recently reigned as psychiatry's premier paradigm. Now, it is not my intention to defend psychoanalysis, which had its own unfortunate excesses, although I do use psychoanalytic principles in the kind of psychotherapy I do. However, it is quite clear to me that the grandiose claims of biologic psychiatry are wildly overstated, unproved and essentially self-serving. Biologic psychiatry has had its successes, particularly with recent antidepressants like Prozac and newer antipsychotic medications such as Clozaril. Medications can effectively improve depression, relieve severe anxiety, stabilize serious mood swings and lessen psychotic symptoms. These successes are real in that they improve the quality of life of patients who are genuinely suffering. But in reality, i.e., the reality of treating patients, medications have profound limitations. I know that if the only tool I had in treatment was a prescription pad, I would be a poor psychiatrist. The center of treatment will always need to be listening to and speaking with the patients coming to me. This means listening seriously to what they say about their lives and history as a whole, not merely listening for which symptoms might respond to medications. Although it seems astounding that I would have to state this, biologic psychiatrists as a whole really only listen to that portion of the patient's discourse that corresponds to their biologic paradigms of mental illness. It is the nature of dogma that its practitioners hear only what they want to hear. So what are the limitations of biologic psychiatry? First of all, medications lessen symptoms, they do not treat mental illness per se. This distinction is crucial. Symptoms by definition are the surface presentation of a deeper process. This is self-evident. However, there has been a vast and largely unacknowledged effort on the part of modern (i.e., biologic) psychiatry to equate symptoms with mental illness. For example the "illness" major depression is defined by its set of specific symptoms. The underlying "cause" is presumed to be a biologic/genetic disturbance, even though this has never been proven in the case of depression. The errors in logic here are clear. A set of symptoms is given a name such as "major depression," which defines it as an "illness," which is then "treated" with a medication, despite the fact that the underlying cause of the symptoms remains completely unknown and essentially untreated. I have seen repeatedly that, for example, in the case of depression, once medications lessen the symptoms, I am still sitting across from a suffering patient who wants to talk about his unhappiness. This process of equating symptoms with illnesses has been repeated with every diagnostic category, culminating in perhaps one of the greatest sophistries psychiatry has pulled off in its illustrious history of sophistries, namely the creation of the Diagnostic and Statistical Manual (currently in its fourth incarnation under the name DSM-IV), the bible of modern psychiatry. In it are listed all known "mental disorders," defined individually by their respective symptom lists. Thus mental illnesses are equated with symptoms. The surface is all there is. The perverse beauty of this scheme is that if you take away a patient's symptoms, the disorder is gone. For those who do serious work with patients, this manual is useless, because for me it is simply irrelevant what name you give to a particular set of symptoms. It is an absolute myth created by modern psychiatry that these "disorders" actually exist as discrete entities that have a cause and treatment. This is essentially a pseudo-scientific enterprise that grew out of modern psychiatry's desire to emulate modern medical science, despite the very real possibility that psychic pain, because of its existential nature, may always elude the capture of modern medical discourse and practice. Despite its obvious limitations, the DSM-IV has become the basis for psychiatric training and research. Its proponents claim it is a purely phenomenological document stripped of judgments and prejudices about the causes of mental illness. What in fact it has done is the defining and shaping of a vast industry of research designed to validate the existing diagnostic categories and to find ways to lessen symptoms, which basically has meant biologic research. Virtually all of the major psychiatric journals are now about this, and as such I find them useless to help me deal with real patients. Patients are suffering from far more than symptoms. Symptoms are the signs and clues to direct us to the real issues. If you take away the symptoms too quickly with medications or suggestion, you lose the opportunity to help a patient in a more profound way. As an aside, modern psychiatrists, because they have forgotten or dismissed the real power of transference, vastly underestimate the extent to which symptom reduction is caused by mere suggestion. Not that patients should be left to suffer needlessly from what are often crippling symptoms. Relief from symptoms is a part of treatment. Modern psychiatry would have us believe that this is all treatment should be. Meaning, desire, loss and death are no longer the province of the psychiatrist. In this process patients are reduced to something less than fully human, as they become an abstract collection of symptoms without meaning to be "managed" by technicians called psychiatrists. This is in the service of medical progress and enlightened scientific thought. The biologic psychiatrist will not make the mistake of imposing their value systems on patients like in the bad old psychoanalytic days. This is, of course, a sham. Modern psychiatry now foists on patients the view that their deepest and most private ills are now medical problems to be managed by physician-psychiatrists who will take away their symptoms and return them to "normal functioning." This is more than a bit malignant. One of the dominant discourses that runs through the DSM-IV and modern psychiatry in general is the equating of mental health with "normal" functioning and adaptation. There is a barely concealed strain of a specific form of Utopianism here which blithely announces that our psychic ills are primarily biologic and can be removed from our lives without difficulty, leaving us better adapted and more productive. What is left completely out, of course, are any notions that our psychic ills are a reflection of cultural pathology. In fact, this new biologic psychiatry can only exist to the extent it can deny not only the truths of psychoanalysis, but also the truths of any serious cultural criticism. It is then no surprise that this psychiatry thrives in this country presently, where such denials are rampant and deeply embedded. I am constantly amazed by how many patients who come to see me believe or want to believe that their difficulties are biologic and can be relieved by a pill. This is despite the fact that modern psychiatry has yet to convincingly prove the genetic/biologic cause of any single mental illness. However, this does not stop psychiatry from making essentially unproven claims that depression, bipolar illness, anxiety disorders, alcoholism and a host of other disorders are in fact primarily biologic and probably genetic in origin, and that it is only a matter of time until all this is proven. This kind of faith in science and progress is staggering, not to mention naive and perhaps delusional. As in any dogma, there is no perspective within biologic psychiatry that can effectively question its own motives, basic beliefs and potential blind spots. And thus, as in any dogma, there is no way for the field to curb its own excesses, or to see how it might be acting out certain specific cultural fantasies and wishes. The rise and fall of biologic determinism in a culture likely has complicated and interesting causes, which are beyond the scope of this paper. A few comments will have to suffice. This is a culture increasingly obsessed with medical science and medical health as a sign of virtue. It is not surprising that our psychic ills would be pulled into this dominant medical discourse, essentially medicalizing our specific forms of psychic pain. It seems to me that modern psychiatry, in step with a culture which created it, assumes any suffering to be unequivocally bad, an impediment to the "good life" of progress, productivity and progress. It is now almost heresy in psychiatry to say that perhaps suffering can teach us something, deepen our experience, or point us to different possibilities. Now, if you are depressed or anxious, it has no real meaning, because as a biologic illness similar to say diabetes, it is separate from the world of meaning and merely is. Now any thoughtful person knows that something as fundamental as depression has meanings such as loss, facing mortality, unlived desires, lack of power or control, etc., and that these meanings will continue to exist even if Prozac makes us feel better. There is much more to life than feeling better or living without pain, and only a superficial and pathologic culture would need to deny this. Yet conclusions such as "depression is a chemical imbalance" are created out of nothing more than semantics and the wishful thinking of scientist/psychiatrists and a public who will believe anything now that has the stamp of approval of medical science. It seems to me that modern psychiatry is acting out a cultural fantasy having to do with the wish for an omniscient authority who, armed with modern science, will magically take away the suffering and pain inherent in existing as human beings, and that rather than refusing this projection (which psychoanalysts were better able to do), modern psychiatry has embraced the role wholeheartedly, reveling in its new-found power and cultural legitimacy. I would be remiss if I left out the obvious economic factors in psychiatry's movement toward the biologic. Pharmaceutical corporations now contribute heavily to psychiatric research and are increasingly present and a part of psychiatric academic conferences. There has been little resistance in the field to this, with the exception of occasional token protest, despite its obvious corrosive and corrupting effects. It is as if psychiatry, long marginalized by science and the rest of medicine because of its "soft" quality, is now rejoicing in its new found legitimacy, and thus does not have the will to resist its own degradation. The fact that drug companies embrace and fund this new psychiatry is cause enough for alarm. Equally telling is a similar embrace by the managed care industry, which obviously likes its quick-fix approach and simplistic approach to complicated clinical problems. When I talk to a managed care representative about the care of one of my patients, they invariably want to know what medications I am using and little else, and there is often an implication that I am not medicating aggressively enough. There is now a growing cottage industry within psychiatry in advocating ways to work with managed care, despite the obvious fact that managed care has little interest in quality care and realistic treatment approaches to real patients. This financial pressure by managed care contributes added pressure for psychiatry to go down a biologic road and to avoid more realistic treatment approaches. What this means in real terms is that psychotherapy is left out. There has thus been a triple partnership created between this new psychiatry, drug companies and managed care, each part supporting and reinforcing the other in the pursuit of profits and legitimacy. What this means to the patients caught in this squeeze is that they are increasingly overmedicated, denied access to psychotherapy and diagnosed with fictitious disorders, leaving them probably worse off in the long run. It is quite depressing to listen to the discourse of modern psychiatry. In fact, it has become embarrassing to me. One gets the strong impression that patients have become abstractions, black boxes of biologic symptoms, disconnected from the narratives of their current and past lives. This pseudo-scientific discourse is shot through with insecurity and pretension, creating the illusion of objectivity, an inevitable march of progress beyond the hopeless subjectivity of psychoanalysis. Psychotherapy is dismissed and relegated to nonmedical therapists. I actually have no objections to real science in the field, if, for example, it can help me make better medication decisions or develop newer and better medications. But in general biologic psychiatry has not delivered on its grandiose and utopian claims, as today's collection of medications are woefully inadequate to address the complicated clinical issues that come before me every day. This is all not terribly surprising given what I have outlined in this piece. There will be no substitute for the difficult work of engaging with patients at the level of their lived experience, of helping patients piece together meaning and understanding in the place of their pain, fragmentation and confusion. Patients these days are not suffering from "biologic illnesses." What I generally see is patients suffering from current or past violence, traumatic loss, loss of power or control over their lives and the effects of cultural fragmentation, isolation and impoverishment that are specific to this culture at this time. How this manifests in any individual is absolutely specific; therefore, one should resist any attempt to generalize or classify, as science forces us to do. Once you go down the route of generalization, you have ceased listening to the patient and the richness of their lived experience. Unfortunately what I also see these days are the casualties of this new biologic psychiatry, as patients often come to me with many years of past treatment. Patients having been diagnosed with "chemical imbalances" despite the fact that no test exists to support such a claim, and that there is no real conception of what a correct chemical balance would look like. Patients with years of medication trials which have done nothing except reify in them an identity as a chronic patient with a bad brain. This identification as a biologically-impaired patient is one of the most destructive effects of biologic psychiatry. Modern psychiatrists seem unaware of what psychoanalysts know well, namely how powerful are the words that a patient hears from an authority figure like a psychiatrist. The opportunity here for suggestion, coercion and manipulation are quite real. Patients are often looking to psychiatrists for answers and definitions as they struggle with questions such as who am I or what is happening to me. Of course we all struggle with these questions, and the human condition is such that there are no definitive answers, and anyone who comes along claiming they have answers is essentially a fraud. Biologic psychiatry promises easy answers to a public hungry for them. To give a patient nothing but a diagnosis and a pill demonstrates arrogance, laziness and bad faith on the part of the psychiatrist. Any psychiatrist needs to be continually aware of the very real possibility that they are or can easily become agents of social control and coercion. The way to resist this is to refuse to take on the role assigned through cultural fantasy, namely the role of omniscient dispenser of magical potions. As a whole modern biologic psychiatry has enacted this role with particular vigor and enthusiasm. At the level of individual patients this means a growing number of overdiagnosed, overmedicated and disarticulated people less able to define and control their own identities and lives. At the level of our culture this has meant an impoverishment of the discourse around such questions as what is wrong with us, as "scientific" answers replace more potentially fruitful and truthful psychological and cultural questioning. If psychiatry is to regain any semblance of legitimacy and integrity, it must strip itself of false and hubristic scientific claims and humbly submit itself to the urgent task of listening to individual patients with patience and intelligence. Only then can we have any real sense of what to say back to them. The sole philosophic basis for this new psychiatry is the championing of empiricism above all other measures of truth. Something is valid only if it can be demonstrated through experimental method, otherwise it is disregarded or relegated to "subjective" experience, which is presumed to be inferior. Now, of course, this dominance of empiricism is not limited to psychiatry, and one can easily trace the invasion of the experimental method of the "hard" sciences into the "soft" or social sciences. On a larger cultural level this can be detected in the public's infatuation with "studies," statistics and so on. This hegemony of empiricism over other ways of thinking and knowing represents an unprecedented modern achievement which has thoroughly infiltrated the cultural psyche, to the point now where the average person believes easily the claims of the biologic psychiatrist. Now as is clear from my views already expressed, a social science dominated by empiricism is a vulgar science, and there is a vast tradition in philosophy from Plato to Nietzsche which in my view irrefutably demonstrates this. However this is well beyond the scope of this piece. Suffice it to say that modern psychiatrists, like all "scientists" these days, have no time for the basic philosophic questions that have engaged the most brilliant minds of the past. Who needs questions about virtue when there is important data to collect? These biologic psychiatrists never think to ask themselves whether their own precious methods are perhaps standing on very shaky ground, say their own disavowed prejudices about what constitutes the good life. Empiricism is one way of knowing, but certainly not the only or best way. Biologic psychiatrists often use the standards of empiricism to answer their critics, in effect saying that their claims are scientifically "proven" and thus unassailable, clearly a tautological argument. I would further add that in my view many of the claims of biologic psychiatry do not even hold up to their own standards of empirical science, for example their claims about the biologic and genetic basis of many mental illnesses. In my view, the methods of experimental science are inappropriate and misplaced when it comes to understanding the complexity of the human psyche, as they can only objectify the mind and remove subjectivity from the heart of human experience, thus creating an abstract entity in place of a human mind. It is no wonder that psychiatry declared the 1980s the decade of the brain instead of the decade of the mind. In their pursuit of the human brain they have quite literally lost their minds. One way to unmask the dogma that is biologic psychiatry is to ask the question what kind of human being is being posited as desirable, "normal," or not disordered. Judging by the DSM-IV, it would be a person not depressed or anxious, without perversions or sexual "dysfunction," in touch with "reality," not alienated from society, adapted to their work, not prone to excessive feeling states and generally productive in their life pursuits. This is, of course, the bourgeois ideal of modern culture. We will all fit in, produce and consume and be happy about it. Anyone who dissents by choice or nature slips into the realm of the disordered or pathologic, is then located as such by medical science and is then subject to social management and control. Now, psychiatry has always provided this social function, as admirably shown by Foucault and others. I would submit, however, that modern psychiatry, under the guise of medical and "scientific" authority and legitimacy, has surpassed all past attempts by psychiatry to identify and control dissent and individual difference. It has done this by infiltrating the cultural psyche, a psyche already vulnerable to any kind of medical discourse, to the point where it is a generally accepted cultural notion now that, say, depression is an illness caused by a chemical imbalance. Now when a person becomes depressed, for example, they are less able to read it or interpret it as a sign that there may be a problem in their life that needs to be looked at or addressed. They are less able to question their life choices, or question for example the institutions that surround them. They are less able to fashion their own personal or cultural critique which could potentially lead them to more fruitful directions. Instead they identify themselves as ill and submit to the correction of a psychiatrist, who promises to take away the depression so they can get back to their lives as they are. In short, the very meanings of unhappiness are being redefined as illness. In my view this is a dismaying cultural catastrophe. I do not mean to suggest that psychiatry is solely to blame for this, given how wide a cultural shift this is. However, I do think that psychiatry has not only not resisted its role here, but actually has fulfilled it with considerable hubris. Thus in my view the whole phenomenon of biologic psychiatry is itself a symptom or acting out of a larger, underlying cultural process. Unhappiness and suffering are not seen as resulting from real cultural conditions; for example, the collapse of traditional institutions and the ever increasing hegemony of rampant consumerism in American culture. Nor is suffering seen in the context of what it means to exist as a human being in any historical period. Historical and existential discourse about unhappiness is increasingly supplanted by medical discourse, and biologic psychiatry has served as one of the major mouthpieces for this kind of pseudo-scientific and frankly pathetic medical discourse about what ails us. I am increasingly astonished about how unable the average patient is now to articulate reasons for their unhappiness, and how readily they will accept a "medical" diagnosis and solution if given one by a narrow-minded psychiatrist. This is a cultural pathologic dependence on medical authority. Granted, there are patients who do fight this kind of definition and continue to search for better explanations for themselves which are less infantilizing, but in my experience this is not common. There is a frightening choking off of the possibility for dissent and creative questioning here, a silencing of very basic questions such as "what is this pain?" or "what is my purpose?" Modern psychiatry has unconscionably participated in this pathology for its own gain and power. It is a moral, not scientific issue at stake here, and in my view this is why many astute Americans rightfully distrust this new psychiatry and its Utopian claims about happiness through medical progress. So what kind of psychiatry am I advocating here? First of all, I think it is unclear whether the field can extricate itself from its current infatuation with technology and its own power to use it. When one reads psychiatric journals now, one senses a dangerous giddiness about the field's "discoveries" and "progress," which in my view are wildly and irresponsibly overstated. All the momentum, which is mainly economically driven, is pushing psychiatry toward further biologism. Having said this, what I am advocating is a psychiatry which devotes itself humbly to the task of listening to patients in a way that other medical practitioners cannot. This means paying close attention to a patient's current and past narrative without attempting to control, manipulate or define it. From this position a psychiatrist can then assist the patient in raising relevant questions about their lives and pain. The temptation to provide answers or false solutions should be absolutely avoided here. Medications are used judiciously for lowering painful symptoms, with considerable attention paid to the psychological effects of medication treatment. Diagnosis should play a secondary and small role here, given that little is known about what these diagnoses actually mean. Above all suggestion, coercion, normalization and control need to be assiduously guarded against, as these are natural temptations that arise out of the dynamics of power that exist between psychiatrist and patient. A more humane psychiatry, if it is even possible in today's cultural climate, must recognize the powerful potential of the uses and abuses of power if it is not to become a tool of social control and normalization. As I have outlined in this piece, these abuses of power are by no means always obvious and self-evident, and their recognition requires rigorous thought and self-examination. The psychiatrist plays a particular role in cultural and individual fantasies, and an intelligent psychiatrist must be aware of the complexity of these fantasies if he is to act in a position outside these projections and fantasies. This requires real moral awareness on the part of a psychiatrist who wishes to act intelligently. What I am advocating for in outline form as stated previously are the minimal requirements necessary for the field of psychiatry to reverse its current degradation. What is essential at this time is for psychiatrists and other clinicians to speak out against the ideology known as biologic psychiatry. Dr. Kaiser is in private practice in Chicago, and is affiliated with Northwestern University Hospital | |
Posted by Linda, 20:27 20 December 2006If you want to stay away from, or discontinue, psychotropic drugs, here is the Withdrawal and Recovery link:
http://health.groups.yahoo.com/group/Withdrawal_and_Recovery/ If you truly want to be medication-free, and well, and are willing to do what it takes to accomplish this, then you are welcome. You need to be prepared to be honest with yourself, to look at your life and make changes to your thought patterns and also to address fundamental needs that are possibly not being met. You also need to be prepared to change how you eat, to use nutritional supplements, and to do a slow taper off your medication -- 10% or less at a time. If you're in doubt about any of this, please think hard before you join. You might want to dip into the info on the many links in this topic. You're also welcome to contact me if you have any questions. It is possible to lead a healthy, drug-free life. There is hope. Linda. | |
Posted by Jeff, 08:19 21 December 2006The first thing I want to ask is how did you get these text exerpts from some of these publications? Last time I tried, I still couldn't copy and past from a .pdf image file...
I just read this entire thread in the past two hours (excluding most of the info found through the links.. that would take weeks), and I am momentarily at a loss for words. I have, in the last two years, come more and more to be disgusted and outraged with the "mental health" sytem here, the pharmaceutical industry, and society's views on all of this. Often times I am appalled by this issue or that, not looking at it in terms of the larger picture. I have done so much research lately on so many issues, but you have done at least as much research on this set of issues alone as I have done on every thing else put together. Thank you so much for posting all of this. I have come lately to view a healthy life more in terms of a vaiety of different facets... One cannot address the issues surrounding psychotropic medications without considering nutirtion. One can not address mental illness without considering this or that, and so on... And the more I look at my life wholistically, and take better care of myself, the more things just seem to come together. In the past year, I have discontinued 3 psychotopics which I have no doubt were doing so much more harm than good. Now I am working on tapering off of the one that I have been on for 10 years (max dose, I might add), and I find myslef wondering if the long term taking of this chemical may have had permanant or protracted consequences. It seems almost a no brainer to me that it has. All of this leaves me concerned about the illness... A lot of the material you have posted implies that there is no illness, but of course I assume that these people are talking in generalizations. "magically take away the suffering and pain inherent in existing as human beings" There is an excerpt of what I am talking about. Clearly there are MI people who have a disorder. Schizophenia for example, or catotonic depression, cannot be written off as "the suffering and pain inherent in existing as human beings", and the suffering and deaths of these people just be accepted as such, nor can every such case be explained by this or that chemical exposure or nutriotional deficiency, for these conditions were present in some capacity long before humanity developed it's tendencies of depriving itself of nutrients or exposing itself to toxins. There is a biologic basis for some cases of some of these conditions, and as such, a "medical" explanation and treatment should be sought. The problem is that psychiatry, corporations, and government have together all gone too far with this, and in any case, a wholistic approach has never been emphasized in modern science here. Continuing with my concern about the illness... speaking particularly about my illness... I had an unreasonable and unacceptable presentation of "psychiatric" problems for many years before I ever started an psychotropic meds. In fact, it amazes me all the time that I ever even survived to the point where I started taking meds, and amazes me even more that I have survived since, considering I got worse after starting meds. Having said all that, I don't know how much my remaining med helps me, but looking at how I was before it is not a pretty picture. I can only hope that my more wholistic approach now will pull me through. I just wanted to add something which I have frequently thought lately about these forums. These are the only forums I have ever found where there appears to be some significant portion of the people focusing on facts and solutions, instead of whining, self pity, and especially ignorance which are usually most of what I find on forums for mental health, or mental illness if you will. Anyway, I am very glad to have found these forums. And now for another cup of organic Earl Grey... | |
Posted by Linda, 08:44 21 December 2006Hi Jeff,
Yes I read some of your other posts here, and thought it sounded like we were of a similar mind in many ways. I'm American too BTW, though I've been living in England for 12 years. I grew up in Missouri. When I came to this forum I met some kind-hearted and sympathetic people. There's lots of good advice here about coping with symptoms. But I was severely depressed for months on end, desperate for help, and unfortunately there was no help to be had anywhere. "Coping" with symptoms isn't enough when you're as deep in the pit as I was. Suicide started to seem like the only way out. I remember thinking exactly the same thing you said just now: "What I feel goes beyond the pain of having a 'down period' in life. This is excruciating, every minute of the day, and I can't take it anymore." So even the people like Dr. Moncrieff, who talk perfect sense about psychotropic drugs being harmful and not offering much help, didn't light any hope in me. When I wrote to Dr. Moncrieff about this, her only suggestion to me was, "Have you tried exercise?" which I thought was rather patronising. What gets left out of a lot of this is nutrition. Don't underestimate its power to hurt or harm, Jeff. And if you have taken/are taking psychotropic drugs, this is especially true. If you look into studies that have been done on aboriginal societies, like hunter-gatherers, you will find that diseases like schizophrenia and cancer are rare or non-existant. What you do find is that when these societies switch over to a Western-style diet, that's when they start getting ill. Diabetes was unknown in the Pacific before World War Two. Once these island societies adopted the American diet, cases of type 2 diabetes soared. It is now as high as 50% in some places. I could give many more examples like this. Nutritional deficiencies can show themselves in myriad ways before they reach the deprivation levels in related diseases like scurvy, pellagra, pernicious anemia, etc. Doctors mostly don't recognise this because they don't look. They are trained to spot and treat symptoms. This is what Western medicine does. By beginning to look at your mind and body holistically, looking at the nutrition you are giving them and how you are taking care of them in general, you are starting to break out of this "treating symptoms" mode of thinking, and reaching out to something deeper and more profound. If this piques your interest, a good starting point might be Linus Pauling's book "How to Live Longer and Feel Better" (which can be got from Amazon.com.) He was a pioneer of something called orthomolecular medicine, though there are other big names to look into there as well (the Shute brothers, Abram Hoffer). Pauling won a Nobel Prize for his work on vitamin C megadosing, which was ironically largely ignored and written off as nonsense. Anyone who follows his advice will find that it does actually work, as long as you take the vitamin in the amounts that he tells you to (which is perfectly safe). I have headed off 4 or 5 colds now in a matter of a day or two each, by megadosing the way he recommends. You might also like to have a look at this site: http://www.orthomolecular.org/ I'll just add here that I, like many others on the Withdrawal and Recovery list, would not have got out of the hole I was stuck in without altering my diet and starting to take supplements. Now I'm getting better, day by day, and I see my life stretching before me again -- better than I ever thought possible. I hope this helps Jeff. Let me know if you've got further questions, and happy hunting -- there's enough info on the links here to keep a person busy for days. Linda. | |
Posted by Linda, 09:04 21 December 2006A couple more links to good nutritional sites:
http://www.mercola.com/index.htm http://www.westonaprice.org/splash_2.htm You might also want to have a closer look at the article I posted here by Dr. David Kaiser, regarding biological psychiatry. Conditions like "schizophrenia" (which is actually a nebulous cluster of symptoms) are real. Depression is real. The mistake is in attibuting their causes to some faulty biological mechanism, which then lends itself to "fixing" with medication. If the problem is a medical one, e.g. thyroid, then a medical doctor needs to treat that. If the problem is a nutritional deficiency, then that needs to be treated at the source. A deficiency in a trace mineral like selenium can cause depression; trace mineral deficiencies are very common in the Western world now, where intensive farming has sucked the nutrients out of the ground, and fertilisers have not replaced them (fertilisers only replace about 4 of the many trace elements that are depleted by farming). What doctor would be able to tell you that you need selenium? More likely, you will be told that you have a serotonin deficiency and will be given an antidepressant. Again, hope this helps Jeff, Linda. | |
Posted by Linda, 07:39 26 January 2007The following exerpt talks about the reasons why people are prescribed, and take, psychiatric drugs. It's important to keep in mind that there's no awareness here of the potential for nutritional deficiencies, food allergies, etc, to cause mental illness; but there is a lot of wisdom here nonetheless.
Introduction: What Is Your Ultimate Resource? from Your Drug May Be Your Problem: How and Why to Stop Taking Psychiatric Medications, by Peter Breggin M.D. & David Cohen Ph.D. This book is filled with technical and scientific information about psychiatric drugs (especially their dangers) and how to withdraw from them. However, it is also important to understand the underlying psychological, social, and ethical principles that may affect your decision to use or not use psychiatric drugs. We can learn a great deal about ourselves and how we view life by asking, "Where do we turn when we feel emotionally upset or despairing? Where do we go when life seems unendurable and we have little or no hope left? What are our ultimate resources in life -- the places and persons to whom we turn for help, direction, and inspiration?" Our Final Resort All people seem to need faith, but the varieties of faith seem infinite. For many individuals, the ultimate resort or resource is religious or spiritual: God and prayer, or other beliefs and practises, and perhaps a trusted minister, priest, rabbi, or counselor. For others, the ultimate resource may be a loved one -- a husband or wife, a parent, a friend. Still others may believe that they themselves are the ultimate resource. They may turn to creative work, nature, pets, hobbies, sports, or some other seemingly individual or personal persuit. Increasingly, people nowadays also turn to science to find answers about how to live life. Probably for most people, the final resort is a combination of these resources: God, nature, science, other people, and oneself. Ultimately, all human resources are related. Commitment to a loving, zestful, rational, principled life becomes the cornerstone of life and the final resource. Resort to Drugs Many people, however, rely on another, more limited resource when they face psychological or social crises. They turn to psychoactive or mind-altering substances. Although they may believe or hope that they are relying on seemingly objective science, in reality they are placing their faith in drug company marketing -- and so are their doctors. Consider the seemingly different situation with respect to recreational or illicit drugs. For untold millions throughout the world, the last resort is alcohol, tobacco, or substances such as marijuana and cocaine. Many turn to them when they feel on the verge of experiencing painful emotions. In the extreme, they become addicted to these substances and build their lives around them. When they eventually try to give up their addiction, they may discover that they have no other resources left and nowhere else to turn. Their lives have been emptied by their reliance on drugs. They must rebuild from scratch their faith in God or other ethical convictions, their trust in other people, and their reliance on themselves and their love of creative work or nature. Seeking Relief If people do feel better when drinking alcohol or smoking marijuana, it is because they feel better when their brain is impaired. Psychiatric drugs are no different. The people who take such drugs may feel less of their emotional suffering. They may even reach a state of relative anesthesia. But to the degree that they feel better, it is because they are experiencing intoxication with the drugs. Most of us can empathise with people who are willing to sacrifice brain function in return for a blunting of emotional suffering, but should therapists or doctors offer this alternative? Should we ourselves turn to this alternative in our own lives? Is the cost too great in terms of brain dysfunction and the failure to deal with the real issues in our lives? The resort to psychoactive substances, whether legal or illegal, recreational or psychiatric, involves a compulsive narrowing of focus in the search for solutions to life's problems. Almost always the emphasis is on obtaining relief from painful emotions, too often regardless of the potential cost. What Suffering Tells Us Emotional suffering is inevitable in life. But it has meaning -- a purpose. Suffering is a signal that life matters. Specifically, it is usually a signal that something in our lives that matters a great deal needs to be addressed. Depression, guilt, anxiety, shame, chronic anger, emotional numbing -- all of these reactions signal that something is amiss and requires special attention. The depth of suffering is a sign of the soul's desire for a better, more creative, more principled life. For example, when faced with a patient in deep depression, should we immediately focus on relief of the pain? On the contrary, we should respond by saying that the pain is a signal of the intensity of the person's spirit: "The strength and intensity of your suffering indicates the strength and intensity of your spirit. Your discomfort shows how alive you are. Now imagine if you could learn to turn all that self-destructive energy into creative energy and a love of life." The degree to which we suffer indicates the degree to which we are alive. When we take drugs to ease our suffering, we stifle our psychological and spiritual life. Instead, we need to find a way to untangle that twisted energy and to redirect it more creatively. Sometimes this process of personal and psychological growth can be helped by insightful psychotherapy or other therapeutic and educational techniques -- including those that facilitate our understanding of early childhood sources of the suffering. At other times, the process is helped by our understanding of the problems in our immediate lives, such as an unhappy marriage, a frustrating job, or a difficult financial situation. Sometimes this understanding involves learning new principles of living with which to guide ourselves more effectively, which, in turn, may entail a recommitment or a new commitment to spiritual or philosophical ideas, and especially love for ourselves, for other people, and for life or some other guiding ideal. Sometimes it involves a therapist who cares so much about the client that the client can begin to care about himself or herself. The New Ultimate Resource The last ten to twenty years have seen a drastic change in viewpoint regarding the ultimate resource of moral and psychological guidance: Regardless of their religion or philosophy, many educated and informed people have come to believe that psychiatry and psychiatric drugs provide the best last resort for themselves when in psychological distress. Indeed, such drugs are increasingly the first resort. It appears that we have replaced reliance on God, other people, and ourselves with reliance on medical doctors and psychiatric drugs. The ultimate source of guidance and inspiration is no longer life itself with its infinite resources but biopsychiatry with its narrow view of human nature. This view of ourselves is a most astonishing one. It suggests that most if not all of our psychological, emotional, and spiritual problems are “psychiatric disorders” best treated by specialists who prescribe psychoactive drugs. Our emotional and spiritual problems are not only seen as psychiatric disorders, they are declared to be biological and genetic in origin. The propaganda for this remarkable perspective is financed by drug companies and spread by the media, by organised psychiatry and individual doctors, by “consumer” lobbies, and even by government agencies such as the National Institute of Mental Health (NIMH). As a result, many educated Americans take for granted that “science” and “research” have shown that emotional upsets or “behaviour problems” have biological and genetic causes and require psychiatric drugs. Indeed, they believe they are “informed” about scientific research. Few if any people realise that they are being subjected to one of the most successful public relations campaigns in history. These days, your doctor is likely to suggest medication for relatively mild degrees of emotional upset or distress; even a few weeks of moderate sadness or anxiety are apt to lead to a prescription. If your child has been difficult to deal with for a few weeks at home or in school, that, too, is likely to bring out the prescription pad. The probem may have lasted for only a short period, but the drug treatment may go on for years or even for a lifetime. Psychiatric diagnosis has become so widespread that it is almost impossible to mention any kind of “feeling” to a medical doctor without being assigned a psychiatric label and prescribed the latest psychiatric drug. And this scenario is not limited to strong emotions or serious distress. Feeling fatigued? take Prozac. Feeling as though you’ve lost your enthusiasm or direction? Take Paxil or Zoloft, especially if Prozac hasn’t worked. Feeling trapped in an abusive relationship? Take Effexor, Luvox, or lithium. Feeling a little nervous? Take Xanax, Klonopin, or Ativan. Having trouble disciplining your child? Give the child Ritalin, or Dexedrine, or Adderall. Having trouble focusing on work that bores you? Try Ritalin for yourself. Having ups and downs of any kind? Take any number of psychiatric drugs. What Do We Really Know About How Our Brains Work? Do we know what we are doing to our brains and minds when we take psychiatric drugs? Do we know what we are doing to our children when we give them these substances? Consider this extraordinary reality. The human brain has more individual cells (neurons) than there are stars in the sky. Billions! And each neuron may have 10,000 or more connections (synapses) to other brain cells, creating a network with trillions of interconnections. In fact, the brain is considered to be the most complex organ in the entire universe. With its billions of neurons and trillions of synapses, it is more complex than the entire physical universe of planets, stars and galaxies. Scientists have well-developed ideas about how the physical universe works. They possess mathematical formulae for describing the various forces that control the relationships among physical entities from black holes to subatomic particles. All these forces also affect the human brain. However, the living processes of the brain add complexities unknown in the physical universe. Those trillions of interconnections between brain cells, for example, are mediated by hundreds of chemical messengers (neurotransmitters), as well as by hormones, proteins, tiny ions such as sodium and potassium, and other substances. We have limited knowledge about how a few of these chemical messengers work but little or no idea as to how they combine to produce brain function. The Science Behind Psychiatric Drugs The public is told that a great deal of science is involved in the prescription of psychiatric drugs, but this is not so – given that we know so little about how the brain works. The knowledge that we do have about the effects of psychiatric drugs on the brain is largely limited to test-tube studies of biochemical reactions utilising ground-up pieces of animal brain. We simply do not understand the overall impact of drugs on the brain. Nor do we have a clear idea about the relationship between brain function and mental phenomena such as “moods” or “emotions” like depression or anxiety. We don’t even know where to begin looking because we don’t fully understand how the brain functions. Some theoreticians would urge us to focus on the molecular level by looking for biochemical imbalances. But that’s sheer speculation. Why would a biochemical imbalance be at the root of feeling very depressed any more than it would be at the root of feeling very happy? And if there were biochemical substrates for extreme sadness and extreme happiness, would that fact make them diseases? The idea of individual biochemical imbalances is wholly at odds with the complexity of the brain. Besides, whose biochemical imbalance are we looking for? That of the child who is out of control or the caregiver who has difficulty disciplining? That of the child who isn’t learning or the teacher who hasn’t figured out how to reach this child? That of the individual who becomes anxious in dealing with people or the adult who abused the individual as a child? That of the person who is deeply depressed over a lost loved one or the doctor who recommends electroshock? That of the person who feels insecure or anxious or the doctor who thinks that the person’s problems require drugs? In short, whose brain isn’t working right? Are There Biochemical Imbalances? As one of our colleagues recently said, “Biochemical imbalances are the only diseases spread by word of mouth.” Individually, we must all use our own intuitive understanding of life to determine the likelihood that our problems are caused by some as-yet-undetected brain dysfunction rather than by conflicts in the home, at work, or in society, painful life experiences, confused values, a lack of direction, or other aspects of human life. Of course, our bodies can affect our emotional outlook. We all find it much easier to maintain a bright and enthusiastic attitude when physically healthy than when physically ill. And anything from lack of sleep to the common cold can affect our moods. However, doctors commonly give people psychiatric drugs without checking for obvious signs of serious physical disorder, such as hypothyroidism, estrogen deficiency, or head injury from a car accident. Moreover, they seem particularly prone to overlooking the importance of physical symptoms in women. Some women with obvious signs of a hormonal disorder or heart condition are put on antidepressants and antianxiety drugs without first being required by their internists or psychiatrists to undergo a physical evaluation. It is therefore theoretically possible that some anxious or depressed people may be afflicted with an as-yet-undetected physical dysfunction. But this speculation doesn’t justify the unfounded conclusion that people in emotional distress are beset by specific biochemical imbalances or that such imbalances can be corrected with drugs. In our own experience, most people with depression and anxiety have obvious reasons for how they feel. These reasons are often apparent in their everyday lives and may be complicated by past experiences in childhood or earlier adult life. But even if some people do turn out to have subtle, undetected biochemical imbalances, there is no reason to give them drugs like Prozac or Xanax that cause biochemical imbalances and disrupt brain function. Let us again consider the final resort. Is it defined by our values, our family and friends, and ourselves – or by a medical doctor with a prescription pad? What Do We really Know About Psychiatric Drugs and the Brain? Almost all psychiatric drug research is done on the normal brains of animals, usually rats. As noted earlier, much of this research involves grinding up brain tissues to investigate the gross effects of a drug on one or more limited biochemical reactions in the brain. More sophisticated research involves micro-instrumentation that injects small amounts of drugs into the living brain and measures the firing of brain cells. Yet even these more refined methods are gross compared to the actual molecular activity in the brain. For example, we have no techniques for measuring the actual levels of neurotransmitters in the synapses between the cells. Thus all the talk about biochemical imbalances is pure guesswork. More important, what’s actually being studied is the disruption of normal processes by the intrusion of foreign substances. This research in no way bolsters the idea that psychiatric drugs correct imbalances. Rather, it shows that psychiatric drugs create imbalances. In modern psychiatric treatment, we take the single most complicated known creation in the universe – the human brain – and pour drugs into it in the hope of “improving” its function when in reality we are disrupting its function. The notion that Prozac corrects biochemical imbalances is sheer speculation – propaganda from the biological psychiatric industry. But disruption of biochemical reactions in the brain, causing severe biochemical imbalances and abnormal rates of firing among brain cells, is a proven fact about Prozac that cannot honestly be disputed by anyone who knows the research. How does the brain react to the intrusion of psychiatric drugs such as Prozac, Ritalin, or Xanax? The brain reacts as if it is being invaded by toxic substances; it tries to overcome, or compensate for, the harmful drug effects. In the process, the brain literally destroys its own capacity to respond to the drug. It numbs itself to the drug and, in so doing, actually kills some of its own functions. So when a doctor tells us that Prozac is putting our biochemistry into balance, we are being badly misled. In actuality, Prozac is profoundly disrupting the function of the brain. Prozac, Ritalin, and Xanax, like most psychiatric drugs, overstimulate particular neurotransmitter systems either by increasing the output of a neurotransmitter or by preventing its removal from the synapses between nerve cells. Prozac, for example, overstimulates a chamical messenger called serotonin by blocking its removal from the synapse. The brain reacts by initially shutting down the release of serotonin and then by reducing the number of receptors that can respond to the serotonin. These self-destructive processes in the brain are relatively easy to research. They were demonstrated in the private laboratories of Eli Lilly – the manufacturer of Prozac – even before the drug was approved for marketing by the Food and Drug Administration (FDA). Long before the marketing of Prozac, the drug was known to routinely cause drastic biochemical imbalances rather than to correct them. How long does it take the brain to recover from the imbalances caused by Prozac? We don’t have an answer to this critical question. Why not? Because drug companies and the scientific community have never carried out the relatively simple and inexpensive research that would be required. Yet we should suspect that the brain does not always recover from Prozac or similar antidepressants such as Paxil and Zoloft. We already know that the brain’s recovery from exposure to many psychiatric drugs can be prolonged and that full recovery may never take place. Studies have demonstrated this outcome for stimulant drugs such as the amphetamines, including Dexedrine and Adderall, that are prescribed for children. Although the final verdict concerning Ritalin isn’t in, its similarity to other stimulants is such that we should be concerned about its capacity to cause irreversible changes. We also know that irreversible changes can occur in response to the drugs used to treat schizophrenia, such as Haldol, Prolixin, and Risperdal. These drugs can cause permanent, severe impairments of brain function. Indeed, we should suspect that any psychoactive drug – any drug that affects mental function – tends to produce irreversible changes in some if not most people. What hope can we have that bathing the brain in a psychiatric drug will actually improve the overall function of this mysterious organ? Almost none. In fact, as already noted, most of what we know about the various neurotransmitters has been gathered by studying how psychiatric drugs disrupt or spoil their functioning. What if We Treated Our Computers the Way We Treat the Brain? Imagine what would happen if we treated our much simpler computers in the same way as we treat the brain in psychiatry. Consider the case of a computer that is “crashing” too often. With considerable poetic license, we can compare this mechanical dysfunction to the human tendency to become “overwhelmed” or “overloaded” with depression, anxiety, or obsessions and compulsions, and unable to function easily in everyday life. Perhaps the computer is crashing for reasons having to do with its hardware. For example, the computer may need more memory or a new hard drive. Alternatively, the problem may be traceable to its software – to one or more of the programs installed on the computer. Then again, the operator of the computer and its programs may be responsible. Or the source of the problem could lie outside of the computer and even outside the office, as in the case of power surges. When troubleshooting such a problem, computer experts routinely take all of these factors into consideration – the computer, the program, the operator, and the power source. If the cause of the problem isn’t immediately apparent, they may run experimental tests or programs in order to diagnose the problem. The approach taken by psychiatrists and other medical doctors, by contrast, is both simple-minded and destructive. In contemporary psychiatry, the doctor almost always assumes that the problem lies in the “hardware” of the brain (i.e., “biochemical imbalances”). In the words of one well-known psychiatrist, emotional and behavioural difficulties are caused by a “broken brain.” Modern psychiatrists seem to consider themselves brain consultants, but they have little knowledge with which to establish that expertise. Unlike computer consultants, psychiatrists have no way of identifying or locating the source of the problem in a patient’s brain. So the patient must take their “expert” assertions on faith. How would you react if your computer consultant treated your computer the way psychiatrists treat patients and their brains? Suppose your consultant invariably concluded that the problem must lie in the hardware of your machine rather than in the program, the operator, or some external factor such as the power source. Suppose your consultant always began by pouring toxic agents into your computer. Further suppose that your consultant never guaranteed you a good result while continuing to pour toxic agents into your machine without regard for the consequences – and, when pressed for an explanation, made vague references to “crossed wires” or “electrical imbalances” in your computer but never looked inside, conducted any tests, or provided a definitive physical diagnosis. How long would you put up with such nonsense from your computer consultant? Not very long. If computer consultants behaved like psychiatrists, we would fire them. Yet, tens of millions of people put up with even more slipshod, irrational treatments involving their far more complex and vulnerable brains and minds. What This Viewpoint Does to Us What happens when we start viewing a human being as an object? We lose our own capacity for rationality and for love. It is impossible to reduce a person’s emotional suffering to biochemical aberrations without doing something psychologically and morally destructive to that person. We reduce the reality of that individual’s life to a narrowly focused speculation about brain chemistry. In taking such a distorted view of the person, doctors also do harm to themselves. They suppress their natural tendency to be empathic toward other human beings. Thus, in their efforts to be “objective” and “scientific,” biological psychiatrists and doctors end up doing very destructive things to people, including themselves. Herbal and “Natural” Remedies Although this book is about psychiatric medications that are approved by the FDA, many readers may have questions about psychoactive herbal remedies that can be obtained over the counter (OTC). They may wonder if these more “natural” substances can be used instead of psychiatric drugs during the withdrawal process or as a general substitute. In brief, we do not recommend the use of psychoactive herbs for these purposes. Many people believe that such natural remedies are likely to be safer than prescription drugs. This is the implication conveyed by many books that evaluate herbal medicines, such as PDR for Herbal Medicines (1998) and Alternative Medicine (1994). Both list far fewer adverse effects for typical herbal remedies (such as St. John’s Wort as an antidepressant or ginseng as a stimulant) than are usually described in the literature for psychiatric drugs used for corresponding purposes (such as Prozac or Ritalin). Nonetheless, anyone who uses psychoactive herbs should do so with caution. Some of these herbs have recognised adverse effects. For example, ginseng, in large doses, can cause dependence with serious adverse effects. The scientific citations typically listed for herbs are mainly non-English language reports not readily accessible to the ordinary reader in the United States. The composition of many of these substances, including St. John’s Wort and ginseng, is very complex, with numerous active agents that have been little studied. Preparations from different manufacturers – or even from the same manufacturer – may not be standardised. And, finally, even though the FDA often fails to live up to its mandate, FDA-approved drugs are usually more thoroughly studied than herbal remedies in regard to adverse effects. Some people might believe that a long history of use without known ill effects is in itself a good indication of a psychoactive herb’s safety. However, consider two of the most widely used natural psychoactive substances, alcohol and tobacco. Both were once recommended by physicians for medicinal purposes, and both have been heavily promoted by government and corporate interests. Alcohol has been used for many reasons by untold millions of human beings since before recorded history, but only in the last few decades have the harmful effects of chronic excessive alcohol use been generally recognised. Society has also become increasingly aware of the association between acute alcohol use and many forms of violence and accidents. Likewise, tobacco has an ancient history of ritual use in Native American societies and, in more recent centuries, of widespread chronic use in Western society. But the dangerousness of smoking did not gain widespread recognition until a few decades ago. Any drug that affects the mind and brain should be viewed with caution, especially in the context of daily or persistent use. And any person who decides to use herbal remedies should read as much as possible about them. To use these agents is, to some extent, to step into the unknown. By contrast, all psychiatric drugs have well-documented, serious hazards. Even if psychoactive substances were harmless, we would question their use for “therapeutic” or “psychiatric” purposes – that is, to overcome psychological and social problems. The use of a psychoactive substance for such purposes is wrong in principle because it represents an attempt to fix the brain instead of the problems that lie within the person’s internal life, relationships, and environment. It is understandable, of course, that people want relief from emotional suffering, just as they tend to take aspirin, ibuprofen, or other drugs for head, muscle and joint pains. The latter treatments play a valuable role, especially if they are administered over the short term. However, both aspirin and ibuprofin also have many potentially serious adverse effects, ranging from stomach ulcers to stroke. The use of “emotional pain-killers” is more questionable. If a person gets headaches because of the stress of a conflicted marriage or a frustrating workplace, it would ultimately be self-defeating to rely on pills instead of dealing with the issues involved. Besides, all psychiatric drugs have far more negative effects on brain and mind function than do aspirin or ibuprofin. Psychiatric medications are, first and foremost, psychoactive or psychotropic drugs: They influence the way a person feels, thinks, and acts. Like cocaine and heroin, they change the emotional response capacity of the brain. If used to solve emotional problems, they end up shoving those problems under the rug of drug intoxication while creating additional drug-induced problems. There is another lesson to be gained from how long it has taken us to recognise the dangers of tobacco and alcohol. Because it has taken centuries to grasp the damaging effects of these natural substances on individuals, families and society, we cannot blithely assume that we can learn about the dangers of psychiatric drugs in a matter of months or years. Many drugs are effective in bringing about the short-term relief of emotional suffering. Alcohol, for example, affects the same general neurotransmitter system as tranquilisers like Xanax, Valium, Klonopin, and Ativan. It has similar clinical effects, too. Millions of people “take a drink” to relax or calm down, to relieve anxiety or even depression, and to fall asleep more easily. Yet alcohol, much like the tranquilisers, has many negative effects on behaviour, tends to worsen the very problems it is used to treat, and can become addictive. The question, then, is not “Do drugs affect mental processes?” Many drugs are called “psychoactive” precisely because they have effects on the mind. Rather, the question is, “Should they be prescribed as treatments?” This book is aimed at helping people understand some of the medical and psychological dangers of relying on psychiatric drugs, but it can only hint at the psychological and social void created by such reliance on mind-altering agents. The book also offers appraoches to coming off psychiatric drugs, but, in this context too, it can only hint at the kinds of resources to which people must turn to live a meaningful and satisfying life. The choice is not between psychiatric drugs and some other “therapy” but between psychiatric drugs and all the resources that life can offer us. | |
Posted by Jeff, 08:12 26 January 2007Thanks, Linda. That was interesting (what I read of it). I didn't read it all, because I have been really out of it, lethargic, sleepy, and apathetic for the past week. When I get like that, I can not remember anything that I read, and cannot concentrate, so I don't waste my time or effort on it.
I hope I improve in these regards very soon, because I am taking two very demanding and challenging classes this semester, which require about 20 hours a week of studying outside of class. Needless to say, I haven't studied a bit in the last week, because I have been preoccupied with using all of my mental effort and will just to keep my eyes open. This week has been no different from any other January in the past X number of years. But I have only had a few weeks like this this winter, spaced out, and I keep coming back out of it enough to function. Ordinarily, I would just be a zombie for 6 months straight from Dec through May. So I guess that's a start. A couple days ago, I was esentially turned down for an experimental treatment on the grounds that I am "not depressed enough". After the call, I believe I just thought about killing myself some more and then went back to sleep, LOL. Not depressed enough? HAHAHAHA!!!!!!! | |
Posted by Linda, 10:15 26 January 2007I'm sorry to hear you're feeling so poorly Jeff. I believe you posted on Withdrawal and Recovery, and I responded. Have you read the files that were sent to you, and have you looked into changing your diet and starting supplements? These things will help a lot with how you are feeling right now.
Let me know if I can help :) Linda. | |
Posted by Jeff, 19:17 26 January 2007I have actually not read much of anything on Withdrawal and Recovery.
However, I have been tapering extremely slowly off of my last remaining psychotropic (I am on a 1 year plan to taper off of it), and I have already been using supplements for months, to replace those substances that may be in short supply in the food I eat, and also to add more of certain things which are recommended for depressive types or people with hormonal problems. My supplements include: Protein powder - containing all of the essential amino acids, plus numerous other non-essentials Anti oxidant multiplex Cal-Mag Chromium B-complex Iron Extra pantothenic acid (a B vitamin) Extra Vitamin C from time to time St John's Wort Ashwaghanda Macca "Free form" amino acid - Tyrosine. I am very doubtful that the website would recommend anything which sounds good & that I am not already using. This belief of mine helps support and justify my apathy in regards to reading any of it. | |
Posted by Linda, 21:24 26 January 2007OK Jeff, that's certainly your choice. If you decide you do want help, you can post this supplement info, plus dietary info, on the site, and Catherine will advise you. There is a specific healing protocol that people follow there in order to do what they do.
Best wishes for a successful taper of your drug and for future healing, Linda. | |
Posted by Jeff, 21:39 26 January 2007I have lately been reevaluating my eating habits, and it has occured to me recently that I consume far too mcuh sugar from the dried figs that I eat, and I have a slice of pumpkin bread a few days a week. Each slice of this probably has an ounce of refined sugar and at least 2 or 3 ounces of white flour. As much as I believe that getting only about 10% of my calories from the aforementioned food sources shouldn't be harmful, especially considering that most of the sugar is from a natural source, I am hopeful that it actually is harmful. I've decided to stop eating figs and pumpkin bread and see what happens.
I am repeatedly confronted with the unfortunate reality that food is not for enjoyment at all, it is for nutrition. Every food that I enjoy is something that needs to be absolutely forbidden from my diet. I regularly go back to one food item or another (such as figs, or before that it was dates) thinking that this half-a**ed excuse for a snack food, which I enjoy not nearly as much as what I would like to eat, can't be that bad for me, considering that it is natural. No matter how many times I prove myself wrong on that point, I have not yet learned to be obsessive enough about nutrition to stay on a strict enough diet. I am hoping that the little bit of enjoyment food I have been having has been the culprit, because I found this to be very true when I went through the same thing with the dates. Figs are far lower in sugar than dates, and I don't eat much of the pumpkin bread, so I thought it would be ok. But I am hoping that I was terribly wrong again. | |
Posted by Linda, 07:59 27 January 2007Jeff, the culprit is overall diet and nutritional supplements. You pay more attention to these things than most people, but what you are doing is not quite what your body needs -- this is why you are feeling the way you do.
I suggest you try following the healing protocols from Withdrawal and Recovery; and if you are still having problems, do a one-off consultation with Catherine, who will tailor your programme to your individual needs. You will have trouble coming off your med if you are feeling as bad as you are now. Like I said, it's completely up to you. However, though cutting figs out of what you eat might help a little, it isn't going to make a huge impact on your mood. What's more, when you are sure about what you need to cut out of your diet, it ceases to have a pull on you and over time you don't miss it. I will always love the taste of chocolate, cake, ice cream, all that stuff. But I'm happy not to eat it because I like how I'm feeling without it, and I know what it does to me when I eat it. I hope this helps Jeff. Change takes courage. Sometimes I think our bodies make us feel so bad to give us a nudge in that direction. Best, Linda. | |
Posted by Joannet, 16:45 6 February 2007Can I just say a big thank you to you Linda.
I found this forum yesterday and have been reading through bits and pieces as I get the time and brain power. I havent read all on this section yet but have found it really interesting and am sitting here having a rethink about my life style and my depression. I was prescribed Seroxat in my ealry 20s and out of desperation took them. However I didnt feel right and didnt take them for very long. I just suddenly stopped, which was not the best thing to do but I did and went through hell. My mum was so angry when she knew what I had been prescribed and taken, even the nurse on the NHS Direct phone line was shocked when I rang and asked for help! Sorry I digress from what I wanted to say. Basically I am going to go home and read this section again and read the nutrition section again and make some changes. I accept there is no over night "cure" this will take time but time is what I have. I just wanted you to know that all the hard work you have done posting all this information has touched some one and they are going to make some changes. | |
Posted by Linda, 20:19 6 February 2007I'm pleased to help anyone I can. I'm glad you've found the info here useful Joannet.
I came off my own antidepressant cold turkey 9 months ago. I was actually given the basic info I needed, but was so keen to be drug-free that I ddn't really pay attention, and ended up in difficulties for a long time. Sounds like you've been there too. In fact Seroxat is notorious for causing withdrawal problems. It must have taken some determination for you to be able to get off it. Please let me know if I can give you any further assistance; there's a lot in these topics to read. Good supplements are particularly important for someone who has taken psychotropic drugs, even if it was some time in the past. Best wishes, Linda. | |
Posted by Anonymous, 00:10 8 February 2007I found this excerpt from http://www.mercola.com/2004/jul/14/vitamin_d_book.htm
4. You mention that bright light therapy is effective for treating depression and SAD. Is this for the vitamin D, or is another component/result of the UVB rays responsible for the benefit? I ask because studies have found that low vitamin D may contribute to chronic fatigue and depression (1,2) and another study found that vitamin D was more effective in treating depression than using light boxes. Do you agree with these findings? Bright light therapy is effective in treating seasonal affective disorder because of its effect on suppressing melatonin production in the pineal gland. However, often people during the winter suffer from malaise, muscle weakness, muscle aches and bone pain that often can exacerbate their depression. A study has been conducted demonstrating that vitamin D supplementation during the winter does help reverse some of the symptoms associated with SAD. Has anyone ever tried vitamin D??? I was thinking of giving it a go. The pills are pretty cheap in Boots. I want to stay away from St Johns Wort because of the whole messing with the pill thing. (Not that I am even remotely interested in that.....I hate cuddles at the mo!) Jen x Its a shame you can buy sertatonin in a bottle! (well, that isn't labelled as Prozac of citlopram (sp) | |
Posted by Jeff, 03:12 8 February 2007Between regular exposure to sunlight,a nd consumption of producst with significant amounts of vitamin D, and other thing(s) necessary for making and processing Vit D in the body, I imagine that I am already getting well more Vit D than required, soi I have never tried adding it as a supplement, that I can recall.
Vitamin D deficiencies are really pretty rare in advanced nations, unless the individual has an unusually restrictive diet and is not supplementing. That isn't to say that extra vit D may not be good. Maybe it works wonders to have extra, I have no idea. | |
Posted by Linda, 08:21 8 February 2007Hi Jennifer,
I'm glad you're finding some interesting info on the Mercola site. A lot of their dietary advice is sound. However, I'm not so sure about this article you mention here, an interview with the author of a book about the benefits of sunlight. In a broad sense it's good in that it connects sunlight with general health, as well as vitamin D. I'd beware some of its claims however. You said: *** studies have found that low vitamin D may contribute to chronic fatigue and depression (1,2) and another study found that vitamin D was more effective in treating depression than using light boxes. Do you agree with these findings? I'd say that chronic fatigue and depression have a myriad of causes, some of which can be nutritional deficiencies. So addressing the deficiencies would be helpful. I would be careful about looking for a magic bullet though. It's best to supplement a broad range of vitamins, plus fish oil, as well as eat a healthy diet, so that all bases are covered. Jeff said that vitamin D deficiency is rare in the western world. However, levels of vitamin D tend to be far lower in temperate and northern regions than they would have been for our ancestors living in Africa; even those who lived here, but spent a lot of their time outside. They did not shut themselves up in an office all day. Many people get the daily RDA of vitamin D, but the RDA is always the lowest amount of a substance needed to prevent the associated deprivation disease, in this case rickets. Does that mean that we all get enough vitamin D if we get the RDA? No. Here in Britain, the sunlight is only intense enough for our bodies to manufacture vitamin D during a few months out of the year. The rest of the time the body is relying on its stores. I think it is very sensible to supplement vitamin D during the other months. There are also recent studies suggesting that people get more colds in the winter versus the summer because vitamin D has a part to play in the immune response, though this needs looking into further. You quoted from the article: ***Bright light therapy is effective in treating seasonal affective disorder because of its effect on suppressing melatonin production in the pineal gland. This is sheer speculation. It is an idea which has not been proved. You asked: ***Has anyone ever tried vitamin D??? I was thinking of giving it a go. The pills are pretty cheap in Boots. Make sure it is vitamin D3 and not the synthetic D2. You said: ***Its a shame you can buy sertatonin in a bottle! (well, that isn't labelled as Prozac of citlopram (sp) I would advise you to continue to have a look at the info here in this topic. There is no scientific evidence that low serotonin is the cause of depression, or that boosting serotonin helps cure it. In fact, though boosting serotonin can give the high that some people associate with the relief they feel from depressive symptoms while on SSRIs, artificially high amounts of it damage the brain and the body. That isn't to say that a little extra serotonin, produced naturally, can't help. This is one thing sunlight is known to do. It can act as a natural antidepressant, it helps you to feel better. My idea is that this is why many people who think they have SAD feel better in the summer: the sunlight is helping them. When there's less of it in the winter, the depression comes back. BTW light boxes don't produce enough light, or the right kind, to stimulate the body to produce vitamin D. I hope this helps Jennifer. One last thought: it's worth looking at one's life to see what might be causing depression: diet, illnesses, medications, relationships, career, any needs that aren't being met. Through the influence of misguided psychiatrists, doctors, and the drug companies, people are too focused on looking for chemical solutions to depression. At best these may ameliorate some symptoms; at worst they can ruin a person's life. Kindest regards, Linda. | |
Posted by PurpleIvy, 13:51 8 February 2007I would like to add a little balance to this thread. I have info regarding antidepressants too and also professional advice received regarding medication in general. The fact is that some people regard medication as a necessary part of their treatment and are helped by it.
I have often been advised by qualified pharmacists... ie. people with a high level of training that within any group of drugs there is a variation in how YOUR body will metabolise that drug compared with the next person. Therefore if one doesn't suit you, eg. is not effective, or level of side effects is not tolerable, then it is well worth asking your health professional, whether consultant or GP, to prescribe an alternative. THis has had incredible results in my case. A change of medication (an antidepressant) has enabled me to go back to work.... I have been off 12 weeks with SAD cited as cause on Doctors Medical Certificate. I was so lethargic and feeling rough on the first medication, I feel brighter and more alert on the second and well. My libido is not back to normal, but is greatly improved, to a point where it has actually made me want to resume that area of life too. Many people regard 'pills' as being the quick fix all. Well it seems to me that the further into any sort of depression you get, the harder it is to get out, so something that will prevent you going too far 'down' may stop things getting bad to the point where it is hard to do anything about it. Think about how many millions of people use medication of thousands of diffferent types every year. Then think about the relatively small number that have a significant and lasting problem with it. None of us takes medication lightly, I don't suppose. But the fact is that the risks are probably much lower than if you endanger your own life by smoking, drinking to excess or taking part in other risky activities. I suspect that by saying this I will be criticised by some, but there are some for whom medication is an appropriate treatment and we need ot be allowed to do what is right for us. | |
Posted by Suzie, 18:12 8 February 2007A healthy diet and nutrition is common sense and should be followed to achieve good health both mentally and physically. But I all have to agree with Purplecrab. There is a place in our society for modern day drugs. What about Bipolar disorder and Schiztophrenia (bad spelling I know).. Without medication people with both of these disorders would be guaranteed to harm either themselves or another innocent person......this is a FACT!!!! Without constant medication these people would be locked away and have no quality of life whatsoever.
It is also a FACT that I was 9 stone, went to the gym and did either netball, squash, babmington and aerobics 6 days a week, ate a healthy diet and still suffered as much as I do today with depression. The only difference is when I was younger I could cope with the malaise better than I do today. Chronic illness is not cured by drugs but they enable people to lead as normal a life as possible.......something they would not be able to do without them. Why should a drepressive illness be any different. It should be a personal choice and what is best for the person involved. I too would not have been able to continue working and maintaining a normal life if I had not been given the drugs I am on now. They weren't the first drugs I tried and I have had to try three different ones before finding the right one for me. I don't like the side effects but for me the fact that I can just function normally outweighs the side effects of the drugs. | |
Posted by Linda, 19:33 8 February 2007Suzie and Purplecrab,
You're welcome to browse this topic and take from it what you will. I'm not going to go to other places on this list and tell both of you that you must not take drugs. That is your decision. And both of you, like many others, feel you are being helped by them. If you do come here and browse, though, I would urge you to read the information that is actually here. It contradicts much of what you have said about diagnoses, and the efficacy of drugs in treating these conditions. The reason why I put that information here was just that -- to inform people. If you'd like to read what's here and respond specifically to that, then maybe we can be on more level footing here. I'll take some of the basic points that have been mentioned for the moment then. You both are speaking from the point of view of people who feel they have been helped by these medications. You have been lucky to experience few side effects. You have not been taking the drugs long-term, have not been on and off them (correct me if I'm wrong) many times, or stuggled with your condition worsening despite (or because of) the meds. You do need to know that it is no exaggeration to say that there are people out there whose lives have been destroyed by these drugs, and by the doctors who were supposed to help them. To say that smoking or drinking are bigger risks to health is both misguided and frankly insulting to these people. I belong to one list for people in withdrawal from psychotropic drugs. Almost every day, someone new joins. You have not witnessed the desperation of those whose functioning has deteriorated on these drugs, who have developed long-term permanent problems, who have been put on cocktails of medications, who developed a set of symptoms with one med and were subsequently diagnosed with a new disorder and given more meds for that on top of the current ones. People who are suicidal. Who are experiencing Parkinson symptoms, uncontrollable movements of their bodies, who even feel that they are being tortured from within (a condition called tardive akathesia). Please don't tell me that you are taking more risk with drinking or smoking than you are with these drugs. Thank whatever god is up there that these things did not happen to you -- but understand that they do happen to others. I also find it disturbing to hear anyone say that people with bipolar disorder and schizophrenia are dangerous and need to be on meds, possibly for life. Read the article here on biological psychiatry. Read various points of reference here, specifically the story about the lady who was diagnosed as bipolar because of a reaction she had to a medication, and spent much of the rest of her life tweaking doses of lithium and feeling like a zombie inside. Read in the nutrition topic about how a doctor has cured schizophrenia with vitamins, and what he says about the inhuman treatment of these people at the hands of doctors dishing out medications and electroconvulsive therapy. People come to the withdrawal list who are fed up with being drugged and want their lives back. Many of them come with these very diagnoses. They change their diets, supplement, address the original problems they had where necessary, and those diagnoses are history. Any doctor who thinks that long-term drugs are appropriate ought to see what is going on at that list, and the healing that is taking place. Other people too have claimed that I am scaremongering, that even taking aspirin is dangerous. The fact of the matter is that the truth about how these medications work, and what they do to the body, is not generally known, for a variety of reasons. And also, aspirin does not change levels of neurotransmitters and alter fundamental parts of biochemistry, so that comparison is a meaningless one. Many people on Outside In have also said that they eat a healthy diet and it hasn't helped with the depression. I would ask you to visit the Nutrition topic, because what a person calls "healthy" may actually not be, for them. I used to think I ate healthily too, and knew what a healthy diet was, but I didn't. At the end of the day, I wanted this topic to be here to inform people about these drugs, but also to say that there are other ways of addressing depression. Of course it's a person's choice, but that choice needs to be an informed one. You may end up being lucky in that the serotonin boost gives you a mood boost that ameliorates some of the depressive symptoms, and you may have few or no noticeable side effects. It is your choice what to do from there. However it is important to realise that if the original cause of the depression is not addressed, it is likely to still be there when the medication is withdrawn, or to return. I do think about the millions of people taking thousands of different kinds of medication, and it saddens me deeply. Medications are handed out far too freely in Western countries. Our doctors treat symptoms, not causes. They often don't even think to look for the cause of a problem before they prescribe a drug. Of course medications can be helpful and even life-saving, but they are often just not needed. A case in point is the millions of pounds the NHS spends on statins, which are no more of an effective treatment for high cholesterol or heart disease than is a placebo. Purplecrab and Suzie, no one is questioning your right to take medications, or your choice, which is a private matter for you. I would just ask you to please read the information here and respond to that, question or challenge it, but look at what it has to say and compare that to what you think you know. There may be some surprises, some food for thought. Or maybe you will decide you disagree, or are not interested. That is OK too, but please at least recognise that psychiatric diagnoses and the DSM-IV doctors use to make them are subjective and not set in stone; also that psychiatric drugs may not do what you think they do for everyone, and that many people have been damaged by them. I wouldn't argue that symptoms associated with bipolar disorder or schizophrenia don't exist. However, by classifying them rigidly as mental illnesses and then telling people that they need drugs for this, disempowers them to continue looking for answers. There are many possible causes for these symptoms and I would firmly refute the ideas of biological psychiatry, that there are mysterious chemical imbalances, or that it's genetic. This is drug industry spin. I hope this clarifies my position a bit better. Please try some of the links I've posted here, or read some of the articles. Regards, Linda. | |
Posted by Suzie, 20:53 8 February 2007Linda
Just to clarify a few points. I have suffered with depression for 25years. I have been on a variety of drugs, a lot of which have not helped in anyway whatsoever. I have not taken the drugs constantly and have had long periods without them. I don't believe they have caused me any long term problems. I have also on many occasions tried to bring myself back from depression without medication without much success. I have no underlying reason to be depressed. My life could not be happier. I have currently been taking the drug I am on now for 6years and had I not been given the support and advice from my GP and primary health care team I truly believe I would not be here today. If I wanted to come off these AD's tomorrow (hopefully someday I will) I would have the full support of my GP. I fully appreciate your comments but it appears to me that the people who visit the recovery site you mention have indeed had bad experiences with both drugs and the people prescribing them. This is not the case for everyone and my comments address this. My GP has also become a personal friend and I trust her totally. I don't believe she would not give me the best advice available just to line the pockets of drug companies. To address your comments regarding GP's just handing out AD's without any thought. Do you really believe this when the NHS and funding is so bad.... Wouldn't it be easier and cheaper for the GP's to just tell these people to "pull themselves together" and point them in the direction of self help. Like you say, its an informed decision that evey individual has to make for themselves. | |
Posted by Linda, 21:26 8 February 2007I'm glad to hear that things are improving for you Suzie, and that you have an understanding doctor. Many doctors really want to help people and I don't believe they are deliberately trying to con us to make money for the drug companies. Their bias is just at such a deep level that they think they are helping us with the drugs. Our doctors are trained to prescribe drugs, that is their job basically, and it seems to be a rare person who breaks away from that thinking and considers other options. I doubt if many doctors would tell someone to just pull themselves together, but on the whole they are much more likely to prescribe a pill than they are to suggest something like counselling. Counselling isn't as available as it needs to be.
I'm also glad to hear that you have not noticed long-term damage from the drugs. It sounds like you're OK with how things are right now. I'd just like to say though, that even given your personal history of depression, I hope no one has suggested that depression might be part and parcel of your life, or that you might have to continue to be on and off drugs. If you're confident that there are no emotional reasons why you should be depressed, then physical issues need to be explored. When I talk about nutritional deficiencies sometimes causing depression, I don't mean those that cause someone to starve or develop severe deficiency diseases. Linus Pauling, who won the Nobel Prize for his research into vitamin C, had a mother who was in and out of psychiatric hispitals all her life, and died young and very ill. No one could ever work out what was wrong with her, until they were able to pinpoint the cause of her death: pernicious anemia, caused by a vitamin B12 deficiency. A symptom of B12 deficiency -- a symptom of most any kind of nutritional deficiency -- can be mental illness. This can occur before other more obvious physical symptoms, and doctors may never see the connection. Also, some of us need more of a certain kind of vitamin or mineral than others to achieve optimal health; it's called biochemical individuality. It follows that you would be exhibiting symptoms of deficiency even if you were getting the RDA for this vitamin every day (the RDa is the lowest amount of a vitamin needed to prevent a deficiency disease). I won't go on about this, there's more in Nutrition Info, but I wanted to say that this is an option you can explore Suzie, if you ever want to. I know what it's like to be debilitated by depression and not know how I'd drag myself through another day. To barely be able to look after my little girl. and know I couldn't work at a job if I tried. When I heard the anti-drug psychiatrists talk, I wanted to ask them what they thought I was supposed to do -- how would something like talking to a therapist help when I was in such a terrible state? How could I just think myself out of it? I felt that I was out of options, I was full of fear, and that's when I started on antidepressants. However, the key there was that it really did feel like the final option. A big reason I've stayed on this forum is because if I can, I want to offer help to people who are in similar situations to the one in which I found myself. The option I finally found, which I wanted all along and which no doctor could ever offer me, was healing through nutrition. You are welcome to look at that topic I've been maintaining on the forum. Most importantly of all, there is always hope. Mine is that even when I am no longer talking on this forum, the info I've put here will be available for anyone who is searching for answers and also feels they are about out of options. Regards, Linda. | |
Posted by Jeff, 21:52 8 February 2007I agree almost entirely with Linda's post, and I might have posted the same thing in so many words, if only I had fast typing skills and had more time, but I have neither.
However, I will point out one section of Suzie's post, which I dispute vehemantly: "....What about Bipolar disorder and Schiztophrenia (bad spelling I know).. Without medication people with both of these disorders would be guaranteed to harm either themselves or another innocent person......this is a FACT!!!! Without constant medication these people would be locked away and have no quality of life whatsoever. " Please understand that I do not say this intending offense or with any malicious agenda, but that is one of the most colossally ignorant and offensive paragraphs that I have ever read in my life. Anyone who really believes that has a great deal of mind opening and self education to embark upon after which they may reevaluate their position on such concepts, and cease to make such extreemely simple and offensive generalizations and stereotypes. Also, the positive experience that Suzie describes with the GP is a rare exception, not a rule (at least in America). I have had numerous GPs, specialist doctors, and psychiatrists, and am yet to have a remotely positive experience with any of them. Also, I do not personally know anyone at all who has ever had that kind of a positive experience with a GP, rather, almost everyone who I have ever talked with about this says the same thing that I do about them. "The medical community" and "psychiatric community" (certainly in America), is so extremely dysfunctional, backwards, and utterly broken beyond any forseeable repair, that it is almost unheard of here to have that kind of positive experience with a doctor. Lastly, I will point out that I myself, just like any diligent pursuant of self education in regards to proper holistic health, am considerably more educated with practical knowledge on issues of nutrtion and the medications that I have used than any psychiatrist or docotr who I have ever seen. The point being, a self educated consumer does not require, and in most cases has no use whatsoever for, their GP's support on their personal health choices (such as getting off of a med). They merely need the GP's prescription to have a supply of the med that they choose to take, or get off of. I truly regret that I was too ignorant, and frankly too depressed, to direct my own care in the past, and I truly sympathize with anyone who lacks the capability to do this themselves. For these people, encouragement (i.e.: ideas posted in this or the nutrition thread, or guidance from knowledgable friends or family, etc. if the individual is incabable of reading, or absorbing & retaining what they read) is crucial to get them started in the right direction. Hence, as Linda said, noone is saying people can't have their meds, nor should anyone condemn them for taking meds. Rather, people are merely attempting to encourage a more holistic and healthy perspective. | |
Posted by Linda, 22:17 8 February 2007Jeff, what you said about taking responsibility for your health is important.
In our culture, doctors have a god-like status. I was certainly raised to go to the doctor when I was ill, and I would not question what the doctor said, I would just take the medicine, and be thankful that I was helped by the expert. My American family and friends have not changed in this way of thinking. Whatever low I hit with my own depression, their way of trying to help me was to implore me to see the doctor. They simply could not see the situation any other way. To think of a doctor the way you describe, as I also do now, is unimaginable to them. My own illusions in this respect were shattered with the depression. These people were supposed to help me and all they could do was prescribe one drug after another. My doctor was of the common opinion that if you are depressed you need "more serotonin." I accepted this at first, after researching SAD and supposed serotonin deficiencies that were related. However, I did not understand where this sudden deficiency came from. I was on Effexor for a while, that didn't help, but the doctors/psychiatrists were sure it would because hey, it hits TWO neurotransmitters, and two is better than one! So . . . were they telling me I had a norepinephrine deficiency as well? No. So why did they think upping that chemical in my system was going to help? Later, my doctor was enthusing about Cymbalta, again targeting two neurotransmitters, but also it was NEW. This really started to sound fishy to me and I'd had enough by this point. It was clear to me that these meds were not well chosen by my doctor to help me individually, but rather he believed, or had been told (by drug company advertising) that whatever is newer is better. Instinct led me to learn about nutrition. Nutrition is a small part of a doctor's training and it is not hard to educate yourself beyond what most all of them know, as you say Jeff. However I am also aware that to most people, the idea of healing through nutrition sounds like just another fad or gimmick, why don't you try feng shui or yoga too while you're at it. There's so much more to it than this. I've tried to put what I've learned so far in a topic here. I also try to be a role model to people around me through what I eat, so maybe I can be a good influence on my husband and daughter if no one else. I'm not here to tell anyone what to do, what choices to make, how to run their lives. If you (whoever may be reading this) choose to come to this topic and read, however, I would ask you to read what is here and try to be open to some of the ideas. Like I've said elsewhere, there's a difference between what helps a person cope with symptoms, and what actually works to get at the roots of those symptoms. This forum is good for the former, not always for the latter, which is why there are so many people here in pain. Linda. | |
Posted by PurpleIvy, 22:51 8 February 2007Maybe we are lucky in the North Cheshire area. I live in the same county as Suzie, I don't know exactly where she lives, but know from something she said that her GP isn't the same one as mine. I'm very happy with my very supportive GP, whose main interest is having me living life normally. he doesn't hand out drugs automatically, but as appropriate. I requested a drug once in the past and was refused, because he deemed it not to be the most appropriate.
Because of the circles I move in, I know quite a few of the GPs in the area in addition to the 8 or so in my own practice. I would be happy to be in the care of any of them. And only one of these GPs is a friend. So there you are. Two people living a few miles from each other that are happy with the medical care they are receiving. Counselling has been offered to me via work and is being provided at a facility in the area too. I expect I'll be satisfied with that too. | |
Posted by Suzie, 08:16 9 February 2007There seems to be obvious difference's in the medical care that is received in my area and in the US. Counselling and CBT is always a first option at the GP surgery that I go to. We have 3 doctors who are based there, one of which will not prescribe medication unless absolutely nescessary. He too is very much into holistic and nutritional therapy.
As I have said before I have been on my medication for 6 years and had read in Norman Rosenthal's "Winter Blues" that there was a AD that was more effective for SAD than the one I am on. Armed with my book and this information I visited my doctor in September requesting that I try this drug. I was told under no circumstances would I be allowed to have this drug as the UK would not licence it for depression due to the problems that had occured in the US. One of the side effects had been that it was an appertite suppressent. Apparently people who had been prescribed the drug in the US had starved themselves to death. I was instead offered counsellling and secondary care which I am to start again in February. I consider myself to be one of the lucky ones. It saddens me to think that there are other people who are desperate for the care they need. I have taken control of my life. In the past like Linda I have gone to the doctors and taken everything he/she says as gospel and not questioned it. This is not the case now. Through literature and sites like this I can make an informed decision and if I don't like what I am being told by the "professional" then I will dispute it. Jeff, my apologies, it was not my intention to offend anybody with regards to my comments on bipolar etc. I wasn't generalising and i know it is not the case for everybody. I do know several people who would have to spend most of their life in and out of hospital if they didn't take their medication. This medication is supplemented by exercise and nutritional information but without their medication they would have dire problems and have done so in the past. This includes one person burning her house down, another continually self harming (in front of her children), another trying to kill his partner. These aren't isolated incidents for these people. I also realise that there are still areas where there are the unsavoury hospitals that in my opinion (and it is only my opinion) should never have existed. There are obviously different levels of depression and everyone finds their own way of dealing with it. At the end of the day we are all here to champion the same cause........ ideas for helping to allieviate the problem. | |
Posted by PurpleIvy, 08:19 9 February 2007Well said Suzie.
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Posted by Linda, 09:28 9 February 2007I'm pleased to hear all of this, that the standards of care are better in some places, that CBT is offered, that people can partake of this and be happy.
Again I would just ask that if anyone posts here, would you please do me the courtesy of reading some of the info here. Try some links, read some of the articles, and then discuss/debate if you like. They would challenge some of the generalisations that are being made here about mental illness and drugs and it's hard for me to discuss these things when there is no awareness on the other person's part of why I am saying some of the things I am. Like I said, I do not question the existence of symptoms of bipolar, schizophrenia, etc. However I have good reason to say that these symptoms are curable. I know people who manage the symptoms without drugs. I also know people who have cured their symptoms completely. They do not "manage," they live. This is what nutrition can do. What we put into our bodies is what our bodies build themselves from. Deficiencies and toxins can go a long way to causing ill health, but putting those right can restore it. Schizophrenic symptoms can be caused by a food allergy. Bipolar symptoms can be caused bu nutritional deficiencies. If someone is so unbalanced that they need to be tranquilised with drugs in order not to harm themselves or others, then what is needed is for them to address this; or if they can't do it themselves, for someone to help them. If this sounds crazy then let me remind you that I see people forgetting their diagnoses and healing themselves every day. I have a friend who is diagnosed bipolar, who seems half-convinced of what I say. She at least has the self-awareness to look down deep and admit that she is not sure if she wants to be "cured," because "bipolar" has become part of her identity, who she is. She is afraid that if she were no longer bipolar, she would be a different person, maybe lose her artistic abilities. I think she'd find that she would end up with a clarity and zest for life she forgot she had, and her creativity would blossom, but this is something she has to think about for herself. I just think it is disgusting that a doctor can label someone with a mental illness, and that becomes such a part of the person that they can't conceive of themselves any other way. But it does happen all too often. I think this is all I'd like to add to the discussion here for the moment. Talking about these kinds of things is important to me, but I would rather do it in regards to the information I've posted here. Linda. | |
Posted by Linda, 08:08 28 February 2007Why You Should Never Trust New Wonder Drugs, by David Healy
A drug company was last week accused of concealing evidence about the safety of the antidepressant Seroxat. According to leading psychiatrist David Healy, this is just the latest in a string of cases where patients and medical professionals have been misled about a drug's adverse effects. http://www.dailymail.co.uk/pages/live/articles/health/healthmain.html?in_article_id=434241&in_page_id=1774 | |
Posted by Linda, 11:15 25 March 2007More links
http://www.paxilprogress.org/forums/ A support site for paxil (seroxat) withdrawal. Also contains news and articles, info about protests and litigation, and info about health and supplements http://www.mindfreedom.org/ MFI is an independent nonprofit coalition defending human rights and promoting humane alternatives in mental health. http://ssristories.com/ Stories of suicide, murder, abuse, accidents, and other serious adverse effects related to use of SSRIs http://www.primalworks.com/thoughts/thought021118.html http://www.primalworks.com/thoughts/thought021125.html http://www.primalworks.com/thoughts/thought021202.html http://www.primalworks.com/thoughts/thought021209.html A series of articles written by a therapist. While his own particular approach to counselling for depression may not be everyone's cup of tea, I feel that what he says about psychotropic drugs and the ethics of using them worth pondering. http://www.guardian.co.uk/food/Story/0,2763,1687319,00.html?gusrc=rss">http://www.healyprozac.com/ This website explores threats to public safety and academic freedom surrounding the SSRI group of drugs – Prozac, Zoloft (Lustral), Paxil (Seroxat/Aropax). It makes available trial transcripts in 3 major cases involving SSRIs and suicide and homicide. It also makes available correspondence surrounding issues to do with ghost writing, efforts to draw attention to the hazards of these drugs and the dramatic changes taking place in academia as an increasing proportion of clinical research is privatised. http://www.adbusters.org/metas/psycho/prozacspotlight/lillysuicidestour/index.html "The Lily Suicides" -- info about SSRIs and suicide, and litigation http://www.paxilprogress.org/forums/ A support site for paxil (seroxat) withdrawal. Also contains news and articles, info about protests and litigation, and info about health and supplements http://www.mindfreedom.org/ MFI is an independent nonprofit coalition defending human rights and promoting humane alternatives in mental health. http://ssristories.com/ Stories of suicide, murder, abuse, accidents, and other serious adverse effects related to use of SSRIs http://www.primalworks.com/thoughts/thought021118.html http://www.primalworks.com/thoughts/thought021125.html http://www.primalworks.com/thoughts/thought021202.html http://www.primalworks.com/thoughts/thought021209.html A series of articles written by a therapist. While his own particular approach to counselling for depression may not be everyone's cup of tea, I feel that what he says about psychotropic drugs and the ethics of using them worth pondering. http://www.guardian.co.uk/food/Story/0,2763,1687319,00.html?gusrc=rss Rise in mental illness linked to unhealthy diets, say studies from The Guardian, January 16 2006 (article can be found in its entirety under Nutrition Info) | |
Posted by Linda, 11:19 25 March 2007http://www.drugawareness.org/home.html
Info about the dangers of Prozac http://www.newstarget.com/disease-mongering-engine.asp?generate=roll-me-a-new-disease Info about how big pharma sell their drugs, with a satirical disease-mongering engine that helps you market your own mental illness | |
Posted by Linda, 11:23 25 March 2007Former drug rep has horror stories to tell
By KATHY RUMLESKI, FREE PRESS REPORTER from The London Free Press Calling her book and North American tour a child-advocacy campaign, Gwen Olsen is warning parents of the dangers of some antidepressants and psychotropic drugs. After spending 15 years in the pharmaceutical industry, selling some of the drugs she now says can be deadly, Olsen has blown the whistle on her old employers and published Confessions of an Rx Drug Pusher: God's Call to Loving Arms. "I had a moral responsibility to tell people everything I knew," she said in a phone interview from her home in Texas. What Olsen knows is horrendous. Olsen's niece set herself on fire and died after being on an antidepressant. "She burned herself alive. She said . . . 'I'd rather be dead than feel crazy like I feel on those drugs.' The niece was prescribed medication following a car accident. She had problems when she stopped taking the drug. "She got addicted and when she tried to withdraw she became depressed," Olsen said. Her doctor prescribed her an antidepressant and that sent her spiralling downward, leading to suicide. Olsen was also treated for depression in 1992 with Zoloft. "I became manic psychotic. About 25 per cent of the population will have a serious adverse reaction. I was educated about these side effects and I had sold drugs that caused these side effects." Olsen walked away from her job and her career in 2000 when her bosses asked her to sell the antidepressant Celexa. In clinical studies, this medication had increased the risk of suicidal thinking and behavior in children and adolescents who had depression and other psychiatric disorders. Olsen said children are more vulnerable to the side effects of these medications because of their developing organs. "They are three times as likely to react to these drugs as an adult is." Olsen said there is "rampant economic incentive to over-prescribe drugs. "This is a social control mechanism." Psychotropic drugs were a big part of Canada's $24.8 billion pharmaceutical industry in 2005. In the U.S. $3.3 billion was spent on drugs to treat attention-deficit hyperactivity disorder. Olsen said kids diagnosed with ADHD may be helped with natural treatments. She suggested parents try getting more Omega-3 essential fatty acids, such as flax, krill or fish oil, into their children's diet and eliminate refined carbohydrates and aspartame. Olsen has another dire warning for parents. Once someone gets started on these mental-illness drugs, he or she may never get off them. "It's a lifelong customer for the pharmaceutical industry. They alter the pathology of brain chemistry so you can't get off them. They're extremely addictive." | |
Posted by Linda, 11:24 25 March 2007Love is a many-splendored...mental illness?
I want to say first and foremost that I am a romantic. I really am. I am a scientist as well, however. So, I decided to do a little research into the science of love. It is worth investigating, after all, especially on Valentine's Day. It is an emotion for sure, but what exactly makes it so powerful? It turns out Lucy Brown, a neuroscientist at Albert Einstein College of Medicine, decided to put it to the test. She found 17 people who were madly in love and scanned their brains while they were looking at a picture of their sweetheart. She wanted to find out what happens in the brain when someone experiences intense feelings of love. What she found is that there is no separate "love" part of the brain. Instead, the reward/pleasure part of the brain lights up strongly, just like it does when someone eats chocolate or when an addict gets a fix. If that doesn't take all the poetry out of love, consider this: Serotonin levels were 40 percent lower in lovebirds, just as they are in those with obsessive-compulsive disorder. So, according to Brown and her two fellow researchers, Art Aron, a psychologist at Stony Brook University in New York and anthropologist Helen Fisher, love is a motivation bordering on mental illness. And it gets worse. It is predictable that the dopamine-drenched craze that fuels intense love will wear out; sometimes over days, sometimes over years. But remember, I am a romantic. So in this one case, I will dispense with science and just follow my heart. I will buy flowers for my wife and take her out to a nice dinner. Sometimes, it is better not to know all that is going on in our brains at any given time. Posted By Dr. Sanjay Gupta, CNN Correspondent: 4:34 PM | |
Posted by Linda, 11:26 25 March 2007Serotonin and Depression: A Disconnect between the Advertisements and the Scientific Literature
Jeffrey R. Lacasse, Jonathan Leo* Jeffrey R. Lacasse is at Florida State University College of Social Work, Tallahassee, Florida, United States of America. Jonathan Leo is at Lake Erie College of Osteopathic Medicine, Bradenton, Florida, United States of America. Competing Interests: The authors declare that no competing interests exist and that they received no funding for this work. Published: November 8, 2005 DOI: 10.1371/journal.pmed.0020392 Copyright: © 2005 Lacasse and Leo. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Abbreviations: DTCA, direct-to-consumer advertising; FDA, Food and Drug Administration; SSRI, selective serotonin reuptake inhibitor Citation: Lacasse JR, Leo J (2005) Serotonin and Depression: A Disconnect between the Advertisements and the Scientific Literature. PLoS Med 2(12): e392 *To whom correspondence should be addressed. E-mail: jleo1@... In the United States, selective serotonin reuptake inhibitor (SSRI) antidepressants are advertised directly to consumers . These highly successful direct-to-consumer advertising (DTCA) campaigns have largely revolved around the claim that SSRIs correct a chemical imbalance caused by a lack of serotonin (see Tables 1 and 2). For instance, sertraline (Zoloft) was the sixth best-selling medication in the US in 2004, with over $3 billion in sales likely due, at least in part, to the widely disseminated advertising campaign starring Zoloft's miserably depressed ovoid creature. Research has demonstrated that class-wide SSRI advertising has expanded the size of the antidepressant market , and SSRIs are now among the best-selling drugs in medical practice . Table 1. Selected Quotations Regarding Serotonin and Antidepressants Table 2. Selected Consumer Advertisements from SSRIs from Print, Television, and the World Wide Web Given the multifactorial nature of depression and anxiety, and the ambiguities inherent in psychiatric diagnosis and treatment, some have questioned whether the mass provision of SSRIs is the result of an over-medicalized society. These sentiments were voiced by Lord Warner, United Kingdom Health Minister, at a recent hearing: “…I have some concerns that sometimes we do, as a society, wish to put labels on things which are just part and parcel of the human condition”. He went on to say, “Particularly in the area of depression we did ask the National Institute for Clinical Excellence to look into this particular area and their guideline on depression did advise non-pharmacological treatment for mild depression” . Sentiments such as Lord Warner's, about over-medicalization, are exactly what some pharmaceutical companies have sought to overcome with their advertising campaigns. For example, Pfizer's television advertisement for the antidepressant sertraline (Zoloft) stated that depression is a serious medical condition that may be due to a chemical imbalance, and that “Zoloft works to correct this imbalance” . Other SSRI advertising campaigns have also claimed that depression is linked with an imbalance of the neurotransmitter serotonin, and that SSRIs can correct this imbalance (see Table 2). The pertinent question is: are the claims made in SSRI advertising congruent with the scientific evidence? The Serotonin Hypothesis In 1965, Joseph Schildkraut put forth the hypothesis that depression was associated with low levels of norepinephrine , and later researchers theorized that serotonin was the neurotransmitter of interest . In subsequent years, there were numerous attempts to identify reproducible neurochemical alterations in the nervous systems of patients diagnosed with depression. For instance, researchers compared levels of serotonin metabolites in the cerebrospinal fluid of clinically depressed suicidal patients to controls, but the primary literature is mixed and plagued with methodological difficulties such as very small sample sizes and uncontrolled confounding variables. In a recent review of these studies, the chairman of the German Medical Board and colleagues stated, “Reported associations of subgroups of suicidal behavior (e.g. violent suicide attempts) with low CSF–5HIAA concentrations are likely to represent somewhat premature translations of findings from studies that have flaws in methodology” . Attempts were also made to induce depression by depleting serotonin levels, but these experiments reaped no consistent results . Likewise, researchers found that huge increases in brain serotonin, arrived at by administering high-dose L-tryptophan, were ineffective at relieving depression . (Illustration: Margaret Shear, Public Library of Science) Contemporary neuroscience research has failed to confirm any serotonergic lesion in any mental disorder, and has in fact provided significant counterevidence to the explanation of a simple neurotransmitter deficiency. Modern neuroscience has instead shown that the brain is vastly complex and poorly understood . While neuroscience is a rapidly advancing field, to propose that researchers can objectively identify a “chemical imbalance” at the molecular level is not compatible with the extant science. In fact, there is no scientifically established ideal “chemical balance” of serotonin, let alone an identifiable pathological imbalance. To equate the impressive recent achievements of neuroscience with support for the serotonin hypothesis is a mistake. With direct proof of serotonin deficiency in any mental disorder lacking, the claimed efficacy of SSRIs is often cited as indirect support for the serotonin hypothesis. Yet, this ex juvantibus line of reasoning (i.e., reasoning “backwards” to make assumptions about disease causation based on the response of the disease to a treatment) is logically problematic—the fact that aspirin cures headaches does not prove that headaches are due to low levels of aspirin in the brain. Serotonin researchers from the US National Institute of Mental Health Laboratory of Clinical Science clearly state, “he demonstrated efficacy of selective serotonin reuptake inhibitors…cannot be used as primary evidence for serotonergic dysfunction in the pathophysiology of these disorders” . Reasoning backwards, from SSRI efficacy to presumed serotonin deficiency, is thus highly contested. The validity of this reasoning becomes even more unlikely when one considers recent studies that even call into question the very efficacy of the SSRIs. Irving Kirsch and colleagues, using the Freedom of Information Act, gained access to all clinical trials of antidepressants submitted to the Food and Drug Administration (FDA) by the pharmaceutical companies for medication approval. When the published and unpublished trials were pooled, the placebo duplicated about 80% of the antidepressant response ; 57% of these pharmaceutical company–funded trials failed to show a statistically significant difference between antidepressant and inert placebo . A recent Cochrane review suggests that these results are inflated as compared to trials that use an active placebo . This modest efficacy and extremely high rate of placebo response are not seen in the treatment of well-studied imbalances such as insulin deficiency, and casts doubt on the serotonin hypothesis. Also problematic for the serotonin hypothesis is the growing body of research comparing SSRIs to interventions that do not target serotonin specifically. For instance, a Cochrane systematic review found no major difference in efficacy between SSRIs and tricyclic antidepressants . In addition, in randomized controlled trials, buproprion and reboxetine were just as effective as the SSRIs in the treatment of depression, yet neither affects serotonin to any significant degree. St. John's Wort and placebo have outperformed SSRIs in recent randomized controlled trials. Exercise was found to be as effective as the SSRI sertraline in a randomized controlled trial . The research and development activities of pharmaceutical companies also illustrate a diminishing role for serotonergic intervention—Eli Lilly, the company that produced fluoxetine (Prozac), recently released duloxetine, an antidepressant designed to impact norepinephrine as well as serotonin. The evidence presented above thus seems incompatible with a specific serotonergic lesion in depression. Although SSRIs are considered “antidepressants,” they are FDA-approved treatments for eight separate psychiatric diagnoses, ranging from social anxiety disorder to obsessive-compulsive disorder to premenstrual dysphoric disorder. Some consumer advertisements (such as the Zoloft and Paxil Web sites) promote the serotonin hypothesis, not just for depression, but also for some of these other diagnostic categories . Thus, for the serotonin hypothesis to be correct as currently presented, serotonin regulation would need to be the cause (and remedy) of each of these disorders . This is improbable, and no one has yet proposed a cogent theory explaining how a singular putative neurochemical abnormality could result in so many wildly differing behavioral manifestations. In short, there exists no rigorous corroboration of the serotonin theory, and a significant body of contradictory evidence. Far from being a radical line of thought, doubts about the serotonin hypothesis are well acknowledged by many researchers, including frank statements from prominent psychiatrists, some of whom are even enthusiastic proponents of SSRI medications (see Table 1). However, in addition to what these authors say about serotonin, it is also important to look at what is not said in the scientific literature. To our knowledge, there is not a single peer-reviewed article that can be accurately cited to directly support claims of serotonin deficiency in any mental disorder, while there are many articles that present counterevidence. Furthermore, the Diagnostic and Statistical Manual of Mental Disorders (DSM), which is published by the American Psychiatric Association and contains the definitions of all psychiatric diagnoses, does not list serotonin as a cause of any mental disorder. The American Psychiatric Press Textbook of Clinical Psychiatry addresses serotonin deficiency as an unconfirmed hypothesis, stating, “Additional experience has not confirmed the monoamine depletion hypothesis” . Consumer Advertisements of Antidepressants Contrary to what many people believe, the FDA does not require preapproval of advertisements. Instead, the FDA monitors the advertisements once they are in print or on the air . Misleading content is frequently found in various DTCA campaigns ; hence, it is valuable to compare SSRI advertisements to the scientific evidence reviewed above. These SSRI ads are widely promulgated; hundreds of millions of dollars have been spent disseminating these advertisements, and one study found that over 70% of surveyed patients reported exposure to antidepressant DTCA . The Role of the FDA In the US, the FDA monitors and regulates DTCA. The FDA requires that advertisements “cannot be false or misleading” and “must present information that is not inconsistent with the product label” . Pharmaceutical companies that disseminate advertising incompatible with these requirements can receive warning letters and can be sanctioned. The Irish equivalent of the FDA, the Irish Medical Board, recently banned GlaxoSmithKline from claiming that paroxetine corrects a chemical imbalance even in their patient information leaflets . Should the FDA take similar action against consumer advertisements of SSRIs? As just one example, the prescribing information for paroxetine, which is typical of the SSRI-class drugs, states, “The efficacy of paroxetine in the treatment of major depressive disorder, social anxiety disorder, obsessive-compulsive disorder (OCD), panic disorder (PD), generalized anxiety disorder (GAD), and post-traumatic stress disorder (PTSD) is presumed to be linked to potentiation of serotonergic activity in the central nervous system resulting from inhibition of neuronal reuptake of serotonin. Studies at clinically relevant doses in humans have demonstrated that paroxetine blocks the uptake of serotonin into human platelets” . In other words, the mechanism of action of paroxetine has not been definitively established, and remains unconfirmed and presumptive (the prescribing information states that the efficacy of the drug “is presumed to be linked to potentiation of serotonergic activity” (, our italics added). Although there is evidence that paroxetine inhibits the reuptake of serotonin, the significance of this phenomenon in the amelioration of psychiatric symptoms is unknown, and continually debated . Most importantly, the prescribing information does not mention a serotonin deficiency in those administered paroxetine, nor does it claim that paroxetine corrects an imbalance of serotonin. In contrast, the consumer advertisements for paroxetine present claims that are not found in this FDA-approved product labeling. In order to determine whether these advertisements actually comply with FDA regulations, it is useful to consult the Code of Federal Regulations under which DTCA is regulated. The regulations state that an advertisement may be cited as false or misleading if it “ontains claims concerning the mechanism or site of drug action that are not generally regarded as established by scientific evidence by experts qualified by scientific training and experience without disclosing that the claims are not established and the limitations of the supporting evidence…” (, our emphasis added]). Stating that depression may be due to a serotonin deficiency is seemingly allowed, but, as stated in the regulations, only if the limitations of the supporting evidence are provided. In our examination of SSRI advertisements, we did not locate a single advertisement that presented any such information. Instead, the serotonin hypothesis is typically presented as a collective scientific belief, as in the Zoloft advertisement, which states that regarding depression, “Scientists believe that it could be linked with an imbalance of a chemical in the brain called serotonin” . Consumers viewing such advertisements remain uninformed regarding the limitations of the serotonin hypothesis (reviewed above). According to federal regulations, advertisements are also proscribed from including content that “contains favorable information or opinions about a drug previously regarded as valid but which have been rendered invalid by contrary and more credible recent information” . This means that a disconnect between the evolving peer-reviewed literature and advertisements is not permitted. Regarding SSRIs, there is a growing body of medical literature casting doubt on the serotonin hypothesis, and this body is not reflected in the consumer advertisements. In particular, many SSRI advertisements continue to claim that the mechanism of action of SSRIs is that of correcting a chemical imbalance, such as a paroxetine advertisement, which states, “With continued treatment, Paxil can help restore the balance of serotonin…” . Yet, as previously mentioned, there is no such thing as a scientifically established correct “balance” of serotonin. The take-home message for consumers viewing SSRI advertisements is probably that SSRIs work by normalizing neurotransmitters that have gone awry. This was a hopeful notion 30 years ago, but is not an accurate reflection of present-day scientific evidence. The FDA has sent ten warning letters to antidepressant manufacturers since 1997 , but has never cited a pharmaceutical company for the issues covered here. The reasons for their inaction are unclear but seem to result from a deliberate decision at some level of the FDA, rather than an oversight. Since 2002, the first author (JRL) has repeatedly contacted the FDA regarding these issues. The only substantive response was an E-mail received from a regulatory reviewer at the FDA: “Your concern regarding direct-to-consumer advertising raises an interesting issue regarding the validity of reductionistic statements. These statements are used in an attempt to describe the putative mechanisms of neurotransmitter action(s) to the fraction of the public that functions at no higher than a 6th grade reading level” (personal communication, 2002 April 11). It is curious that these advertisements are rationalized as being appropriate for those with poor reading skills. If the issues surrounding antidepressants are too complex to explain accurately to the general public, one wonders why it is imperative that DTCA of antidepressants be permitted at all. However, contrary to what the FDA seems to be implying, truth and simplicity are not mutually exclusive. Consider the medical textbook, Essential Psychopharmacology, which states, “So far, there is no clear and convincing evidence that monoamine deficiency accounts for depression; that is, there is no ‘real’ monoamine deficit” . Like the pharmaceutical company advertisements, this explanation is very easy to understand, yet it paints a very different picture about the serotonin hypothesis. Conclusion The impact of the widespread promotion of the serotonin hypothesis should not be underestimated. Antidepressant advertisements are ubiquitous in American media, and there is emerging evidence that these advertisements have the potential to confound the doctor–patient relationship. A recent study by Kravitz et al. found that pseudopatients (actors who were trained to behave as patients) presenting with symptoms of adjustment disorder (a condition for which antidepressants are not usually prescribed) were frequently prescribed paroxetine (Paxil) by their physicians if they inquired specifically about Paxil ; such enquiries from actual patients could be prompted by DTCA . What remains unmeasured, though, is how many patients seek help from their doctor because antidepressant advertisements have convinced them that they are suffering from a serotonin deficiency. These advertisements present a seductive concept, and the fact that patients are now presenting with a self-described “chemical imbalance” shows that the DTCA is having its intended effect: the medical marketplace is being shaped in a way that is advantageous to the pharmaceutical companies. Recently, it has been alleged that the FDA is more responsive to the concerns of the pharmaceutical industry than to their mission of protecting US consumers, and that enforcement efforts are being relaxed . Patients who are convinced they are suffering from a neurotransmitter defect are likely to request a prescription for antidepressants, and may be skeptical of physicians who suggest other interventions, such as cognitive-behavioral therapy , evidence-based or not. Like other vulnerable populations, anxious and depressed patients “are probably more susceptible to the controlling influence of advertisements” . In 1998, at the dawn of consumer advertising of SSRIs, Professor Emeritus of Neuroscience Elliot Valenstein summarized the scientific data by concluding, “What physicians and the public are reading about mental illness is by no means a neutral reflection of all the information that is available” . The current state of affairs has only confirmed the veracity of this conclusion. The incongruence between the scientific literature and the claims made in FDA-regulated SSRI advertisements is remarkable, and possibly unparalleled. References 1. Mintzes B (2002) For and against: Direct to consumer advertising is medicalising normal human experience: For. BMJ 324: 908–909. Find this article online 2. International Marketing Services Health (2004) Year-end U.S. Prescription and sales information and commentary. Fairfield. (Connecticut): International Marketing Services Health Available: http://www.imshealth.com/ims/portal/front/articleC/0,2777,6599_3665_69890098,00.html. Accessed 14 October 2005. 3. Donohue J, Berndt E (2004) Effects of direct-to-consumer advertising on medication choice: The case of antidepressants. J Pub Pol Marketing 23: 115–127. Find this article online 4. United Kingdom Parliament (2005) House of Commons health report. London: United Kingdom House of Commons. Available: http://www.publications.parliament.uk/pa/cm200405/cmselect/cmhealth/42/4202.htm. Accessed 14 October 2005. 5. Pfizer (2004 March) Zoloft advertisement. Burbank (California): NBC. 6. Schildkraut JJ (1965) The catecholamine hypothesis of affective disorders: A review of supporting evidence. J Neuropsychiatry Clin Neurosci 7: 524–533. Find this article online 7. Coppen A (1967) The biochemistry of affective disorders. Br J Psychiatry 113: 1237–1264. Find this article online 8. 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Washington (D.C.): American Psychiatric Press. pp 439–542. 26. Consumer Reports (2003) Free rein for drug ads. Yonkers (New York): Consumer Reports Available: http://www.consumerreports.org/main/detailv2.jsp?CONTENT%3C%3Ecnt_id=299631&FOLDER%3C%3Efolder_id=162687. Accessed 14 October 2005. 27. United States General Accounting Office (2002) Prescription drugs: FDA oversight of direct-to-consumer advertising has limitations. Washington (D.C.): United States General Accounting Office. Available: http://www.gao.gov/new.items/d03177.pdf. Accessed 2005 February 19. 28. Mintzes B, Barer ML, Kravitz RL, Basett K, Lexchin J, et al. (2003) How does direct-to-consumer advertising (DTCA) affect prescribing? A survey in primary care environments with and without legal DTCA. CMAJ 169: 405–412. Find this article online 29. O'Brien C (2003 October 5) Drug firm to drop non-addiction claim. Irish Times. 30. GlaxoSmithKline (2005) Paxil Prescribing Information. Research Triangle Park (North Carolina): GlaxoSmithKine. Available: http://us.gsk.com/products/assets/us_paxil.pdf. Accessed 14 October 2005. 31. Castren E (2005) Is mood chemistry? Nat Rev Neuroscience 6: 241–226. Find this article online 32. Food and Drug Administration (2005) Code of federal regulations, 21CFR202. Title 21—Food and drugs. Chapter I—Food and drug administration. Department of Health and Human Services. Part 202—Prescription-drug advertisements. Available: http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?CFRPart=202&showFR=1. Accessed 14 October 2005. 33. Pfizer (2005) Learning about depression: What causes depression. Cambridge (Massachusetts): Pfizer. Available: http://www.zoloft.com/zoloft/zoloft.portal?_nfpb=true&_pageLabel=depr_causes Accessed 17 October 2005. 34. Food and Drug Administration Division of Drug Marketing Advertising and Communications (1997) Effexor warning letter. Rockville (Maryland): Food and Drug Administration. Available: http://www.fda.gov/cder/warn/june97/effexor.pdf. Accessed 14 October 2005. 35. Food and Drug Administration Division of Drug Marketing Advertising and Communications (1998) Paxil warning letter. Rockville (Maryland): Food and Drug Administration. Available: http://www.fda.gov/cder/warn/mar98/6383.pdf. Accessed 14 October 2005. 36. Food and Drug Administration Division of Drug Marketing Advertising and Communications (1999) Remeron warning letter. Rockville (Maryland): Food and Drug Administration. Available: http://www.fda.gov/cder/warn/jan99/6950.pdf. Accessed 2005 May 9. 37. Food and Drug Administration Division of Drug Marketing Advertising and Communications (2000) Sarafem warning letter. Rockville (Maryland): Food and Drug Administration. Available: http://www.fda.gov/cder/warn/nov2000/dd9523.pdf. Accessed 14 October 2005. 38. Food and Drug Administration Division of Drug Marketing Advertising and Communications (2000) Effexor warning letter. Rockville (Maryland): Food and Drug Administration. Available: http://www.fda.gov/cder/warn/oct2000/dd8741.pdf. Accessed 14 October 2005. 39. Food and Drug Administration Division of Drug Marketing Advertising and Communications (2000) Remeron warning letter. Rockville (Maryland): Food and Drug Administration. Available: http://www.fda.gov/cder/warn/apr2000/dd8496.pdf. Accessed 14 October 2005. 40. Food and Drug Administration Division of Drug Marketing Advertising and Communications (2002) Celexa warning letter. Available: http://www.fda.gov/cder/warn/2002/10853Celexa.pdf. Accessed 14 October 2005. 41. Food and Drug Administration Division of Drug Marketing Advertising and Communications (2004) Effexor warning letter. Rockville (Maryland): Food and Drug Administration. Available: http://www.fda.gov/cder/warn/2004/Effexor.pdf. Accessed 14 October 2005. 42. Food and Drug Administration Division of Drug Marketing Advertising and Communications (2004) Paxil warning letter. Rockville (Maryland): Food and Drug Administration. Available: http://www.fda.gov/cder/warn/2004/MACMIS12439.pdf. Accessed 14 October 2005. 43. Food and Drug Administration Division of Drug Marketing Advertising and Communications (2005) Zoloft warning letter. Rockville (Maryland): Food and Drug Administration. Available: http://www.fda.gov/cder/warn/2005/zoloft_letter.pdf. Accessed 14 October 2005. 44. Stahl SM (2000) Essential psychopharmacology: Neuroscientific basis and practical applications. Cambridge: Cambridge University Press. 601 p. 45. Kravitz RL, Epstein RM, Feldman MD, Franz CE, Azari R, et al. (2005) Influence of patients' requests for direct-to-consumer advertised antidepressants: A randomized controlled trial. JAMA 293: 1995–2002. Find this article online 46. Kramer TAM (2002) Endogenous versus exogenous: Still not the issue. MedGenMed 4 Available: http://www.medscape.com/viewarticle/418269. Accessed 14 October 2005. 47. Angell M (2004) The truth about the drug companies: How they deceive us and what to do about it. New York: Random House. 336 p. 48. DeRubeis R, Hollon S, Amsterdam J, Shelton R, Young P, et al. (2005) Cognitive therapy vs medications in the treatment of moderate to severe depression. Arch Gen Psychiatry 62: 409–416. Find this article online 49. Hollon MF (2004) Direct-to-consumer marketing of prescription drugs: A current perspective for neurologists and psychiatrists. CNS Drugs 18: 69–77. Find this article online 50. Valenstein ES (1998) Blaming the brain: The truth about drugs and mental health. New York: Free Press. 292 p. 51. Glenmullen J (2001) Prozac backlash: Overcoming the dangers of prozac, zoloft, paxil and other antidepressants with safe, effective alternatives. New York: Simon and Schuster. 384 p. 52. Delgado P, Moreno F (2000) Role of norepinephrine in depression. J Clin Psychiatry 61. Supple 1 5–11. Find this article online 53. Kramer P (2002 July 7) Fighting the darkness in the mind, July 7. The New York Times Sect 4 8. 54. Lacasse JR, Gomory T (2003) Is graduate social work education promoting a critical approach to mental health practice? J Soc Work Educ 39: 383–408. Find this article online 55. Healy D (2004) Let them eat prozac: The unhealthy relationship between the pharmaceutical companies and depression. New York: New York University. 351 p. 56. Kendler KS (2005) Toward a philosophical structure for psychiatry. Am J Psychiatry 162: 433–440. Find this article online 57. Forest Pharmaceuticals (2005) Frequently asked questions. New York: Forest Pharmaceuticals. Available: http://www.celexa.com/Celexa/faq.aspx. Accessed 17 October 2005. 58. Forest Pharmaceuticals (2005) How Lexapro (escitalopram) works. New York: Forest Pharmaceuticals. Available: http://www.lexapro.com/english/about_lexapro/how_works.aspx. Accessed 17 October 2005. 59. Eli Lilly (1998 January) Prozac advertisement. People Magazine: 40. 60. GlaxoSmithKline (2001 October) Paxil advertisment. Newsweek: 61. | |
Posted by Linda, 11:28 25 March 2007Depressed or anxious? Switching pills for your ills a dangerous
practice by Alan Cassels The story of benzodiazepines is of awesome proportions... a national scandal. The impact is so large that it is too big for governments, regulatory authorities and the pharmaceutical industry to address head-on, so the scandal has been swept under the carpet. Phil Woolas MP, British House of Commons, December 7, 1999. In Selling Sickness, Ray Moynihan and I discussed how the pharmaceutical industry, ever vigilant to expand new markets for its products, has worked in tandem with the medical profession to widen the boundaries of illness. We described a world where "new" conditions are painted as "dire," and where risk factors in our bones or blood are promoted to full-fledged diseases, in and of themselves, hence becoming prime targets for pharmaceutical intervention. In painting this picture, however, we touched only briefly on a very important aspect of selling sickness: the methodologies used to shift patients from older, cheaper, off-patented drugs to newer and more expensive patented products. The best example to demonstrate this phenomenon is the recharacterization of anxiety into depression and the wholesale switching of older, anti-anxiety drugs, largely benzodiazepines -- drugs like Ativan, Valium and Xanax -- to newer SSRIs, selective serotonin reuptake inhibitors, such as Paxil, Zoloft or Prozac. The switch to newer treatments is partially due to the "newer is better" thinking that permeates so much of our consumer culture. The fact that older drugs tend to carry more baggage also has a lot to do with it. We have learned about those drugs and their warts and blemishes simply because we have had more experience with them. Shifting patients from more established and better understood therapies to newer ones that we have less knowledge about may sometimes have a strong medical rationale. It may be because there is a clearer understanding of the condition. An older drug's side effects may be intolerable, with the newer one marketed as being "safer." Any extra cost involved may seem justified. But switching patients' drugs is a potentially dangerous practice, which may accomplish nothing more than exchanging one set of problems for another. According to the British Medical Journal, "The growing search for blockbusters in the 1970s resulted in a trend to rubbish earlier drugs in order to put new patent-protected drug classes on the market." The BMJ points out that, in the case of treatments for mood and anxiety disorders, "Despite clear evidence that benzodiazepines were effective, they were dismissed as drugs for neurotic women, who then become addicted." After a brief flirtation with tricyclic antidepressants, which were also quickly considered to have too many adverse effects, the world bent to embrace the brave new world of the SSRI antidepressants. In the 1960s, drug companies were not at all interested in depression; they didn't think it was marketable. (David Healy's books, including Let Them Eat Prozac, lay this out in fine detail). Depression was considered an easily self-cured problem, so the real market was always anxiety. With the rise of the SSRIs in the mid '80s, depression became the drug makers' ultimate target, and the sales of anti-anxiety drugs plummeted. Since 1990, no drugs patented in the mood and anxiety area have reached the US market. I decided that in order to dig deeper into this issue, I needed to see the "switching" phenomenon in action. A great opportunity arrived via email when I was invited to participate in an online course for pharmacists to learn about new treatments for panic disorder. Now, I'm all for continuing education. I enjoy taking courses that are designed for pharmacists, not because I'm a pharmacist, but because as a pharmaceutical policy researcher I have a deep interest in knowing what pharmacists are learning: what kinds of messages they are getting about new diagnoses, and how the effects and side effects of new treatments are conveyed to them. In many ways, pharmacists are among the most underappreciated members of the medical team. For many consumers, the first place they go for medical advice, or to ask a question about a drug, is the pharmacy. Pharmacists do what is arguably one of the most important jobs in the medical system: they try to get people to use prescription drugs properly. In this vein, I took an online course in the treatment of panic disorder designed for pharmacists. Continuing pharmacy education (CPE) is like continuing legal education (CLE) for lawyers, or continuing medical education (CME) for doctors, an important way for professionals to stay on top of new developments in their discipline. Although a pharmacist doesn't write prescriptions, her job is to make sure that people use dispensed pharmaceuticals in an informed and intelligent way. She therefore requires up-to-date, professional education to help her better counsel people to avoid drug related problems. The CPE module taught me a lot about panic disorder, but it wasn't panic disorder, per se, that fuelled my curiosity. What I was really interested in, was why a drug company, through an "unrestricted educational grant" was spending thousands of dollars to support this module. What was in it for the company? I mean, pharmacists can't prescribe. The module set-up provided some clues. The program featured a "case study" of a woman in her late 20s, who was taking a drug called alprazolam (also known as Xanax) to deal with her panic disorder. Xanax is a classic benzodiazepine that has been around for at least 40 years, and is often prescribed for anxiety or sleep disorders. In 1981, alprazolam was the first medication approved for panic disorder, yet some experts question whether panic disorder was even a diagnosable illness, distinct from other kinds of mental illness. But let's put that controversy aside for a bit. The case study was set up with the woman showing obvious signs of panic. She chokes and has difficulty breathing. She sweats and has clammy hands. She had just returned from visiting her psychiatrist, who suggested she try Effexor (venlafaxine), a newer SNRI (serotonin noradrenalin re-uptake inhibitor). Ah, there's the rub. The patient wants the pharmacist's advice on whether she should be switched to Effexor, a newer, more expensive treatment made by -- whoa, wait a minute, that's the same company that's paying for this pharmacy education module I'm working on. OK, it's starting to make some sense. So let's assume Effexor "works" for panic disorder. What is the rationale for switching someone from one drug to another? The learning module characterizes it in this way: "Antidepressants are often first-line for panic disorder because of their broad spectrum efficacy against common co-morbid conditions including depression..." and "the lack of associated abuse and dependency liabilities that are associated with benzodiazepine administration." Allow me to translate: The reason we are recommending that you switch from a benzo to an SSRI or SSNI is because these newer ones are effective against other things you might have while you are depressed and because the benzos are addictive. According to UK-based physician C. Heather Ashton, one of the leading experts on benzodiazepines, as many as half of long-term benzo users may be able to stop without symptoms, but it depends on how long one has taken them. If someone has taken them for a year or so, she is likely dependent, and ending that dependence can mean severe, serious withdrawal effects that require weaning and individualized tapering. Some have said that withdrawing from benzos is like having four or five other diseases at the same time. People experience anxiety, insomnia, irritability, gut-wrenching stomach cramps, or sensitivity to light and noise. They can become confused, depersonalized, delirious, psychotic and insomniac. It can be nasty, nasty stuff. Luckily, the learning module does include some helpful information on trying to wean people off benzos -- and a pharmacist can be really helpful here -- but quitting can be a long, frustrating and difficult process. In our case study, the patient is being encouraged to move to Effexor, but what kinds of side effects might be expected? The approved product labelling for Effexor notes that it is also associated with potentially severe withdrawal side effects, which could include fatigue, nausea, dizziness, headache, insomnia and nervousness. In fact, symptoms of withdrawal can be so significant that in March 2000, the US FDA ordered Effexor's manufacturer Wyeth-Ayerst to add additional labeling: "Abrupt discontinuation or dose reduction of venlafaxine at various doses has been found to be associated with the appearance of new symptoms, the frequency of which increased with increased dose level and with longer duration of treatment... It is therefore recommended that the dosage of Effexor be tapered gradually and the patient monitored." In case I've lost you, remember this: weaning yourself off Xanax so that you can be moved to Effexor may mean a whole new set of nasty withdrawal effects. Sounds eerily like we are trading one set of symptoms for a whole 'nuther set. There is also the issue of suicide. One of the original reasons to get people off benzos was because the drugs could be the cause of suicide by overdose. This has always struck me as a red herring, an inducement to get people to switch to the newer stuff. But let's look at the information Health Canada released in June 2003: "Health Canada is advising Canadians that all newer anti-depressant prescription drugs, known as selective serotonin re-uptake inhibitors (SSRIs) or serotonin noradrenalin re-uptake inhibitors (SNRIs), now carry stronger warnings. These new warnings indicate that patients of all ages taking these drugs may experience behavioural and/or emotional changes that may put them at increased risk of self-harm or harm to others. In other words, the two concerns prompting a switch from benzos -- addiction and suicide -- also apply to the recommended replacement drug. Depression is one of the fastest rising diagnoses made by office-based physicians; visits to a physician for depression have almost doubled since 1994. Furthermore, in 2004, 81 percent of depression-related visits resulted in a recommendation for an SSRI or a related drug, and the cost impact has been enormous. From 1993 to 2000, drug sales have increased 347 percent, and we have seen an increase in prescriptions for both benzos and SSRIs. In BC, from 1996 to 2002, benzo use increased by 11 percent, yet the use of antidepressants increased by 73 percent over the same time period. Janet Currie of Victoria is probably one of Canada's leading experts on benzodiazepines and the effects of SSRIs. She recently wrote a report entitled The Marketization of Depression: the Prescribing of SSRI Antidepressants to Women (see www.whp-apsf.ca/pdf/SSRIs.pdf), wherein she notes that the drugging of depression and anxiety is largely a female issue, since two-thirds of SSRI users are women. Further, "The clinical trial results for SSRIs raise many questions about their effectiveness, and yet hundreds of thousands of Canadian women are being exposed to these potent brain chemicals, sometimes for many, many years despite their many risks and side effects." She would agree that shifting patients from benzos to antidepressants is not just costly, resulting in huge profits to big pharma, but it often ignores the alternatives, such as talking to someone or engaging in exercise therapy, both which may be effective as non-drug treatments for anxiety or depression. Currie reminds me that history can be seen to continually repeat itself. Citing the 10-20-30 rule -- that it takes us about 30 years to realistically view a class of drugs in its entirety, both the benefits and the harms -- she points to Joseph Glenmullen's book The Antidepressant Solution: A Step by Step Guide to Safely Overcoming Antidepressant Withdrawal, Dependence and Addiction. Following the arrival of a new class of drugs on the market, it takes at least a decade for physicians to even become aware of its most serious side effects, partially due to the fact that regulatory agencies such as Health Canada have such weak systems for monitoring side effects. When serious effects are noted, the pharmaceutical companies go into denial, and it takes another decade to actually collect enough data and study what the serious problems may be. Although patient advocates are now sounding the alarm, it will take another decade before regulatory agencies and professional organizations act to change treatment guidelines and prescribing patterns. By that time, 30 years hence, what was "new" has become old, and drug companies have come out with an even "newer" -- read more patented and therefore profitable -- drug. We have seen this with the benzos and the tricyclics, and we're starting to see the same pattern with the SSRIs, as new treatments, such as Effexor, arrive. Currie sees that one of the biggest holes in the health system is its failure to provide people the help to get off unneeded or harmful drugs like the addictive benzodiazepines. She helped start the Psychiatric Medication Awareness Group (www.psychmedaware.org), and is one of the West Coast's brightest lights for raising awareness and disseminating knowledge about psychiatric drugs. While my online pharmacy module may guide pharmacists to address the issue of dependence and withdrawal for drugs like Xanax, in Canada, no government-funded services are available to help people safely withdraw from benzodiazepine addiction. While you're basically on your own, you could get in touch with groups around the world doing this work as part of the benzo awareness network. Two notable groups are www.benzo.org.uk, a UK-based group focused on benzodiazepine addiction, withdrawal and recovery, and Tranquilliser Recovery and New Existence (TRANX) in Australia, www.tranx.org.au. The pharmacy module dryly sums up the situation: The "...present case serves to illustrate the potential severity of alprazolam rebound and how its long-term use can exacerbate the symptoms for which it was originally administered." Fine enough, but what about Effexor's side effects? Is it actually useful for panic disorder? Listed side effects for Effexor include anxiety, agitation, panic attacks, insomnia, irritability, hostility, aggressiveness, impulsivity, akathisia (psychomotor restlessness), hypomania and mania. Alan Cassels is the co-author of Selling Sickness: How the World's Biggest Pharmaceutical Companies Are Turning Us All into Patients, and a drug policy researcher at the University of Victoria. He has spent most of the last 10 years studying how clinical research about prescription drugs is communicated to policy makers, prescribers and consumers. He is also the founder of Media Doctor Canada (www.mediadoctor.ca), which evaluates the reporting of medical treatments in Canada's media | |
Posted by darrellisgrumpy, 12:38 25 March 2007This "log" is maintained by someone who has not got any medical qualifications. It should in my opinion be viewed with great care as it does not make any efforts to show that medication has a good and needed place in our modern society.
My advice is always to talk with your GP about any thoughts you have about the use of medication. I too have no medical qualifications and have had some poor experiences with medication. However, there comes a point at which a crusade to enlighten and inform passes over a threshold of reason an into the realms of obsession. Keep an open mind about all things. Be reasonable about your thoughts and expectations and above all else keep your own counsel. | |
Posted by Linda, 21:08 25 March 2007Dr. Breggin's resume can be viewed here:
http://www.breggin.com/resume.html | |
Posted by Linda, 16:15 26 March 2007If you read nothing else here, please at least read this. It is this kind of info that blew my mind after years of growing up believing that the doctor always knows best, and that the drugs he/she prescribes can be trusted to help me. It encapsulates pretty much EVERYTHING I have been saying in this topic. I hope this empowers everyone who read it.
from NewsTarget.com Tuesday, June 07, 2005 by Mike Adams, editor Big Tobacco and Big Pharma: Same Tactics, Different Chemicals Have you ever thought about the similarities between pharmaceutical and tobacco companies? They're striking. Both sell products that kill people when used as directed. The statistics are readily available for pharmaceuticals, which kill around 100,000 Americans each year according to the Journal of the American Medical Association, and Big Tobacco, which makes tobacco products that are partly responsible for hundreds of thousands of cases of cancer in the United States each year. These are the facts from industry. Industry critics (such as myself) would argue that those numbers are actually much higher. But let's look at other similarities. Aside from marketing products that actually kill people when used as directed, both industries are engaged in the blatant distortion of scientific evidence in order to mislead regulators and the public. With Big Tobacco we saw the suppression of studies that said nicotine was addictive, or of studies linking the inhalation of tobacco smoke to lung cancer. In the pharmaceutical industry, we see even worse distortions of clinical studies. We see studies that are designed to minimize the appearance of negative risks associated with these drugs, such as heart attacks , stroke, mental disorders, suicide attempts, and violent behavior. Even after studies are completed, the results are highly distorted as well. Drug companies pick and choose which studies they want to publish. They may do twelve different studies on a particular drug, and if six of them say the drug is safe and effective, while the other six studies say the drug is dangerous and useless from a medicinal point of view, they pick the six they want and bury the others. They forward the six they want to the FDA. The FDA looks at those six and says, "This sure is scientific!", and they approve that drug application. I'm not making this up. In the late 1990's, drug advertising appeared on television. That is, of course, another similarity between Big Tobacco and Big Pharma: they both use direct-to-consumer advertising to create demand for their products. For many years, tobacco companies sponsored sporting events; in fact, they still attempt to sponsor many sporting events. In the pharmaceutical industry, we see heavy magazine and television advertising, and hundreds of millions of dollars spent lobbying doctors , buying them gifts, trips (to Hawaii, believe it or not), air tickets, and stays in luxurious resorts. All doctors have to do is show up, sign in, and act like they're attending a continuing medical education course. They then can leave for the entire day, and go on the beach, go fishing, go surfing, and do whatever they want. It's an all-expenses-paid vacation. Some people say, "No, that's ridiculous. That doesn't happen." I've actually been in Hawaii, talking to doctors who were attending such an event. I saw the entire room of about four hundred MD's, and these people just signed in, then they left to go surfing with me! So I know how the system works, I've seen it firsthand. All the doctors out there who might be listening to this, you know how it works too. A lot of these continuing medical education courses are really just a joke. Doctors pushed cigarettes for decades Another interesting similarity between cigarettes and prescription drugs is that doctors have a history of supporting them both very strongly. You might say, "Wait a minute, doctors don't support smoking and cigarettes." Sure they do, if you just go back far enough. In the seventies and eighties, they began to figure out that smoking is bad for you. Before that, however, doctors could actually be found as spokespersons for cigarettes. They said that cigarettes made you healthy. You can find, in archives of old magazines like Time, that some doctors are even in advertisements stating, "Smoking, it's good for your smile". They also said smoking helps you concentrate, and that it's good for your nervous system. They made many ridiculous claims about cigarettes. We tend to forget about that today, but doctors were paid to be spokespersons for tobacco companies, and this went on for decades. Today, of course, old school doctors are strongly in support of prescription drugs. But new doctors, the smart doctors, whom I hope you're visiting, are questioning the safety of prescription drugs. They are looking outside of conventional medicine for solutions, in terms of disease prevention and even the simple treatment of symptoms. These new doctors are noticing that people get healthier when they get off of prescription drugs. Alternatively, they use prescription drugs only as a temporary measure in order to give the patient enough time and education so that they can put into effect long term lifestyle changes that, in turn, eliminate the need for the drugs. Of course, this frustrates the drug companies, since they want people to take these drugs for a lifetime. They claim that it's good for you, but actually, it's only good for their bottom line when you become a daily user of their overpriced product. Good doctors are recognizing that. They recognize statin drugs do have a temporary role in dealing with an acute symptom, which might be extremely elevated cholesterol that represents an immediate risk to the person's health or even life. So they may use a statin drug on a temporary basis, only for a few weeks or a couple of months at most. They meanwhile help patients undergo major, fundamental reforms in their lifestyle consisting of food choice, dietary habits, and physical exercise, avoidance of environmental toxins, lower levels of chronic stress, better sleep, better hormonal balance, and so on. Marketing to children Here's another similarity between Big Tobacco and Big Pharma: They both love to market to children. For years, tobacco companies have been trying to edge and wiggle their way into the adolescent market, targeting teenagers and children. They used Joe Camel, a cartoon character, to sell cigarettes, because they knew that if they could get adolescents hooked on nicotine, they had a customer for life. It's not rocket science to figure out the marketing tactic there for Big Tobacco. Pharmaceutical companies don't have the same addictive quality for their drugs. You're not necessarily psychologically or physiologically addicted to drugs in the same way as nicotine. However, by starting a kid early on drugs, they can create a paradigm where that kid grows up thinking that he is a diseased person, and that he is that label. So if they get a kid diagnosed as ADD or ADHD, then that child will associate that label with himself or herself, and will continue on in life with the belief that they have some sort of disease or brain chemical imbalance. And they'll even tell other people, "I'm ADD" or "I'm bipolar," as if that's who they are. That, of course, is not who they are. That's a completely fictitious label; it's been made up, and it's been placed upon them. But the trick is that by placing these labels upon these children, the drug companies know that when those children grow up, they identify themselves with those diseases, and they readily accept the idea of taking more prescription drugs as long as the doctors put more labels on them. So as they grow up, they'll find more labels, being told, "You have a syndrome X, you need this drug" or "You have high blood pressure and that's a disease, so you need this drug to lower your blood pressure." If you take a child and you get them used to the idea of associating their identity with labels of diseases, then you create a lifelong customer for the pharmaceutical industry. Big Pharma knows this, and their marketing people understand this. Some people will do anything for a paycheck Another interesting similarity between Big Tobacco and Big Pharma is that both are staffed by people you might consider to be ordinary, everyday people. They might be your neighbors, people that you wouldn't think would be harmful, and who aren't necessarily evil. They're just regular, everyday people trying to succeed in their jobs. Yet, they are part of a machine that is creating tremendous pain and suffering, along with destruction, disease, and distortion in our society. It makes you wonder, what kind of people would go work for tobacco companies? Who would do that? What kind of person would go work for a pharmaceutical company? Who are these drug reps? I've met a lot of these drug reps. They're everyday, nice people; people you might have as friends. Maybe you are a drug rep because you just needed a job. But I think it's important to note that there's a great tendency for human beings, when they need jobs, to set aside their ethics. They tend to dissociate themselves from the long term effects of what they are doing. Historically, we saw this of course in Nazi Germany, where people were members of the Nazi party. They were part of a machine that was creating tremendous evil, pain and suffering, and destruction in many different ways. (I'm not talking just about the Holocaust here.) They were part of this machine, yet they felt the need to succeed in their particular role in that machine. They dissociated themselves from the pain and suffering the machine was ultimately causing. Perhaps they saw themselves as just a cog in a big wheel. Maybe they felt like they just had no other options. I suspect that some of the same psychology is at work today in people who work for pharmaceutical companies, or people who work for tobacco companies. But this psychological deception is harder to do today, at least when working for tobacco companies. It's hard to lie to yourself and say, "This is a healthy product." You'd have to be living in some alternate universe, where you've seen none of the science about how dangerous cigarette smoke is to human health. In the pharmaceutical industry, however, there are a lot of people who are lying to themselves, and it's easier to lie to yourself saying, "We are searching for the cure for cancer!" or "We're going to solve osteoporosis and we're going to end suffering!" They think they're part of a machine that's going to end suffering. Thus, they think if they succeed in marketing and creating more money and more profits for their company, then fund more research, they can find all these solutions to disease. Thus, they fall for something I call "The Big Lie," which is the idea that we can solve health problems by creating ever more technologically advanced or complex synthetic chemicals and compounds that, if introduced into the human body, can suddenly reverse all of these diseases which have been created by years and years of abuse through lifestyle, lack of nutrition, exposure to environmental toxins, and so on. The Big Lie of the pharmaceutical industry It's a big lie that you can cure cancer or diabetes by coming up with the right chemical, or that you can even cure depression by altering brain chemistry with the right chemical. This is a big lie. It's as if medical science has gone down the wrong pathway for so long that they can't even see the fact that they're lost. They're lost in the forest, and they can't even see the trees. All they can do is continue to try to come up with more and more chemicals they think are treating these diseases. They think the only reason they haven't cured cancer yet is because they don't have enough money, that it's just a money problem. "Give us more money and in a couple more years, and we'll have cancer cured." That's been the promise they've held out for decades. The reason they think they can cure these diseases if they just have enough money and enough time is because conventional medicine remains stuck in the paradigm of germ theory. And the germ theory says that every disease is based on an organism or an invading element, whether it is a virus or bacteria, and if you just have the right chemical compound, then you can cure that infectious disease. Of course, this was quite valid in the day of penicillin, and it's still valid today for basic, simple infections. But the germ theory does not apply to chronic, degenerative diseases such as cancer, osteoporosis, Alzheimer's disease, arthritis, diabetes, cardiovascular heart disease, Crohn's disease, clinical depression , inflammatory diseases, and so on. Chemical-based medicine is a Newtonian view of health That model of germ theory simply does not apply today. It doesn't mean that germ theory is false, but these chronic degenerative diseases exist in a different realm. For example, regarding physics and the laws of motion, Newtonian physics operate on a large scale; it talks about the interaction between the motion of objects and gravity and momentum. That is a very valid realm of physics and science. And it creates predictable observations and outcomes that match the mathematics. But when you go into quantum mechanics, or when you get to the subatomic level, the rules begin to change. You're now dealing with quantum physics. Quantum physics disagrees with Newtonian physics. But it doesn't mean that quantum physics is wrong, or that Newtonian physics is wrong, it's only that it's applied in a different context. The same is true with medicine. We still have the old germ theory, which I equate to Newtonian physics, trying to be applied to today's epidemic diseases, which shouldn't even be called diseases, because invading microorganisms do not cause them. They are created as a result of many different inputs, or causes that the patient undergoes, or those which the patient chooses to engage in. To call them diseases is really not accurate. Therefore, the idea that you can cure or reverse these fictitious diseases is invalid at its very premise. Cancer is no infectious disease The idea that you can reverse cancer by taking a synthetic chemical compound or prescription drug is, at its very core, nonsense. Because there is no such infectious disease as "cancer," there is no microbial invader. In fact, there isn't even a tissue or a physical element that you can point to and look at under a microscope and say, "That is cancer." Some people mistakenly say, "Well, sure you can. You can take a tumor out of the body, and you can put that under a microscope and call it cancer. However, that's not cancer. That's the side effect of cancer, because cancer is a systemic failure of the immune system. It's a systemic disease. It is actually a condition. It is a lack of the body's ability to self-regulate its own cell growth, to clean up its own blood, tissues, bones, bone marrow, and so on. This is the nature of cancer; you can't put that under a microscope and look at it. In the germ theory of disease, however, scientists are always trying to look at cancer under a microscope, where they can put it down and say, "This is the microbe, see? There's the virus" or "There's the bacteria" or "There's the parasite." They still try to do that today by saying, "Alzheimer's is based on the nervous system. Put it under a microscope and there you can see plaque. Plaque on the nervous system." They think that's the cause of the disease. It's not, it's just a side effect. Big Pharma = big-time poverty Getting back to the main point of this, which is Big Tobacco and Big Pharma, we were talking about why people work for these organizations when these organizations are actually doing such evil, or engaging in the creation of such pain and suffering, and even death. Here in the United States, we're also talking about economic poverty created by both of these companies. Tobacco companies make people poor, because they hook them on a product that's expensive to buy; and they have to keep buying it, because they're addicted to it. You'll notice that people who smoke tend to be on a lower economic scale. Part of that is the vicious feedback cycle; if you start smoking, you will get poorer. As you get poorer, you will continue to smoke more because life is terrible and you need your nicotine high just to feel okay. Thus, it's a downward spiral into oblivion. Much the same is true with prescription drugs in terms of the economic scale and the loss of good, clear decision making abilities. One thing I've noticed is that when people begin taking prescription drugs, not only do they immediately suffer a big economic hit (remember that 50 percent of all bankruptcies in the United States today are due to medical bills, including prescription drugs), they also tend to lose the ability to make good decisions. Many of these drugs, especially statin or antidepressant drugs, for example, affect people's mental acuity. They result in a loss of lucidity, which results in people no longer comprehending the big picture, and no longer making good decisions. When people can't make good decisions, they ultimately decide to allow the doctor to keep prescribing them more prescription drugs. They don't have the mental awareness to say no to the drugs. They keep taking more drugs, and they lose even more awareness. They get even less responsive, and retain less decision-making ability, and this just becomes another downward spiral. As this is happening; they are being drained of their finances. So day after day dollars are leaving their pockets and being stuffed into the pockets of the corporate CEOs and the shareholders of the pharmaceutical companies. There's this huge transfer. Imagine dollar bills with little wings flying out of the pockets of people all around the country and flying into the corporate CEOs' pockets in the big buildings of the giant pharmaceutical companies of this country. That is happening every single day. I believe it's an exploitation of people for economic gain, for greed, by the pharmaceutical companies. Profits first, people second This, of course, is classic behavior that we saw from Big Tobacco. It was all about greed, it was all about marketing products. They didn't care about the resulting effect they were creating in their customers. In fact, the tobacco companies really only wanted to make sure their product didn't kill customers so fast that they lost a paying customer. They most likely didn't mind that it was giving them disease; they just wanted the customer to stay alive long enough to keep buying more product. To some degree, this mindset is still present in the pharmaceutical industry. You see this incredible insensitivity to the human condition in Big Pharma. You see press releases and memos from inside the pharmaceutical companies saying , "We can't wait for the Alzheimer's wave to come. We can sell a lot of drugs! Look at all those Alzheimer's patients out there!" Obviously I'm paraphrasing, but this is the kind of attitude we see. They look at diseases as opportunities, and that's sick! To look at a disease and how it's sweeping across the nation and affecting millions of people, and have dollar signs ringing up in your eyes and thinking, "Wow! This is great! We can make so much money selling drugs to all these people who are going to have Alzheimer's, or dementia, or osteoporosis." That's what goes on every single day in the back alleys of Big Pharma; or rather, I should say, in the executive office suites of Big Pharma. There are no back alleys; they're doing quite well financially. Exploiting the public for financial gain Whether it's Big Tobacco or Big Pharma, the similarities are very obvious at this point. It's all about making money, and selling a product to people. It's about exploiting the public for financial gain, while disregarding the true effects of your company's products on the public health. That, to me, is a crime. It's not just a crime in the legal sense, but in the spiritual sense, a crime against a fellow human being. To exploit their pain and suffering for your financial gain is unethical and immoral. It's bad karma and it should be against the law. Instead, many of these companies are actually propped up today. Business magazines talk about them as great successes, and their CEOs are named as some of the most successful business people in the country. They sit on various boards, and they're influential people. I ask myself, "What great good have these people accomplished?" Nothing! Where are the cures for any of these diseases? Where are all the cures? I haven't seen a single cure for any disease come out of the pharmaceutical industry since insulin came out. And that doesn't even cure diabetes, although it does regulate blood sugar. So where are the cures? Where is this big turnaround in health if everybody's taking so many drugs? If drugs are so good for everybody, shouldn't we be the healthiest population in the world? Where are those statistics? Well, they don't exist! We're the most diseased population in the world, the most diseased in the history of the world. We have never seen a population this diseased, and we're taking more drugs than anybody. We're spending the most money on healthcare. We're supposed to have the greatest healthcare system in the world, yet we're the sickest! We're the craziest in this country, too. We have more mental disorders, behavioral disorders, school violence -- we have people shooting their friends and classmates -- we have more people with dementia and Alzheimer's than we've ever seen before. So where are all these medicinal miracles? They're nowhere. The whole thing is a giant distortion and an illusion. Pharmaceuticals offer us nothing. It's just like nicotine and cigarettes. They offer us nothing other than a quick fix; nothing other than something to try to make us feel comfortable in the short term. Meanwhile, they are destroying our health from the inside out. In both cases, they're also destroying us economically. Class action lawsuits: the downfall of Big Pharma? The last similarity between these two companies is the class action lawsuits. Of course, Big Tobacco has fended off a lot of lawsuits. There was a Big Tobacco settlement a few years ago where the states got involved, and I think there is just such a lawsuit coming against the pharmaceutical companies. I think the pharmaceutical companies have dug their own grave. They have over-hyped, over-promoted, over-prescribed, over-pushed, and over-advertised all these prescription drugs. As a result, they now have over 40 percent of the population taking drugs. This means that as the facts start to come out about how these drugs are killing people and causing disease, and sometimes causing the very disorders they claim to treat, there's going to be a huge backlash -- a major class action lawsuit. Most of the adults in this country will probably be involved. We've got drugs out there that are extremely dangerous, even over-the-counter drugs like non-steroidal anti-inflammatory drugs, which, by the last study I saw, are killing 16,500 Americans per year just from gastro-intestinal bleeding alone. These are the numbers from one of the drug safety researchers at the FDA. That's just one drug, one over-the-counter drug, killing 16,500 a year. I think there's a big backlash coming, just like there was against Big Tobacco. Times are changing; people are realizing that pharmaceuticals are not safe, that they need to look beyond drugs. They need to look beyond these magic pill solutions and start taking responsibility for their own health. People are figuring out that if they go to the doctor and believe everything their doctor tells them, they'll most likely end up on one or more prescription drugs that will turn out to be unsafe years down the road, after the damage has been done. Most of these drugs are just giant experiments. And people are just guinea pigs to the drug companies. These drugs are not well tested. They're not in widespread use. All these trials have been carefully selected and constructed, but afterward they are distorted anyway. These are not safe drugs, but the drug companies know they can make enough money to fend off the lawsuits and even settle with patients, so they still come out ahead, even when their drugs literally kill people by the thousands. But that's the big trend coming -- massive nationwide lawsuits against the pharmaceutical companies with the states and the Attorney General getting involved. People like Eliot Spitzer, a fantastic champion of protecting the public and going after corrupt corporations will play a part. We've got states right now suing drug companies for all kinds of billing fraud. We're talking about hundreds of millions of dollars in fraud, in which these pharmaceutical companies would just over-bill states. I saw statistics in which some drug companies were billing states, I believe, $900 for a bottle of electrolyte solution for IVs. This should be about $20, and it's being billed at $900. It was a long list of items being overcharged. The states were shelling out this money to the pharmaceutical companies, being scammed one day after another, just like the American people are being scammed. I say the pharmaceutical industry is the greatest con ever perpetrated on the American people. It's a huge con, and they've got everybody behind it. They've got the FDA backing it up, they've got the doctors and the medical profession, and even the medical schools and the medical journals behind it. A lot of the mainstream media as well, because the drug companies spend so much money in advertising that they can pick up the phone and talk to the editors of these big magazines and news networks. They have influence because they spend the bucks. It's a huge con and it has far-reaching implications, and its roots are deep and widespread throughout society. It's going to be difficult to get rid of this, but times are changing. History will not judge Big Pharma kindly Some day, Big Pharma will be looked at in much the same way that Big Tobacco is looked at today. Today, Big Tobacco is not doing so well here in the United States. What has Big Tobacco done? They have turned to the international market. The American people finally figured out that cigarettes are a dangerous product and started passing laws about not selling cigarettes to minors, restricting the advertising of tobacco companies, and so on. But the tobacco companies figured out that they can exploit other countries. "Let's go sell cigarettes in China." Guess what, the smoking rate in China is skyrocketing. They're selling a whole lot of cigarettes over there, and killing a lot of Chinese people in the meantime. We're talking about Hong Kong, China, Taiwan, Japan, Thailand, North and South Korea, Malaysia, Singapore, Indonesia, and all throughout Southeast Asia. We have a huge smoking problem and it's the American cigarette companies that are over there exploiting those populations and literally poisoning and killing those people just to make a buck, because they figured out they couldn't make their money over here in the US anymore. The game was up. They got caught red handed here in the US. Eventually some of those other countries will figure it out too. Hopefully, we eventually won't have a tobacco industry in this country or anywhere in the world. That would be ideal. Hopefully, people don't need to inhale these deadly products. When the backlash happens against Big Pharma, we're going to see the same thing. Big Pharma here will finally have to get creative and try to sell their products overseas. They will very likely start exploiting Asia again. There's a whole lot of people over there, they need drugs too. They'll go over there and try to discredit traditional Chinese medicine, and they will try to discredit herbs and acupuncture, just like they've done here in the US. They will create a market where they force people to have only one option for treating diseases or symptoms: prescription drugs. The same scam worked here in the US. They convinced most people that drugs are the answer, even doctors, who are smart people. Why not try it in Asia as well? I'm sure they will. They're doing it already. They will just accelerate it as they become exposed here in the US, as people learn the truth about the dangers of prescription drugs. A few legitimate uses of drugs With all this talk about the pharmaceutical industry, you might say, "Mike, don't you have anything good to say about the pharmaceutical industry?" Yes, sure. It's great to have antibiotics if they're used properly, which they aren't. They're overused today. It's great to have anesthetics. If you need a surgical procedure because you've been in a car crash or you've experienced some kind of physical trauma or injury, you need anesthetics. You need antibiotics during that surgery. You need this technology to help put you back together physically. Traditional, organized Western medicine has a place. I don't deny that. Even prescription drugs can have a place if used temporarily, only for short term treatment of acute symptoms and acute conditions, and only when paired with education and lifestyle changes that can help that patient eliminate the very causes of the conditions that created that disease in the first place. The pharmaceutical industry does have a place; but frankly, it's only justified role in society is maybe something like one-twentieth of its current size. We don't need 40 percent of the population taking pharmaceuticals at any one time, we only need about 2 percent. The other 38 percent should be on nutritional healing programs. They should be on lifestyle changes, strength training, physical exercise, exposure to natural sunlight, and consumption of fresh water on a more regular basis. They also need healing foods and healing therapies. They don't need drugs. Where is the shame of doctors? Doctors will some day look back on this and they will be embarrassed that they supported prescription drugs for so long. They will be embarrassed in the same way as they are today about the truth that they promoted cigarettes. No doctor is proud of being associated with a profession and with an American Medical Association that has actually promoted these things in the past. The American Medical Association has even been convicted twice in the federal courts of conspiracy, for conspiracy to discredit chiropractic medicine. This is a history that doctors shouldn't be proud of. Perhaps a lot of them don't even know this history, but this is the real history of medical doctors in this country. In the future they will look back to today and say, "We are ashamed that we promoted all of these drugs, that we prescribed them without teaching patients how to be healthy. We are ashamed of our profession, and it's time to make some changes." They indeed should be ashamed, because right now old school medical doctors are doing tremendous harm. The first rule of medicine: Do no harm. That has been forgotten, because every time a doctor sees a patient, spends three minutes with that patient, writes a prescription, and sends them out the door to go to the pharmacy, that's doing harm. That is irresponsible medicine. In fact, it is not even healing at all. It's not even being a doctor. The word "doctor" means "teacher", according to the Latin root. Where is the teaching in our doctors today? It's not present, except in the really great doctors. But by and large, the run-of-the-mill general practitioners are not teaching anybody anything. They're writing prescriptions and getting them out of the office. Some say, "We don't have time to teach people." Then, what are you doing? What are you doing as a doctor? What are you doing in this profession if you don't have time to help people? Didn't you get into medicine because you wanted to help people? Stop wasting your time being a slave of the drug companies. You will be embarrassed about that some day, believe me; instead, go study naturopathy. Go learn nutrition ( see related ebook on nutrition). Go help people in meaningful ways. Don't be part of the machine that is causing pain, suffering, destruction, and death in our society and around the world right now. That machine is set up for one purpose, which is financial profit. Refuse to be part of that machine. Just say no to prescription drugs For the rest of us, we can cause the vanishing of both Big Tobacco and Big Pharma by simply not purchasing their products. We can go somewhere else, we can do something different. We can use homeopathic remedies or acupuncture to treat our acute systems. We can use nutritional healing and lifestyle changes to prevent chronic disease so that we don't become a patient in the first place. We won't suffer from Alzheimer's and dementia and these so called "aging diseases," which really have almost nothing to do with aging; but modern medicine loves to describe it that way to try to make you think it's inevitable. We can make these changes. We don't have to be a customer of organized medicine. We can say "No" to cigarettes; we can say "No" to prescription drugs. We can find alternatives. I encourage you to take responsibility for your own health, to seek out those alternatives and use them. Don't be a victim. Don't be exploited by tobacco companies or pharmaceutical companies just so that you can make their CEOs rich at your expense. | |
Posted by PurpleIvy, 17:44 26 March 2007I will not subscribe to the view that we should all say NO to prescription drugs. My husband has to take daily medication otherwise he could not live a normal life.
I do not believe that nutrition and lifestyle changes would remove his condition. I haven't heard of anyone treating it like that. He has taken the prescription drug for his condition since 1981 and is appropriately monitored by his GP. Stopping his medication would mean that the condition he has would not be under control. Perhaps the GPs in our local practice are out of the ordinary, but they do not prescribe antibiotics as frequently as the author of the above seems to think. Medication of may types improve the quality of life for so many people. In some cases they make it bearable. A blanket statement that we all ought to avoid all medication at all cost seems a bit too extreme to me. In modern life people take risks. OK, in some cases taking a drug is a risk, smoking is a risk , as is drinking alcohol. Eating certain foods may deemed to be risky, stepping into my local high street, getting on a train or bus or plane may be risky, as is driving a car. But they are all deemed to be acceptable risks to take in modern life. Some choose not to drink or smoke, few stay at home because it is dangerous to go out and some take bigger risks and participate in extreme sports and activities. We assess the level of risk we are prepared to take. My husband and I both take prescription medicines for different reasons, because we value our quality of life. The risk is so small as to seem piffling compared with some of those listed above. Whenever you take medication, either prescription or OTC you have to decide if you want to put up with side effects and/or risks or whether you'd rather just cope with the condition. I think you need to spend a little time getting things into perspective Linda and to look forward to the rest of your life, rather than focussing so strongly on what has already happened. Of course the Pharmaceutical companies are out to make money, they're businesses and that's what businesses do. You don't have to take drugs if you don't want to, just accept that the Pharmaceutical companies aren't out to 'get you' and that they help a lot of people. | |
Posted by Linda, 17:57 26 March 2007The article doesn't say that all prescription meds are bad. It says that many of them would be unnecessary if appropriate changes are made in the person's life. Not all of them, but most. I know that most people dismiss the idea of nutritional healing as nonsense. I've seen it work for many people firsthand, but that's a whole other topic and I don't want to get into any more arguments.
I actually came here just now to say that I've put a lot into this topic and I'm particularly happy with the previous article as a way to end it for a while. People can find their way here if they are interested; I want to allow this topic to find its way off the first page and let arguments die down. I want to inform, not provoke. It's fine by me if people come here to disagree. I think the info here speaks for itself and some may find it useful. I needed to know these things myself before I took my med. Best wishes to all for a life full of health, spirituality and vibrance. Linda. | |
Posted by Linda, 10:08 30 April 2007Role of antidepressants in killings needs review
http://www.modbee.com/local/story/13533556p-14137410c.html http://www.modbee.com/local/v-dp_morning/story/13533556p-14137410c.html The Modesto Bee Role of antidepressants in killings needs review By TY PHILLIPS April 29, 2007 The murderous rampage that left 33 people dead at Virginia Tech has stirred countless emotions: sadness and anger, fear and hatred, grief and disgust. When Dr. Ann Blake Tracy heard the details, she felt many of those same emotions. Yet there is one sentiment Tracy does not share with much of the rest of the world: surprise. As terrible as it sounds, after nearly 20 years researching links between violent crime, suicide and antidepressants, Tracy is surprised only that it doesn't happen more often. Details continue to emerge about the lonely life of killer Seung-Hui Cho, who had a history of mental illness. Among Cho's effects, officials found prescription medications related to the treatment of psychological problems. Though it's still premature to draw conclusions without toxicology results, these are the details Tracy, an author and the executive director of the International Coalition for Drug Awareness, expected from the moment she heard about the Virginia Tech shootings. In her experience, when it comes to investigating high-profile shootings, antidepressants are as common as the presence of loneliness, despondence and rage. "I'm just so tired of seeing people die, I could scream," Tracy said during a phone interview. "It's happening daily in this country. It's so massive, it's just unreal. We've got so many school shootings now, I can't even begin to keep up with them all. And the reason is so incredibly obvious. You don't have to look at much to figure it out." 2006, Bailey, Colo. - Duane Morrison shot and killed a girl and sexually assaulted six others. Antidepressants were found in his vehicle. 2005, Red Lake Indian Reservation, Minn. - Jeff Weise shot and killed nine people and wounded five before committing suicide. Prozac. 1998, Springfield, Ore. - Kip Kinkel killed his parents, then went to school and opened fire in the cafeteria, killing two and wounding 22. Prozac. 1989, Stockton - Patrick Purdy used an assault rifle to spray bullets through a playground at Cleveland Elementary School, killing five children and wounding 29 people before he killed himself. Elavil. 'It's all so intertwined' There are dozens of other examples of violence at schools and the presence of antidepressants, but the carnage hardly is limited to our campuses. Countless families have been destroyed around the world through homicides and suicides committed by adults on antidepressants. In June 2001, Texan Andrea Yates drowned her five children under the influence of four psychiatric medicines, including Effexor. In February 2004 in Polk Township, Pa., Samantha Hirt, hours after taking a pill for manic depression, set fire in a bedroom where her two toddlers were playing, closed the door and sat on a sofa watching television while the fire spread, killing both children. Effexor. Other famous cases include the 1998 deaths of actor Phil Hartman and his wife, a murder/suicide committed by her (Zoloft); the 1999 home and office killing spree by Atlanta day trader Mark Barton (Prozac); the 1998 shooting deaths of four co-workers by Connecticut lottery accountant Matthew Beck, who then killed himself (Luvox); and the 1994 New York City subway bombing by Edward Leary, which injured 48 (Prozac). The list (which can be found at <http://www.drugawareness.org/> www.drugawareness.org) encompasses hundreds and hundreds of cases. "You start linking them together and looking at all the similarities and you say, 'Good grief, it's all so intertwined,'" said Tracy, who has appeared on programs including "20/20," "Dateline" and "60 Minutes" and served as a consultant on high-profile cases including Columbine and Andrea Yates. "I keep asking, 'When is somebody going to see this?' But we've been so brainwashed about drugs, we think legal means safe. "Most people don't know LSD once was prescribed as a wonder drug. Most people don't know that PCP was considered to have a large margin of safety in humans. Most people don't know ecstasy was prescribed and sold for five years to treat depression. Few know that history of drugs, and I think that's our biggest problem. We're just not educated enough to have concerns." Prozac nation, indeed The Northern San Joaquin Valley certainly is not immune. Stanislaus County Coroner Kristi Herr, who has investigated hundreds of the county's 4,000 annual deaths, including many accidental overdoses of prescription medicines, said she regularly goes into homes of deceased people and finds medicine cabinets loaded with prescription medicines. Sometimes there are so many pill bottles that large garbage bags are needed to transport them all. "It seems to me a large portion of our society is on antidepressants," Herr said. "That isn't based on statistics. That is just based on my experience of going into homes and evaluating the cases that come through here." In 2003, then-Newman resident Lorraine Slater's 14-year-old daughter, Dominique, killed herself after being treated for depression with several antidepressants, including Celexa and Wellbutrin. As her depression and erratic behavior worsened, her doctor prescribed her a double dose of Effexor. Fifteen days later, she was dead. Her body later was found in the Delta Mendota Canal in Patterson, not far from the family's home. "On the drug, she became more agitated, combative and restless," Slater said. "And she had never been like that before. It's like our daughter was on LSD. It was a real Dr. Jekyll and Mr. Hyde experience." Shortly after Dominique's death, the FDA released a warning that one in 50 patients, or 2 percent, will experience an adverse reaction to Effexor, which can include suicidal thoughts. Slater has become a consumer advocate working to raise awareness of possible dangers of antidepressants. On May 9, she will testify at a hearing at the state Capitol concerning a bill that would require drug companies to disclose results of all clinical trials. "We're not against medication," Slater said. "We just want disclosure about results from their trials. In their internal memos, marketers are told to downplay the side effects, and a lot of doctors aren't aware of the real dangers. "We're just saying these companies need to give the citizens they're supposedly trying to help the information about possible symptoms so people can make informed decisions. If their medicine is so good, what is there they have to hide?" Arguments against link Of course, the logical argument against tying violent crimes to antidepressants is that there are countless factors that motivate a person to commit a violent act. And those who carry out these deeds often are people with mental illness, so the presence of antidepressants can be expected. These are solid points; correlation does not in itself mean causation. And there is no doubting that countless people have benefited from these drugs. Still, as one looks at the details of violent crimes around the country, too often there is an array of antidepressants. At the very least, this is a topic that deserves greater scrutiny. In early 2005, the FDA issued a warning that antidepressants can cause both suicide and violence. The agency also mandated a black-box warning - the most serious available - that states these drugs can produce side effects that include anxiety, agitation, panic attacks, irritability, hostility, aggressiveness, impulsivity and mania. The FDA also has warned that abrupt withdrawal of antidepressants can produce suicide, psychosis or hostility. Eli Lilly, which makes Prozac, repeatedly has denied claims that Prozac causes violence, even though the company's own documents acknowledge "nervousness, anxiety, self-mutilation and manic behavior" are among the "usual adverse effects" of the medicine. It's the same Eli Lilly that has paid more than $1.2 billion to 28,000 people who claimed they were injured by the drug Zyprexa during the past decade, according to a Jan. 5 article in the New York Times. Paying $1.2 billion over 10 years may sound like a lot of money until compared with the $4.2 billion the company made last year alone selling Zyprexa, which has been taken by 20 million people worldwide since its introduction in 1996. Most antidepressant drugs, including Prozac, Zoloft, Paxil, Luvox, Celexa, Lexapro and Effexor, are known as selective serotonin reuptake inhibitors, which alter brain chemistry in an attempt to manage depression. Serotonin, a neurotransmitter, is a chemical that facilitates communication within the brain, allowing one to experience happy feelings upon its release. Essentially, the antidepressant drugs prevent reabsorption of serotonin in an attempt to make the happiness experience last longer. Mother of a monster One of the former lead chemists at the National Institute of Health, whose work eventually led to the development of many antidepressant drugs, first spoke out against the drugs nearly 10 years ago. "I am alarmed at the monster that Johns Hopkins neuroscientist Solomon Snyder and I created when we discovered the simple binding assay for drug receptors 25 years ago," said Dr. Candace Pert in the Oct. 20, 1997, issue of Time magazine. She said Prozac and other SSRI (selective serotonin reuptake inhibitor) antidepressants may cause heart problems and affect the entire body, where the vast majority of serotonin is produced. The medical profession "ignores the body as if it exists merely to carry the head around," said Pert, who's now scientific director of RAPID Pharmaceuticals in Potomac, Md. "These molecules of emotion regulate every aspect of our physiology." A recent study by the Centers for Disease Control and Prevention found that half of all Americans take at least one prescription drug, and that antidepressant use has nearly tripled in the past decade. According to some estimates, 30 million Americans take antidepressants. FDA statistics show U.S. physicians issue more than 10 million antidepressant prescriptions each year to patients younger than 18. FDA-approved prescription drugs injure 2.2 million and kill at least 100,000 Americans each year, according to numerous published studies. Some survive and forgive Problem is, when antidepressants don't work as intended, the harmful fallout isn't limited to the user. The victims often are those within striking distance. They are people like Mark Taylor, who was sitting outside and reading a Bible when he was shot numerous times by Eric Harris at Columbine High School. "The first one hit me in the back of the leg. That was the shotgun blast," Taylor said in a recent phone interview. "That was the most painful. And then I got hit several more times in the chest; the bullets went right through me. They tried to make sure I was dead. I laid down and pretended I was dead. "I think Eric Harris, from the medication, didn't really know what he was doing. I don't really hold him responsible for it. Eric and Dylan were both taking medicines. They just didn't seem to have any reaction to what they were doing. They were having fun with it, laughing and enjoying it and having a good time. I feel that antidepressants were the cause of the Columbine shooting." Taylor, now 24, travels the country and speaks about the importance of forgiveness. Since the Virginia Tech shootings, he has been besieged with interview requests. His interviews included an appearance on "The Morning Show with Mike and Juliet," a national Fox News Network program. The hosts invited Taylor because they wanted to hear from someone who had survived a school shooting, someone who presumably could offer insight to help other children survive such an incident. "Forgiveness," Taylor told them, "that's how I survived it." But Taylor said the show's commentators weren't much interested in his message of forgiveness. Instead, the show focused on interviews with FBI agents and police tacticians, who offered survival tips that we are supposed to use to arm our children as we send them off to school. Is this what it's come to? Do we now simply accept that frequent school shootings are a part of today's society and prepare ourselves for when tragedy strikes? Too often, instead of working to find the cause of problems, we react to symptoms. That same kind of thinking is what has so many Americans taking antidepressants in the first place. | |
Posted by Linda, 10:19 30 April 2007Debunking biological psychiatry
Dr. Wayne Goodman - FDA announcement: ALLIANCE FOR HUMAN RESEARCH PROTECTION (AHRP) Promoting Openness, Full Disclosure, and Accountability http:h//www.ahrp.org/cms/ FYI "Biological psychiatrists have looked very closely for a serotonin imbalance or dysfunction in patients with depression or obsessive compulsive disorder and, to date, it has been elusive," says Dr. Wayne Goodman, Chair of the US Food and Drug Administration (FDA) Psychopharmacologic Drugs Advisory Committee. Psychiatry's drug prescribing practices rest on a myth debunked by Jeffrey Lacasse and Jonathan Leo in their article in PLoS Medicine. Not a single representative of mainstream psychiatry has come forward to rebut them. Lacasse and Leo lay out the case against psychiatry's bedrock justification for prescribing psychotropic drugs. For decades psychiatry's leadership and chorus of followers have claimed that depression is caused by a "chemical imbalance" in the brain, and that SSRI antidepressants normalize that "chemical imbalance." But such claims have been overturned In the absence of evidence. As Lacasse and Leo have shown, not a single peer reviewed article validates the theory of a chemical or biological marker abnormality in persons diagnosed with depression--or, for that matter with any psychiatric disorder. Thus, neurologist, Dr. Frederick Baughman argues, in the absence of a confirmed disease, no medical intervention is justified. Evidence does exist showing that the drugs have serious adverse effects which, for some individuals, cause permanent damage. Furthermore, some of the prescribed drugs are controlled class II substances--which means they are highly addictive! We are led to ask: What is the justification for giving psychiatrists a license to prescribe psychotropic drugs in the absence of evidence that: 1. A pathological abnormality is present; 2. The prescribed intervention (drug) is proven safe; 3. The intervention is proven effective to treat the pathology; 4. The benefit / risk ratio is favorable for those for whom it is prescribed. See: Jeffrey R. Lacasse, Jonathan Leo. Serotonin and Depression: A Disconnect between the Advertisements and the Scientific Literature, PLoS Medicine, Dec 2005 at: http://medicine.plosjournals.org/perlserv/?request=get-document&doi=10.1371/jour\ nal.pmed.0020392 See also: http://www.ahrp.org/cms/content/view/67/94/ Contact: Vera Hassner Sharav 212-595-8974 veracare@... | |
Posted by Linda, 10:20 30 April 2007Depression and Mood Disorders
Feelings of hopelessness, chronic apathy, and low energy levels are some of the crippling symptoms of depression. Depression can appear as a consequence of a life change such as divorce, death of a family member, or loss of work. The well-known adage, "sound body-sound mind" reveals a simple basic truth. That's because depression is commonly intertwined with a vast number of diverse conditions and illnesses--and uncovering potential imbalances can be a powerful tool for an effective natural and holistic approach to emotional healing. Depression and Amino Acids: The building blocks of protein, amino acids are crucial source material for the production of important brain neurotransmitters. Imbalances can result in several major dysfunctions of the central nervous system linked to depression. Depression and Thyroid Function: A substantial portion of patients with depression suffer from thyroid hormone imbalances that may make them more treatment-resistant. Depression and Allergy: Depression seems to predispose individuals to increased immune hypersensitivity to a wide range of food and environmental allergens. Depression and Melatonin: Imbalances of the pineal hormone melatonin are linked to Seasonal Affective Disorder and other mood and behavior problems. Disrupted secretion patterns of melatonin can also seriously interfere with sleep, worsening existing symptoms of depression. Depression and Adrenal Hormones: Overly high levels of the adrenal hormone cortisol often underlie the biochemical pattern characteristic of depression, particularly when stress and obesity are also part of the clinical picture. Depression and Digestive Function: A faulty digestive process can result in the malabsorption of key nutrients necessary for maintaining healthy mood patterns and overall feelings of well-being. Overgrowth of certain intestinal yeasts such as candida albicans can also trigger mood swings. Depression and Toxins and Nutrients: Overexposure to heavy metal toxins like lead and mercury have been clinically shown to induce a psychiatric symptoms such as anxiety and depression. Mineral nutrient imbalances can also cause resistance to treatment. Depression and Glucose and Insulin Tolerance: Fluctuating blood sugar levels, particularly in diabetic patients, can result in increased depression, tension, and fatigue. Depression and Vitamins: The B-vitamins play an important role in the proper metabolism of important brain neurotransmitters linked to mood and behaviour. Depression and Fatty Acids: Fatty acid deficiencies could significantly contribute to symptoms of depression, particularly in those at high risk of omega-3 deficiencies, such as alcoholics and post partum women. Depression and Female Hormones: Female hormone imbalances may help explain why women are much more prone to certain types of depression than men. | |
Posted by Linda, 10:21 30 April 2007Jefferson Scientists Show Several Serotonin-Boosting Drugs Cause Changes in Some
Brain Cells Some cells shriveled, while others took on corkscrew shapes Researchers from Jefferson Medical College in Philadelphia have found changes in brain cells in rats treated with large doses of several anti-depressant or anti-obesity drugs. In some cases, the cells shriveled or took on abnormal corkscrew shapes. While the clinical significance of the findings isn’t known, the scientists say, they may raise new concerns about the prolonged use of such commonly prescribed drugs as fluoxetine (Prozac) and sertraline (Zoloft). The work also highlights the need for similar studies on other classes of drugs that act on the central nervous system. The scientists, led by Madhu Kalia, M.D., Ph.D., M.B.A., professor of biochemistry, molecular pharmacology, anesthesiology, and neurosurgery at Jefferson Medical College of Thomas Jefferson University in Philadelphia, compared the effects of giving high doses for four days of four drugs – Prozac, Zoloft, sibutramine (Meridia) and dexfenfluramine (Redux) – on rat brain cells. Each rat received only one drug. In the study, after the toxic doses of drugs were halted, and the animals’ brains subsequently examined, the researchers saw marked changes in some nerve terminals, which actively release the brain chemical serotonin. These drugs, collectively known as Selective Serotonin Reuptake Inhibitors (SSRIs), increase the level of serotonin, which is vital to brain cell communication. Low serotonin levels are linked to mood and eating disorders. Dr. Kalia and her colleagues at Jefferson and at the Centers for Disease Control and Prevention and the National Institute of Occupational Safety and Health in Morgantown, WVa., report their results March 6 in the journal Brain Research. The question remains, what do these findings mean. "We don’t know if results with four days of drug treatment are clinically significant," Dr. Kalia says. "We don’t know if the cells are dying. That’s the key question. We need to do more studies to prove cell death. These effects may be transient and reversible. Or they may be permanent." Prozac and Zoloft are Food and Drug Administration-approved medications for the treatment of depression and other central nervous system disorders. Meridia is marketed for the treatment of obesity. The anti-obesity drug Redux was pulled from the market in 1997 after reports of heart valve damage. Methylenedioxymethamphetamine (MDMA), known as the street drug Ecstasy, is an amphetamine-derivative that is known to be toxic to some brain cells. MDMA and another drug, 5,7-dihydroxytryptamine (5,7-DHT), were used as controls because both drugs push serotonin out of the brain cells. The brain cell changes with SSRIs were similar to those observed with MDMA. Serotonin is ubiquitous in the central nervous system, making it a frequent target of potential drugs. Drugs such as Prozac and Zoloft raise serotonin levels for depression and panic attacks, for example. Another class of SSRIs – anti-anorectics – includes drugs such as Meridia and its predecessor, Redux. Such drugs block the circulating serotonin, a neurotransmitter. Once brain cells use serotonin, it’s recycled in the brain. SSRIs keep serotonin from being recirculated back to the brain for subsequent use, allowing the chemical to stay active in the brain. More than a decade ago, rat studies showed that high doses of Redux could change the shape of some brain terminals, says Dr. Kalia. Some researchers attributed the effect to the fact that the drug was also a serotonin releaser. It pumps extra serotonin out of the brain cell, depleting the brain cell nerve terminal, rather than just blocking serotonin from entering back into the cell. "It was a big mystery why these brain terminals looked like corkscrews with high doses," Dr. Kalia remembers. But, she says, few scientists examined all SSRIs. "We asked the question, ‘Would other SSRI’s cause the same effects in high doses’?" Because patients are using some of these drugs for long periods – and scientists aren’t sure of what the long-term effects of many of these drugs might be – she and her co-workers plan to do long-term studies in animals. "We would lower the doses to about 10 to 30 times the therapeutic dose and give it to the rats for six months or a year, looking at them at selected periods of time to ask the questions, ‘Can we see these changes in serotonin cells over the long term, or does the brain adjust?’" she says. The scientists would then examine the long-term effects of the drugs and examine the behavioral and neurological effects of these brain changes. "We need to find out if these changes are effecting behavioral changes in the rat and in patients. "The problems with human studies is we can't do such experiments in controlled environment," she explains. One difficulty with using such drugs, she says, is that several of them are given to patients who already have psychological problems such as depression and mood swings. They may or may not develop neurological problems following drug treatment. Though that isn’t necessarily the case with patients taking anti-obesity drugs, she points out, in any case, "the possibility of overlooking any drug-induced neurological changes must be considered." Published: 2-29-2000 | |
Posted by Linda, 10:22 30 April 2007Prozac petition
To: The Office of the Surgeon General of the United States; The Department of Health & Human Services; The Federal Bureau of Investigations and The Justice Department We, the Undersigned, demand a Grand Jury Investigation into serious misconduct concerning Prozac on the part of Eli Lilly, the drug’s manufacturer. Specifically, we assert that Eli Lilly has known of and engaged in the suppression of the truth concerning the drug’s ability to cause suicide and suicidal ideation. We assert that Eli Lilly has knowingly and fraudulently concealed facts surrounding its drug’s deadly side effects. Documented findings of cover-ups supporting our demand include, but are not limited to, the following: · Eli Lilly has known Prozac (fluoxetine) causes akathisia, defined as an extreme subjective feeling of inner restlessness. This condition has long been known to be caused by antipsychotic drugs and recognized as leading to suicidal and homicidal-suicidal feelings. Lilly's own internal documents show the condition was identified in association with Prozac as early as 1978. · August 2, 1978, when only three trials were underway, minutes of a meeting of the Fluoxetine (Prozac) Project Team read: "There have been a fairly large number of reports of adverse reactions... Another depressed patient developed psychosis... Akathisia and restlessness were reported in some patients." A similar meeting held 10 days earlier stated, "…some patients have converted from severe depression to agitation within a few days; in one case the agitation was marked and the patient had to be taken off drug." The minutes further state, "…in future studies the use of benzodiazepines to control the agitation will be permitted.” From that point on, Lilly's trial subjects were put on tranquillizers to get them over the akathisia experienced by some in the early days on the drug. Those who developed akathisia or who had any suicidal tendencies were excluded from the trial data on the basis that they would otherwise obscure the results of the drug's success in treating depression. · Lilly internal documents, May 25, 1984 – Upon examing Prozac trial results, the German licensing authority (the Bundes Gesundheit Amt (BGA)) issued a letter stating: "During the treatment with the preparation , 16 suicide attempts were made, two of these with success. As patients with a risk of suicide were excluded from the studies, it is probable that this high proportion can be attributed to an action of the preparation ." · January 1985, the Germans told Lilly that they would not license the drug, citing "suicidal risk" as one of the reasons for their decision. Lilly's scientists continued trying to persuade the BGA to grant a license, but focused most of their efforts on the US. By August 1989, it was clear to Lilly that the BGA would demand that Prozac carry a warning to General Practitioners (GPs) that they should be aware of the risk of suicide unless they gave patients sedation along with Prozac. A warning of a "risk of suicide" finally went on the German package insert in 1992. It also stated, "For his/her own safety, the patient must be sufficiently observed, until the antidepressive effect of Fluctin sets in. Taking an additional sedative may be necessary." · During the licensing process in the US Lilly did not tell the FDA of the German concerns. · Lilly has repeatedly attempted to suggest suicidality reflects patient’s disorders. Yet, Lilly’s own scientist, John Heiligenstein, wrote in an internal memo on September 14, 1990: "We feel caution should be exercised in a statement that 'suicidality and hostile acts in patients taking Prozac reflect the patient's disorder and not a causal relationship to Prozac'. Post-marketing reports are increasingly fuzzy and we have assigned, 'Yes, reasonably related', on several reports. · This Heiligenstein memo was written two years after Prozac was granted a license by the FDA, and just months after a study report by Martin Teicher, Jonathan Cole and Carol Glod was published. According to the study, 6 patients with a history of depression became violently suicidal in a way that surprised themselves and their doctors while on the drug. The report noted that suicidal thoughts occurred within days or weeks of going on Prozac, or of having the dosage increased beyond a certain level, and that such thoughts disappeared when the patient stopped taking the drug. Lilly insisted that Prozac did not cause akathesia; the company asserted that the link between akathesia and suicide is questionable. · Lilly's internal documents of that time show that public criticism was threatening the drug’s success. Some were coming out of the UK. · An internal memo from Leigh Thompson, one of Lilly’s chief scientists, stated, "Anything that happens in the UK can threaten this drug in the US and worldwide…" "We are now expending enormous efforts fending off attacks because of 1) relationship to murder and 2) inducing suicidal ideation .” · Another memo from Thompson ran: "I am concerned about reports I get re UK attitude toward Prozac safety. Leber suggested a few minutes ago we use CSM database to compare Prozac aggression and suicidal ideation with other antidepressants in the UK. Although he is a fan of Prozac and believes a lot of this is garbage, he is clearly a political creature and will have to respond to pressures. I hope Patrick realizes that Lilly can go down the tubes if we lose Prozac, and just one event in the UK can cost us that.” (All points outlined above are supported by documented findings published in The Guardian; “They said it was safe”; Sarah Boseley; October 30, 1999) FURTHER SUPPORTING EVIDENCE: 1.As cited above, In 1990, Martin Teicher et al, of Harvard Medical School, reported six cases of "intense suicidal preoccupation" in patients who had been prescribed the drug. According to the authors, "none of these patients had ever experienced a similar state during treatment with any other psychotropic drug." (American Journal of Psychiatry, February 1990) 2. Dr. David Graham, chief of the FDA's Epidemiology Branch, wrote on Sept. 11, 1990, that Lilly's data on suicide and Prozac, and data garnered from a study by Drs. Maurizio Fava and Jerrold Rosenbaum of Massachusetts General Hospital (citing no significant difference in "suicidal ideation" in patients treated with fluoxetine compared to those receiving other antidepressants) was insufficient to prove that Prozac was safe. In an internal FDA memo, Graham wrote: "Because of apparent large-scale underreporting, the firm's analysis cannot be considered as proving that fluoxetine and violent behavior are unrelated." Rosenbaum's objectivity has been questioned. Not only was his study on Prozac and suicide criticized by at least two sets of researchers as well as the FDA, but also documents obtained by The Boston Globe illustrate Rosenbaum's questionable relationship to Lilly. He has served as a Prozac researcher and sat on a marketing advisory panel for Lilly before Prozac was launched. (Leah R. Garnett; “As drug gets remade, concerns about suicides surface”; Boston Globe, 5/7/2000) 3. In September 1991, an advisory committee of the FDA cleared Prozac. “Suicidal ideation" and "violent behaviours" were added to the label as "reported, but not proven." (Robert Bourguignon MD; “Problems with Prozac”; http://www.camtech.net.au/malam/reports/prozac.htm) 4. In 1994, David Healy (then consultant to Eli Lilly) published an article entitled "The Fluoxetine and Suicide Controversy, a Review of the Evidence” in which he stated that antidepressants, Prozac included, can indeed induce suicidal behaviour. (CNS Drugs, March 1994) 5. The FDA's adverse event reporting system (AERS) reveals 28,623 Prozac adverse events (ADEs) (Garnered from data gathered via Freedom of Information Act): · 63% of 1,734 deaths reported - 1,089 - were attributed to suicides. · Suicide attempts numbered 1,885. · Over 10% of the total 28,623 ADEs reported were attributed to suicides and suicide attempts. 6. By the Government Accounting Office’s own admissions, reported FDA Adverse Drug Events only reflect an estimated 1%, to a conservative 10% of actual events, and “are unlikely to be representative of the much larger number of unreported events.” (“Adverse Drug Events – the Magnitude of Health Risk is Uncertain Because of Limited Incidence Date”, Jan. 2000; GAO/HEHS-00-21) Given this lack of actual data, Prozac numbers could be projected to be in the area of 10,890 deaths by suicide and 18,850 suicide attempts at 10% reporting. At 1% reporting, 108,900 suicides and 188,500 suicide attempts could be projected. 7. Recent studies reveal over 50,000 deaths related to Prozac and estimate that between 7% and 10% of individuals exposed to Prozac will have some kind of adverse reaction. (The Boston Globe; "As drug gets remade, concerns about suicides surface"; Leah R. Garnett, Globe Staff; May 7, 2000; © Copyright 2000 Globe Newspaper Company) 8. According to internal documents and other documented material made available to The Boston Globe, (Leah R. Garnett, Globe Staff; “As drug gets remade, concerns about suicides surface”; The Boston Globe, 5/7/2000): · In 1990, Lilly scientists were pressured by corporate executives to alter records on physician experiences with Prozac, changing mentions of suicide attempts to "overdose" and suicidal thoughts to "depression." In an electronic communiqué (obtained by author Dr. Joseph Glenmullen, Prozac Backlash) from Claude Bouchy, a Lilly employee in Germany, to three Lilly corporate executives at Lilly’s Indianapolis headquarters, dated November 13, 1990: Bouchy says he and a colleague "have problems with the directions our safety people are getting from the corporate group (Drug Epidemiology Unit) and requesting that we change the identification of events as they are reported by the physicians. . ." He further reported, “Our safety staff is requested to change the event term `suicide attempt' to `overdose.' " He added, “...it is requested that we change . . . `suicidal ideation' to `depression.' " He informed his US Lilly colleagues: "I do not think I could explain to the BGA, to a judge, to a reporter or even to my family why we would do this especially on the sensitive issue of suicide and suicidal ideation. At least not with the explanations that have been given to our staff so far." · Three years before Prozac received approval by the US Food and Drug Administration in late 1987, the German BGA had such serious reservations about Prozac's safety that it refused to approve the antidepressant based on Lilly's studies showing that previously non-suicidal patients who took the drug had a fivefold higher rate of suicides and suicide attempts than those on older antidepressants, and a threefold higher rate than those taking placebos. · Lilly's own figures indicate that 1 in 100 previously non-suicidal patients who took the drug in early clinical trials developed a severe form of anxiety and agitation called akathisia, causing them to attempt or commit suicide during the studies. · A patent for a new Prozac (US Patent no. 5,708,035), R-fluoxetine, expected to be marketed by Lilly beginning in 2002, (as of the 2000 Globe report) states the new version will not produce several existing side effects including "akathisia, suicidal thoughts, and self-mutilation…one of its more significant side effects." This is the same effect Lilly has repeatedly denied to have occurred in any substantial way in some 200 lawsuits against them over the past decade. Most of the suits were settled out of court and the terms kept confidential. · Lilly will pay Sepracor, Inc., who holds the patent for the new Prozac, an upfront payment and license fee of $20 million and an additional $70 million based on the progression of the drug. Lilly will have exclusive world rights to the drug, will be responsible for development, product manufacturing, regulatory submissions, and marketing and sales – Sepracor to receive royalties according to a Sepracor press release dated April 13. · Dr. Martin Teicher, whose early 1990’s studies linked Prozac to akathisia and suicide, is a co-inventor of the new Prozac, along with Timothy J. Barberich, the CEO of Sepracor Inc., (a Marlborough drug company), and James W. Young. They filed their patent in August 1993, the same year Teicher published "Antidepressant Drugs and the Emergence of Suicidal Tendencies”, which concluded that patients on Prozac were at least three times more likely to become suicidal than those on older antidepressants. (Journal Drug Safety) · Figures in a 1984 Lilly document indicated that akathisia, the severe agitation that can lead to suicide, occurs in at least 1 percent of patients, a level considered a "frequent" event, and as such must be disclosed in a company's product literature and package inserts. But there is no such disclosure in Prozac's US literature. Akathisia is listed in Lilly's US product literature, but as an infrequent event in Prozac users. No mention is made of its potential relationship to suicide. In conclusion, we believe the FDA and Eli Lilly must be held accountable as to their negligent, fraudulent and cover-up activities concerning this deadly drug. Given the above cited findings, we firmly believe that it is only through a Grand Jury Investigation that the rights of the unsuspecting American consuming public can be best served, that unconscionable future suffering may be averted, and many lives saved. We, the undersigned, most earnestly request that a thorough investigation into Eli Lilly’s and the FDA’s practices concerning Prozac, both past and present, be vigorously pursued as per the powers vested in you to do so. Countless innocent lives depend on it… “All truth passes through three stages: First it is Ridiculed. Second, it is Violently Opposed. Third, it is Accepted as being Self-Evident.” - Arthur Schopenhauer (1778-1860) Respectfully Yours, Sincerely, The Undersigned Petition Signature Number: 9,950 Edwin S. Purcell, Ph.D. As a Neuroscientist, I implore you to heed this petition. -------------------------------------------------------------------------------- http://www.petitiononline.com/lilpro/petition.html Currently 17,688 Total Signatures ( as of April 8, 2007) -------------------------------------------------------------------------------- 17512. Dr. Ken Weil Atlanta GA 17390. Lisa Loring RN these drugs do more harm than good, DOC remember that OATH!? 17350. Dr. Glen R. Burford 17247. De Lyn Wolcott, CPhT Lubbock, TX USA 16136. Dr. Jarrod A. Fancher 111 West Vine St., Keller, TX 76248 USA 15437. Dr. Michael C. Mulvaney 15376. Dr. jennifer zipfel As a doctor, I have seen alot of negative side effects with Prozac in their behavior and reactions to other meds. 15189. Arthur V. McAuley, D.D.S. 15186. Dr. Daniel Jacobs Long Beach CA 14655. Dr. William M. Pollack 60015 Deerfield United States 14646. Jim Aubrey DDS 14424. Dr. Agnes Guba MD Budapest Hungary 14354. Dr. Jan Becker 14227. Dr Vikki Petersen US 14177. Dr. Calvin R. George 1501 W. Lake St., Suite 3 Addison, Il 60101 14169. Anna C. Law, M.D. 14156. Paul Swanson MD 90027 Los Angeles CA USA 13945. Dr. Wayne King P. O. Box 13318 Anderson, S. C. 29624 USA 13726. Mary Ann Durham R. Ph. (TX) 5000 Georgi Lane Houston Texas USA 13433. Dr. Michael Teifke 12 Hibiscus road Belleair, Florida USA 13428. Dr. Katherine Zalin 91203 Glendale USA 13286. Dr. Arlen J. Lieberman MN 13222. Dr. Kenneth V. McIver 1310 Auckland New Zealand 13032. William T. Lohmann, D.D.S. 4176 Roswell Rd. Atlanta, GA 30342 USA 12898. Dr. Ron Nedd USA 12832. Dr. Paula K. Coffee As a dentist, I see the deleterious effects of psychotrip drugs every day in my patients. I am opposed to all psychiatric drugging of patients. What Eli Lilly has done to withhold the true side effects of these drugs is deplorable. Dr. Coffee 11031 S. Pikes Peak Drive, Ste. 103 Parker, CO 80138 USA 12768. Dr Neal Springer 12663. Dr. Bill Huggins 912 Drew Street Clearwater, Florida 12481. Dr. Michael Van Masters Scandal and deceit 80123 Littleton, CO 12267. G. Megan Shields, M.D. 12088. Ralf Blackstone, MD Prozac unsafe says doctor USA 12048. Dr. Karl Hoffower DC Sunnyvale, CA USA 11895. Arthur V. McAuley, D.D.S. 581 Pleasant Street 11890. Dr. Donna Shannon I feel that this is very important and must be investigated. 1638 Windsor Dr. Clearwater, FL USA 11873. Dr Zenon Duda I have personally known several people who came very close to killing themselves whilst on this drug 2520 Tulip Lane Cape Girardeau, Missouri USA 11748. Kathleen Gregg, RN as a practicing RN with over 30 years experience, I am in full support of correcting this injustice and creating uncorrupted research and ethical service uninfluenced by corporate greed to all patients and medical clients 90027 Los Angeles, Ca. USA 11501. Dr. Patricia Giuliano 11303. Kenneth Brent Olsen, Psy.D. Fresno, CA USA 11202. Howard Christofersen,MD As a physician, I strongly agree. 812 5th St` Anacortes WA 11034. Dr. Ronnie Freedman Helpline filled with callers who are having difficulties with SSRI medications, including Prozac. P.O. Box 11402 Philadelphia, PA USA 10959. denise-helene Adam n.d. 8--1680 Sherbrooke St East Montreal,Qc, Canada 10926. Dr. Zenon M. Duda 2520 Tulip Lane, 63701 Cape Girardeau, MO USA 10888. Dr. med. Heinz Lammert Wiener Str. 61-63, 60599 Frankfurt am Main Germany 10866. Nathaniel .S. Lehrman, M.D. 10 Nob Hill Gate Roslyn N Y USA 10861. Donald H. Marks, MD PhD 210 Lorna Square, PMB 192 Hoover, AL 35216 USA 10630. Dr. Dan Levernier 10598. R.A.L. van der Bijl, D.D.S. Amstelveen The Netherlands 10519. Dr. Bob DEmidio The insanity is the belief psychotropic drugs cure, when infact they mask the true causes, & with disastrous consequence. This petition is well within the scope of your offices & power of your charters to act . Please protect your charge. 95492 Windsor, Ca. USA 9950. Edwin S. Purcell, Ph.D. As a Neuroscientist, I emplore you to heed this petition. 9662. Jacque Bovee RN 9613. Dr Lawrence Retief 43 Linksfield Rd. Dowerglen Edenvale SOUTH AFRICA 9555. Julie W. Smith, DVM Prozac is dangerous as are most mind altering drugs 9532. David L. Rozeboom, D.C. 8420 Delmar, Suite 305 63124 St. Louis, Mo. USA 9374. Dennis W. Whitford, DC 9191. Dr. George Malnati 500 North Osceola Ave #410 Clearwater, FL 33755 U.S.A. 9188. Brenda A.Widows, BA, RN-Psyche Specialist it has proven itself to be a very dangerous drug 123 Dewey Ave. Washington, PA Washington 9096. Dan O'Shea, CPA Please help end the doping by Prozac 7439 Midland Road Cleveland, Ohio 44131 9074. Dr Bruce HARRIS As a doctor I urgently request this investigation 1221 Cleveland Street Clearwater Florida USA 9066. Dr. Michael Teifke Stop the insanity. 885 Millers Run Court Hamilton, Ohio 45011 USA 9006. Dr. James Aungst I have seen this drug and its clones ruin many lives. It should have been given to all Ely Lilly Execs and their families before it was unleashed on the public. 8925. Dr. Alfred Garbutt 8898. Dr. Ian Shillington PO Box 889, Datil, NM 87821 USA 8856. Dr. Craig E. Cowles 8798. Dr. Jerry Brady The truth needs to be revealed on this evil. Now is the time. $ billions are spent to convince us to take something that will do more harm then good. FDA needs to do it's job and protect those uninformed. USA 8778. Dr. Jeffrey Ptak Los Angeles, CA 8769. Dr. Paul K. Zollinger We have long allowed severe actions and methods on the mentally ill. Let them have rights like the rest of us beginning here. Maplewood, Mn USA 8683. Laurie Gelfand, BA, MA, RN New Jersey USA 8627. Dra. Ramona Alcántara Rep. Dominicana 8597. Dr. Katherine Zalin Glendale, CA USA 8550. Dr Carel Bredell I have looked into these allegations by talking to numerous family members of patients who have committed suicide whilst on Prozac. The stories are chillingly similar: The patient seems to be doing OK and then suddenly, out of character, committs suicide, even if most of them were not suicidal before going on the drug. If Eli Lilly knew about this, to then promote it is criminal. 8540. Dr. Arlen J. Lieberman 8445. Dr. William M. Pollack 60015 Deerfield United States 8403. Dr. Aharon Friedman Belleair, FL USA 8324. David Carothers, DDS 8227. Elizabeth Settle D.D.S. As a health practitioner I find this company's actions and products to be a gross disappointment to society and the medical industry! 8130. Dr. Harvey S. Reiter This is home-grown terrorism and deceit 20037 Washington, DC United States 8088. Dr. Anthony Rees South Africa 7708. Jerry Mittelman, DDS, FAPM 7293. Gottfried A. Lange, M.D. Germany 7220. Dr. Jean Hantman Feelings cure, meds stop feelings. 8025 wetherill rd cheltenham US 7167. Dr Neal Springer There are nutritional and other solutions that do not create the potential / actual damage of Prozac. This matter needs to be corrected ASAP. 90027 Hollywood 6895. Dr. William M. Pollack I've seen many patients become suicidal on this stuff 60015 Deerfield United States 6858. Dr. Stanley J. Zawada I urge withdrawing this drug from the marketplace. 12-57 150th Street Whitestone, NY 11357 USA 6852. Dr. Jesse Jutkowitz 06432 CT USA 6842. Dr. Christopher Kent 6794. DR. BOB DEMIDIO Ph.D. EE The use of drugs on children is a coverup & no solution for the failed school system of the past 30 years. We MUST turn the educational system around in this country or our infrastructure will collaspe. 544 Christopher Way Windsor, Ca. USA 6736. Dr. Kathy Biery 6705. Dr. Steven W. Martin, DC 6688. Dr. William B. Nicoletto This info needs to be brought out into public 6433. Dr. Stephen Paulette 129 University Boulevard Suite # E Harrisonburg, Virginia 22801 USA 6384. Mitch D. Carter, DC CA USA 6284. Dr Kristen Giles, D.C 6237. Dr.David E. Libs 6114. Luis Perez, Md Medical Doctor 15955 Paramount Blvd. Paramount, CA USA 6053. Dr. Kirk Youngman This is way overdue Danville Calif USA 6047. Dr. Joe Johannsonn I say NO to this legalized drug pushing. These psychotropic chemical creations are cocaine / heroin on steroids. Mother's little helper when the television isn't enough to numb the little ones who are too full of life. 00926-0123 Rio Piedras PR USA 5942. Det James, D.C. 5930. Dennis Nowack, D.C. tell the truth! Portland, Oregon USA 5914. Dr. Richard A. Mabanta 5892. Alan J. Lichter, DC Washington, DC USA 5885. Dr. Bruce Kesten for a safer America 11558 Island Park, NY USA 5785. DR KATIE E GREELEY D.C. 250 lombard st #4 thousand oaks, Ca. U.S.A. 5650. Dr. Joseph Graziani I have seen patients on prozac w/ harmful side effect. 5471. Dr. Marc D'Andrea 5463. Dr. Anita Mihlon 5212. KROISS, Dr. (MD) Thomas G. very important to get unaddicted and free thinking people! 5132. Dr Adrienne Hall 4912. Neil R Woods DDS 4721. Dr. Jeffrey Ptak 1127 Wilshire Bl. Santa Monica, CA USA 4634. Dr. Christine Carlyn Henry, Ph.D. 4563. Rosalie M. Williams R.N. 2231 Colts Neck Rd. #515 Reston VA USA 4439. Dr. Scott DeMent 8793 E Broadway, 85710 Tuscon, AZ USA 4320. Dr. rer. nat. Philipp Sonntag please recognize mental terror as crime Lepsiusstr. 45 D 12163 Berlin Germany 4277. De Ann Beig Omaha, NE USA 4241. Lauren Fecher, R.Ph. As a pharmacist for 20+ years I can wholeheartedly endorse this petition. 4233. Dr. Katherine Zalin PO Box 10896 Glendale, CA USA 4135. Paul Swanson, M.D. As a medical doctor, I can attest this drug robs people of their humanity. They become flat. A very common comment is, "It takes away the highs and the lows ." San Francisco CA 4049. Dr Rene' Reed Clearwater, FL USA 4031. Dr. Stephen Ziegler 7915 Malcolm Rd., Suite 100 Clinton, MD 20735 US 3935. Dr. James Gatza I have not seen positive observations of my patients who have been taking prozac 3898. Scott F. Futch, DDS Michigan USA 3880. Glenn Nozek, D.C., FIACA 08753 Toms River, New Jersey United States 3872. Teri Crowther,RNC My teenage depressed son was on it. 3838. Dr. Terry Lynch I fully support this petition Limerick, Ireland 3832. Dr. William B. Nicoletto 3816. Dr. Ralph Minogue Let's not stop at Prozac 85635 AZ USA 3789. Sheri Reid, R.N. 2201 Garrett Morris Parkway Mineral Wells, Texas 76067 USA 3722. Eric Berg D.C. 4609 D Pinecrest Office Park Drive Alexandria, VA 22312 USA 3718. Dr. James D. Knight 513 West 2600 South Bountiful Utah 3696. Dr. Guy Wilson "Health is simple, get the good in and keep the bad out."...any questions? 1762 N. Waterman Ave. San Bernardino, CA 92404 3649. Rodney M. Person, RN 504 W. Washington St., 16407-1465 Corry, PA USA 3640. Dr Bill Gallagher, DC Scottsdale, AZ 3630. Dr. Kathy Biery 129 University Boulevard Suite E Harrisonburg, VA 22801 USA 3609. Ann Blake Tracy, PhD Utah USA 3509. Dr. Jennifer R. Rice These drugs are way over prescribed and are dangerous to the person and those around him or her. 3293. Dr. Angela Price Kloss they need to pay! 3224. Dr. David Stedman 3044. Lauren Fecher, R.Ph. Austin, TX USA 2968. Michael A. Walby, O.D. Prozac should be banned completely 404 E. Ash St. Perry, FL USA 2941. Mehran R, Sorouri, D.C. 2870. Dr. George E. Springer, Jr. 2688. Richard W. McBride, D.C. Pennsylvania USA 2539. Baxter W. Paschal, DC 677 S. Bennett Street Southern Pines, NC 28387 USA 2428. Katharine M. Conable, D.C. Drug companies should separate themselves from psychiatry's false labeling of patients and fraudulent research. They should stick to making medicines for real medical conditions, and improve their quality and research integrity. 851 Warder Ave. St. Louis, MO USA 2304. Robert J. Seaman, Jr. DDS 670 E. 1250 Rd. Lawrence, Kansas USA 2302. Dr.D.yawrenko 2288. Dr. Mark Baxter Las Vegas, Nevada 2135. Dr. Arlen J. Lieberman 5685 Dduluth Street 55422 Golden Valley, MN. USA 2095. Dr. Mark S. Valinsky It is important to get this drug and its related combinations off the market to protect public safety 1987. Dr. Philipp Sonntag I have seen many drugged victims; Prozac is an outstanding crime Lepsiusstr. 45 in 12163 Berlin Berlin Germany 1796. Richard Walicki, DMD Philadelphia, PA 1764. Bert H. Brooks, DVM Prozac and other serotonin re-uptake inhibitors are also used in animals. In one hundred percent of the cases we have tested where SRIs were used by other veterinarians to cause changes in behavior, such substances have proved to be unnecessary. When proper nutritional supplements are used which address the central issues of the patients, SRIs are no longer ”needed.” Prozac and the rest of the SRIs work by suppressing symptoms of problems not by solving the problems. 15200 County Road 96B, 95695 Woodland, CA USA 1602. Clinton R. Friday, D.C. I believe there is sufficient evidence, of both an objective and subjective nature, to investigate this drug. There is an obligation to inform all as to the potential effects of the medication. 1548. David L. Rozeboom, D.C. 8428 Delmar, 63124 St. Louis, Mo. 1107. Steven J. Karageanes, D.O. USA 1049. Allyne Rosenthal, D.C. 122 S. Michigan, 60603 Chicago USA 626. Dr. Katherine Zalin 319 N. Kenwood Street #3 Glendale, CA USA 573. Jeannette K. Buckles, DMD Clearwater, Florida USA 543. G. Megan Shields, M.D. I have seen murder, suicide and attempted suicide from the drug Prozac in my practice. I have never seen this with any other drug. Prozac should be removed from the market. 5336 Fountain Avenue Los Angeles, CA 90029 USA 363. Dr. Gary Farr 41. Dr Robert Simonds This is a deadly drug used on kids (ADHD) P.O.Box 3200 Costa Mesa, Calif. U.S.A. | |
Posted by Linda, 10:23 30 April 2007SSRI Warning
Public Notice There is a class of drugs on the market for depression, anxiety, and a host of other mental health problems known as Selective Serotonin Reuptake Inhibitors, or SSRIs. You have heard of them: Prozac, Paxil, Zoloft, Luvox, Celexa... to name just a few... If you are currently on one of these drugs, or if someone has mentioned to you that you should get on one of these drugs (your family physician, your friend, your relative), this notice is especially for you. SSRI theory is based on findings that depressed people have lower levels of the metabolite of the neurotransmitter serotonin. SSRI drugs block the re-uptake of serotonin in the brain, and thus, the level of serotonin increases in the brain, bringing about the "proper" neurotransmission necessary to alleviate the depression. This is a horribly flawed theory. Some of what the companies manufacturing these SSRI's, and what doctors prescribing this medication will very likely NOT tell you is this: The Merriam-Webster online dictionary defines serotonin as, "a powerful vasoconstrictor", which is what it was discovered to be in 1948. A vasoconstrictor is an agent which constricts blood vessels and blood flow. So while shoring up enough of the neurotransmitter serotonin in the brain to alleviate depression, the person taking one of these drugs is also shoring up enough of the vasoconstrictor - serotonin, to substantially decrease blood flow in the brain- a serious and sometimes deadly oversight. And, as the delicate chemical balances in each of our brains is as unique to each person as his or her fingerprints, it's no surprise the adverse reactions reported with these drugs can vary to extremes. Some people have seizures while either actively taking, or while withdrawing from these drugs. Some people have had strokes after taking them, due to the vasoconstrictive action of too high a serotonin level. Some experience a complete personality change. But another serious casualty of this decrease in blood flow concerns the area of the brain responsible for self-control. This is why nearly every time you hear of some random, violent act such as a school or office shooting, the people going into these homicidal rages have been found to be on an SSRI over 95% of the time. Columbine High School? One of those kids was taking Luvox. The Atlanta day trader who shot up his office? Prozac. Kip Kinkel? Prozac. Michael McDermott in Boston? Paxil and Prozac. Phil Hartman's wife Brynn had been taking Zoloft before killing her husband and herself. These are just to name a few. A jury in Gillette Wyoming determined that Paxil was to blame for a triple murder/suicide. The plaintiffs were awarded an $8 million dollar settlement in this case which hit the media during the first week of June 2001. Unfortunately a money settlement, no matter how large can ever bring back four precious human lives! In another case in Australia, a supreme court judge found Zoloft to be the reason a fellow murdered his wife of over 30 years... For every one of those incidents you have heard about, there are fifty such incidents that didn't make the national news. But wouldn't the FDA keep something like this off the market? No. There is simply too much political and financial interest in the profits from these drugs. Your consumer protection when it comes to this class of drugs is just not there. People within the FDA who have dared to voice opposition to these drugs during the approval processes have found themselves without their jobs. During trials to determine the safety of Prozac, when subjects were reported to have become suicidal on the drug, a memo surfaced, ordering the language in the report changed from "suicidal" to "depressed". Further, the FDA issues "conflict of interest waivers" to drug company doctors and researchers during the approval processes for these drugs. For example, in the case of Paxil, every single one of the "experts" on the panel with the authority to approve or disapprove Paxil had been granted this "conflict of interest waiver" by the FDA director. As a result, Paxil was approved as safe. Safe, for say, a mother of four driving her kids down the interstate at 75 mph - while the Federal Aviation Administration will not grant a pilot's license to anyone on Paxil, because the seizures and sudden involuntary movements it can cause may cause a pilot to crash a plane. We say SSRI's are NOT safe, and there is account upon account to back it up. Just who are 'WE', you might be asking yourself... We are a group of people who have taken these drugs, only to have them upend our lives in a variety of some of the worst ways imaginable. And we want you to know what they do. | |
Posted by Linda, 10:24 30 April 2007The story of B
Below is my son's story as I submitted it to the FDA before the most recent hearings: Our son, B, had it all - good grades, good looks, popularity, tremendous athletic ability and a bright future. Add to that a beautiful, smart fiancée and everything should be perfect, right? Wrong! B was always what we described as "high maintenance" or "high-strung." He was very bright, opinionated, and articulate. If he disagreed with something that happened at school (like another kid being picked on, an unevenly applied rule or punishment, etc.), B. was the first to stand up and speak his mind. He was meticulous in everything he did. He had to succeed. Anything less than total success was utter failure. We called him "Stat" because he could quote football and other sport statistics at will. He was very opinionated, stubborn and easily frustrated but, for the most part, he kept it under control. He sailed through high school on the Honor Roll and was awarded such distinctions as "Athlete of the Year," 3-time "Who's Who Among American High School Students," "All-District" in Cross Country and Track, "High Point Champion" at several area track meets (extremely rare and difficult for a distance runner) and 9-time Arkansas Junior Olympic Gold Medalist. He ran the anchor leg of the Arkansas State Track Class AA 4x800m championship in 2001. He ran cross-country for his high school. His team placed 2nd and 4th in the State Class AAA Cross Country Championship the 2 years he ran. He competed in the National Junior Olympics Cross Country Meet in Chicago, placing in the middle of the pack of more than 300 racers. In 2001, he received a partial scholarship to Bacone College in Muskogee, OK for track and cross-country. That's when the trouble began. He was trying to maintain his grades, train and compete in cross-country, work part-time and see his fiancée - she lived about 3 hours away from Muskogee and he traveled to see her when he could. He became increasingly stressed and began to talk of dropping out of school. He said that it was just too much for him to handle. We stressed the importance of a college education but allowed him to transfer to a community college in Fayetteville, AR where he would be in the same town as his fiancée. While things weren't perfect, B and Jenny were happy until B's great grandmother died in June of 2002. B lost his job because he took off from work to travel home and attend her funeral - his boss was on vacation, which left B in charge of the store. Losing his job meant that he and Jennifer couldn't afford to keep the house they were renting. Jenny was working, too, but with both of them trying to go to school and work, it was too much. They moved back home to southern Arkansas later that summer. B was not happy about moving home and became increasingly angry and resentful. We talked to him about his attitude and things seemed to be okay for a while. He and Jenny had an old home that she had inherited but it needed a lot of work. B decided to drop school for a year and work full-time while Jenny worked full-time and went to college part-time. He was working for the county road department when he got into a huge patch of poison ivy and was covered from head to toe with welts. The doctor put him on a double round of corticosteroids to help. He was out of work for 10 days and never really seemed to be the same after that. He became even more easily angered. He couldn't relate to us why he was so angry. That's when I made my big mistake. His attitude was straining our relationship with him, as well as his and Jenny's relationship. I acted as objectively as I could and supported his and Jenny's decision that he should move back home with us while he got a handle on things. I also told him about a website I had seen - www.effexorxr.com. I had already visited the site and was alarmed by the results from the answers I had entered into an online survey from my perspective on B's behalf about depression. I asked B to complete the survey for himself and the results were even worse that when I had answered for him. He was urged to "seek professional help" for his problems. I encouraged him to go to our local mental health facility and enlisted Jenny's help in getting him to go. He followed our advice and began seeing a psychologist. He got to talk about his frustrations and his reactions to stress and obstacles. Things seemed to be getting better. He was asked to keep a journal of his thoughts and feelings. Then after a couple of months of talking to the therapist, she referred him to a psychiatrist at the main office of the mental health center which was in a neighboring county. He said she told him that he had completed the "intake and assessment" process. Now it was time to get down to "treatment." B was extremely upset when he came to my office after his first visit with the doctor. He said that when he walked in, the doctor was raging at his receptionist for overbooking his schedule. Apparently, he had lunch plans that B's appointment was interfering with. B told me that the doctor grabbed a stack of papers from his fax machine and began to read them over. The papers were B's records from the psychologist. After a couple of minutes, the doctor told B that he was suffering from depression and handed him a large grocery bag full of samples of, ironically enough, Effexor XR and a sleep aid. He told B that it would take several weeks to know whether the medication was the right one for him and that they might have to switch brands if this one didn't work. He told him that it takes awhile for a person's body to adjust to the drugs, but to be patient. He scheduled another appointment for a week later and sent him out the door. He put B on a schedule that would increase his dosage from 75 mg per day to 300 mg per day over several weeks. The sleep aid was for insomnia that the doctor said was a common side effect. B felt slighted by the lack of time and care that the doctor exhibited but said that he was going to take the medication because he wanted to be his old self again. From the very first dosage, B was a different person. His mood swings became much worse. He would rant and rave at us, then not appear to remember what he had said. He started binge drinking. He started telling me of horrible nightmares and daydreams he was having. Dreams of killing me, his step-dad and Jenny (not his sister for some reason); impulses to run into other vehicles head-on on the road. I was, of course, alarmed. I called the mental health center to express my concerns and was promptly told to mind my own business. B was an adult and it was none of my concern, she said. She told me that he "had a number he could call" if he felt like he was in crisis. I explained that he was telling me that they were trying to poison him and that he said he wasn't going to go back. She told me that I should call the police if I thought he was out of control. No mother wants to call the police on her son, especially if he is not committing a crime. I was under the impression it was a problem adjusting to the medication that should lessen as his body became accustomed to the drugs - besides, during upswings, B was telling me that he felt so much better and could "see clearly" what he had to do. He said that he would go back to the counselor and he did. He re-enrolled in college, got a new job and, for a few days, seemed to be doing better. Then he freaked out again and it became a vicious cycle of ups and downs. Anger and crying spells. He was so confused. Then - like magic - he would feel great again. We would stay up all night.talking, crying and trying to figure out what to do. Up, down, up, down. It was a dizzying spiral. After much discussion.many all-night talks, B agreed to find a job and re-enroll in college. He did this within a couple of days of agreeing to. Once again, I thought he had found a stable level. However, the night of September 2, 2003, he had a bad night again. We talked, cried, and talked some more. He said he was just so confused about everything. Sometimes he thought the medication was the only thing helping him maintain his sanity; other times he knew the medication was causing him to think about becoming a murderous monster. "When would it level off?" he begged of me. He told me how sorry he was for all the trouble he had caused. It all came to a tragic end the next day, September 3, 2003. I had gone to an out-of-town meeting and came home about 3:30 p.m. with a headache. I spoke to B about how he was feeling - "Fine, I've got my head together now. I know what I have to do to fix things." were the last words he said to me. I went to lie down for a while. About an hour later, my husband woke me up - he couldn't find B (who should have left for work by 4:00 p.m.) Our daughter told us she had seen B petting our dogs in our yard and then walking towards our wooded acreage. My husband ran to find him thinking that he had gone off to think and had lost track of time. That's when he saw it. The rope we used to close one of our outbuildings had been tied from the inside. He cut the rope and found our beautiful son hanging by a rope. He was neatly dressed and shaved. His work uniform was folded neatly and placed on the seat of his truck. He had 21 suicide notes tucked into the waistband of his jeans. His memorial service was beautiful. We played his favorite modern rock music.Godsmack, Stain'd.and "our song" Lynard Skynard's "Simple Man" which I used to sing to him when he was little as he stood on my feet and we danced. Many kids, parents and others he knew gave testimonial after testimonial about how B had helped them deal with their problems.how B would always stand up for the underdog.how B had been an inspiration in so many ways. I had to find out why we lost him. His journals spoke of having horrible thoughts after he started taking the Effexor.of how the pills made him feel numb and how he could tell when each dose was "wearing off" because those evil thoughts became very compelling. He wrote in his journal that he wouldn't ever be the kind of person his mind was telling him to be - violent, hateful, murderous. He described vivid dreams of killing those closest to him - me, his step dad, Jennifer. He stated that the medication had helped him see that he had to die to keep this from happening. I didn't know that the drug companies' data shows these drugs to be about as effective as a placebo. I didn't know that there is no test to determine whether there is or the extent of the "chemical imbalance" the drug companies claim SSRI/SSNRI drugs treat. I had never heard of "activation syndrome" - and obviously neither had the "professionals" I sent him to - but now I know that's what happened to him. The ever-increasing dosages of Effexor XR made him unable to function; it made him decide that suicide was the way to keep from becoming a monster. Then I read of people on these drugs who had killed; people who described the same types of thoughts and dreams B did; mothers who drown or cut the arms off their babies...children and teens killing classmates in school shootings while on these drugs. Columbine. Andrea Yates. Christopher Pittman. And I thanked God that we had only lost him to suicide and not to prison or the death chamber after a homicidal rampage. I see people all around me who are taking these drugs. Some of those close to me (through personal and work relationships) have actually started taking these drugs despite information I have shared with them. The media will cover tragic stories like Christopher Pittman, Cody Posey, Andrea Yates, etc. - but once their trials are over, no one in the media puts the pieces of this puzzle together and demands to know why these tragedies keep occurring. No one questions the motives of the companies who keep selling obviously dangerous drugs. No one questions the competency of the doctors who prescribe them. Eventually, over the past few years, the FDA has taken steps to warn people about the effects of these drugs.first for children, then for adolescents, then during the beginning of treatment. It is time to recognize that the only way to prevent the side effects of these drugs is to ban them. We urge you to do so. | |
Posted by Linda, 10:25 30 April 2007The story of H.
I'm a 22 year old student. My studies had gone very well and university life was generally successful in every respect. However, I had had a few problems and felt tired and had a lot of stress. My doctor diagnosed me with depression after a very brief consultation, and suggested i take Prozac. Looking back now, i did suffer from depression, but I think my problems would have resolved with time, and it was nothing compared to what the SSRI's induced. After being told that Prozac has very few side-effects, I agreed to try it. The reaction started very soon after the first dose....within 48 hours I felt the usual nausea, headache, dizziness. Within a few days, i suddenly felt extremely anxious and a worsenning of depression....this developed rapidly into a depression deeper than I had ever experienced before. I felt extremely confused and for no reason, believed everyone to be against me. This sudden worsenning of mood was accompanied by strange physical symptoms; my skin was itching, my mucsles were twitching, i was shaking violently, and felt a terrible pressure behind my eyes....everything looked brighter and my thoughts were racing. I was put on another SSRI a few days later after a emergency doctor had to be called...... I had felt a sudden panic worse than anything I had ever experienced, i felt strong impulses to do things that I didn't want to do and the fear was extreme. I was so afraid of myself and really thought that I'd lose control .The doctors persuaded me that I should stay on the medication for longer and that the symptoms I was experiencing were a worsenning of my depression. Over the following three months the doctors prescribed another two SSRI's.. There were a couple weeks when I believed the medication to be finally working....I felt really confident and excited, almost euphoric. I was unable to eat or sleep, I lost a lot of weight, and then very suddenly my mood changed again and I felt very strong suicidal impulses. The terrifying side-effects continued and I eventually decided to stop the medication. I was unaware of the dangers associated with abrupt withdrawal. Some of the restlessness eased a few days later, but most of the symptoms remained. I was unable to study anymore, the anxiety was so great, and I had no concentration. I couldn't feel normal emotions anymore, nor could i think clearly. A psychiatrist whom I had been referred to suggested that I go to hospital for a few weeks.....i was unable to function and desperately wanted help. In hospital I refused any more anti-depressants, i knew that the damage had been caused by the drugs, and decided to allow time to heal me. Seven months have now passed since my last SSRI dose and although I am getting better, the process is very slow. Although the doctors finally recognised that I had a bad reaction to the SSRI's, they have all dismissed the idea that for some people they can cause long-term damage. Because of the reaction, I had to discontinue university. I'd do anything to be the person I was before i took SSRI's. All I want is to be able to continue at college, and fulfill my aspirations.... but I am confident that with time I will get better and hopefully be a stronger person at the end of it. | |
Posted by Linda, 10:26 30 April 2007The story of N
22 years ago, my husband was diagnosed as "paranoid schizophrenic with bipolar disorder", effectively ruining his plans as a recent Stanford University graduate. Over the next 12 years, he was hospitalized many times, and had many pharmaceutical drugs forced on him. He endured abuse as well, at the hands of psychiatric ward workers, including being strapped to a bed for 68 hours straight and not allowed even to use a restroom, then ridiculed for soiling the bed. Shortly after we married 10 years ago, he had another episode of schizophrenia. I had no idea what to do, and thought one was supposed to let "the professionals" handle it (HAHAHA!). One thing that was recommended to me was to call the police (???) and have them put a 72 hour hold on him, so the psychiatric ward could administer electroshock. This went on and on!! Long story short....we found a clinic in Naperville, Illinois called Health Research Institute and Pfeiffer Treatment Center (www.hriptc.org) who did not treat him like a criminal or an imbecile, and also did not treat him with pharmaceuticals. He does mega vitamin therapy, which worked within 3 days, and has had no symptoms, no drugs (no side effects!), and no problems for 10 years now. A book we used to get him stable enough to visit the clinic is called "Natural Healing for Schizophrenia" by Eva Edelman. I don't know what we would have done without this book, and it completely changed the way I saw medicine and health! | |
Posted by Linda, 10:26 30 April 2007The story of C
I am neither a psychiatric survivor, nor a member of the Scientology Church. I have never been prescribed, nor have I ever taken a psychiatric drug, but my life has taken a complete 180 degree turn because of them. I carry no high degrees or honors worthy of applaud or recognition. I am just a mother who cares about this world and my fellow man. I care deeply about human rights and free agency. My ex-husband was prescribed Paxil to alleviate depression. Initially, he had a positive response to it, but that effect did not last. When my son was only twelve years old I was told that a “chemical imbalance” was the cause of his depression. He was prescribed Prozac by a physicians assistant in our primary care doctor’s office. Our doctor explained that depression runs in families (like father, like son). My son told me he didnt want to keep taking this drug because it made him feel really “weird.” When we discussed this with our doctor, he told us that sometimes it is hard to find the proper dosage for children, but since my son was big for his age, he doubled the dosage. One day I found my son no longer breathing. He had died from a self inflicted gunshot wound to the head, or at least that’s what his death certificate tells the world. I eventually came to know of others who had experienced negative results from using antidepressants, and my ex-husband decided to quit taking Paxil. We had been married for nearly twenty years, and had faced different challenges throughout that time, but nothing could have ever prepared us for the nightmare we lived through as he tried to come off Paxil. He became violent and suicidal. Our marriage fell apart during that time. It took almost a year before he was certain that he was free from the horrendous withdrawal. He has never been violent or suicidal since. Through my own research I discovered that there is no definitive test that can determine whether someone has a chemical imbalance. My personal understanding has been validated by the scientific literature. So, essentially, we had been lied to by the physician we had once trusted. No doubt, he had been lied to and trusted pharmaceutical reps he had once trusted. The FDA has miserably failed in its own stated mission: ”The FDA is responsible for protecting the public health by assuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our nations food supply, cosmetics, and products that emit radiation. The FDA is also responsible for advancing the public health by helping to speed innovations that make medicines and foods more effective, safer, and more affordable; and helping the public get the accurate, science-based information they need to use medicines and foods to improve their health.” I personally testified before an FDA hearing on the safety of antidepressants in February 2004. I have read the transcripts from the 1991 and September 2004 hearings. It has now been sixteen years since the first horror stories were laid bare for the FDA to examine, and during this expanse of time, the FDA administration has not yet met its own missive, and thousands have died or have been through similar nightmarish experiences to my own. I am not writing to request additional restrictions on these drugs or more strongly worded warnings. I am writing because it is time for those who head the FDA to step down or be booted out. It is well past time to change the guard. | |
Posted by Linda, 10:27 30 April 2007The story of L
My wife suffered major, disabling depression for 15 years. At first we tried the traditional anti-depressant approach. She was tried on just about all of them. One of them almost killed her by destroying her liver, one caused her to become extremely suicidal, one turned her into an unfeeling zombie, at least one caused extreme anxiety and agoraphobia. She was then priviledged to be part of the Cymbalta test program. Cymbalta caused her tongue to break out into white painful sores that hurt so bad she couldnt eat, and when the doctor took her off the drug the day after, she collapsed and was literally paralyzed from the neck down for about 6 hours. We had to take her to the emergency room. At this point we finally said no to the drug route. We went to a doctor who treats people with alternative medicine and discovered her true problem: severe hormone imbalance, hypothyroidism, and extreme adrenal fatigue. To make a long story short, she is now off all drugs except armor thyroid. She takes herbs for her adrenals and uses progesterone cream. Finally after over 15 years I have my wife back. Drugs are not the solution. To treat depression you must first find out the underlying problem. My personal opinion is that depression is not an illness, but a symptom. In my wife’s case it had to do with the whole endrocrine system being imbalanced. In fact, I would be willing to bet that the majority of depression cases have some link to this disorder. It took a lot of experimenting but it was worth the effort. It was my wife’s case that set me on the path of natural medicine. My desire is to get the message out: Do not rely on antidepressants, they are at best a temporary cover up of the symptoms. Find the cause and correct it and you can have a normal life without drugs! | |
Posted by Linda, 10:28 30 April 2007The story of S
Hi.. I would like to share some of my story. I am 46, an attorney, mother, grandmother... In 1984 I was put on tricyclic antidepressants while my husband struggled with leukemia. The doctor wanted to take advantage of the side effect of weight gain, as I was not eating properly. I became aggressive and impulsive, but managed to complete a law degree. I stayed on the antidepressants. While studying for the Bar in 1994, I was switched to SSRIs (Zoloft). Within weeks I developed panic attacks and my diaphragm partially paralyzed. They added benzodiazapine. In 1996, I attempted suicide. They diagnosed me with bipolar disorder based on the aggression and suicidality. They put me on anticonvulsants. The aggression went away. And my nightmare began.. Over the next ten years, I put on 100 pounds, developed high blood pressure, high blood sugar, an ulcer, heart and lung problems, neuromuscular problems, mild hallucinations. I probably was tried on 15 different medications during this time as they all had unacceptable side effects or didn't work or made my symptoms worse. But they assured me I just needed the right combination. I didn't want to go back to being angry and impulsive, which they attributed to bipolar disorder. So, I continued to try medications. In 2002, I began stumbling and had several falls between 2002 and 2005, resulting in permanent spinal damage. In 2004, I was hospitalized for pneumonia and was in the hospital for a month. I was in isolation for 9 days due to heart palpitations, severe sweating, neuromuscular problems. They thought I had tuberculosis. It was later found they had neglected to give me some of the medications and I was having "discontinuation syndrome." I was put on oxygen 24/7 for several months, then "while ambulating" as my paralyzed diaphragm was collapsing one lung. They changed me to a new antidepressant, Effexor. A few months later I took a near fatal overdose. I was unconscious 4 days before my family convinced the police to check on me. I was lucky I did not suffer brain damage. They switched me to Celexa and added Seroquel, an antipsychotic, to help me sleep. In 2005 I became so disorganized and suicidal my employer became concerned. I admitted myself to a psychiatric hospital for the first time. I refused to leave til they "fixed me." At that time, they discontinued the anti-anxiety and anti-psychotic medications. I went through several days of panic and sleeplessness, but I recovered. Then over a period of several weeks, they decreased the SSRI, believing it was making me more depressed. The plan was to leave me on only an anticonvulsant. I developed severe muscle pain, nausea, vomitting, convulsions, tinnitus, nystagmus, laughing and crying spells, panic, sweating, electric shocks in my arms and head. I lost my job, as I could not return in that state and they could not accommodate my absence. I was in and out of the ER. My family doctor finally said to go off ALL medication. ALL chemicals as he thought my liver and gallbladder were failing and they might have to remove the gallbladder. He ordered an abdominal scan and referred me to a liver specialist for liver damage. However, when I lost my job, I lost my insurance... So, I consulted a naturopath. She had me do a liver and gallbladder cleanse.. I threw out all packaged food and switched to organic, fresh everything. This was the first week in March. I felt deathly ill for three weeks. But slowly, I began to feel better. The suicidal thoughts went away. The muscle pain and contractions went away. My blood sugar and blood pressure returned to normal. My ulcer went away. I lost 76 pounds. I began breathing better and was able to discontinue using a bipap and oxygen at night. I have been off all medications since March. I still haven't found a full-time job, have had to sell my home, and theoretically should be depressed and suicidal, as that has been my mental state for ten years.. yet I am fine. No depression. Even the anxiety is minimal for someone in my precarious circumstances. I believe that these medications caused the symptoms that led to the diagnosis of bipolar disorder; and the subsequent prescriptions caused the whole host of illnesses that cost me my job, my home, and so far, it looks like, my career. I have relocated to another state, hoping to find work here, as my education and experience rendered me over-qualified for anything other than attorney work and the flooded market and other factors have prevented me finding work in my area. I hope that my experience will help others to understand the hazards of the pharmaceutical complex as it stands. | |
Posted by Linda, 10:29 30 April 2007The story of A
I started treatment for depression 18 months ago. I was taking Ativan at the time for depression. I was put on Serzone for many months, had my dosage steadily increased until I was up to the max of 600 mg a day. It didn't put a dent in my depression, and I gained so much weight that I asked to be taken off. I was put on Prozac for 3 months .. I became another person ... dead to the world, and craving alcohol, and even more depressed. Thats when I was put on Effexor. At first I felt the positive effects immediately .. I had energy, I was happy, I thought this was the greatest drug in the world. Then IT started to happen. After a few months on Effexor, I started to become very tired all the time. I slept as much as 18 hours a day. I stayed in my house. My anxiety became worse & worse until it was even difficult to go to the store. I couldnt eat, I had no appetite, and when I did eat, I threw up violently. I also had the 'runs' for months. I started getting dizzy all of the time, my heartrate was at about 130 bpm constantly, and I had to start taking heart medication to calm that down. Gradually I became sicker & sicker ... I started having wierd shock sensations throught the day, terrible dreams that I couldn’t distinguish from reality, and I became numb .. so numb that I didn’t even put up a Christmas tree this year for my kids.. I didnt even attend my family's get-together. I was too sick to function at all. I had trouble breathing all of the time too. I went to see my family doctor & he could find nothing wrong with me. He pretty much told me that it was all in my head. Of course he did do some tests on me - but all came out ok. I decided that I was just crazy, and it was all due to depression, UNTIL the night I stayed up all night watching rental movies with my son & his friend. I slept very late the next day, well past noon, and well past my normal 6 a.m. dose of Effexor. OH BOY .. was THAT ever a day of awakening. When I awoke .. ALL of the above symptoms were 10 times worse, and I knew then that it was related to Effexor. I took my dose & felt better after a few hours. I started researching on the net .. and found the withdrawal message board (unfortunately, it is no longer there) ... I couldn’t believe what I read. Right there in black and white was my nightmare OVER & OVER. WIth every page I read, I became more determined than ever to get off of this drug. I now know that I was suffering from tolerance withdrawal. I went to talk to my psychiatrist .. he wanted to UP my dose. I said NO WAY .. I want off. He gave me Wellbutrin & told me to take that for 2 weeks, then stop the Effexor cold turkey. I said, 'what about withdrawal from the Effexor?' he said 'we rarely see that - you will be fine'. I took the Wellbutrin for 3 days .. it made me want to jump out of my skin ... I was even sicker .. I stopped taking it & went back to the doc. He gave me Paxil that time(another addictive drug). I talked him into giving me some 37.5 Effexor pills for a taper. I took Paxil for 3 days .. and I slept the entire 3 days. I became a zombie & started to believe I was incurable. By this time, I had HAD it. I decided to take myself off of the Effexor & go drug free. I dropped to 37.5 for 3 weeks. I had withdrawal. Vomiting, shocks, vertigo, etc ... but I noticed that I could breathe better, and I wasnt vomiting as much at that dose. After 3 weeks, I took half the granules out of my 37.5 pill, that same day I got so sick that I couldn’t go to work. That is when I braced for the storm & went cold turkey. I lost my job - but it was better than losing my life to this drug. That was 4 weeks ago. The withdrawals were horrible the first week. I shook, I cried, every time I moved my eyes, I would get severe vertigo & electric shocks running through my entire body. I couldn't take a shower, for fear of falling & hitting my head. I couldn't drive, and every single noise sounded like a atomic bomb to me. The only comfort I had were the people here on the internet. I called my family doctor, he didn’t believe in the withdrawals. I called my psychiatrist... they said 'TAKE ANOTHER PILL'. Oh my god .. I wanted to just die. I began having panic attacks that would last for hours on top of all the other symptoms. My neighbor had to go get groceries for me, and my son, my poor son, just looked at me in horror. I became suicidal at about the 4th day. I had to call my neighbor to come over. By day 8, I went to get acupuncture on two consecutive days to relieve my anxiety. (I had never done this before, but I was deperate - it worked ! for those two days) The dreams I had during this time were ALL about dying..becuase I thought I was dying .. I WANTED to die. By the sixth day some of the symptoms became milder ... at 2 weeks...my brain started to feel clearer, I didn’t feel so numb anymore, the shocks & anxiety were still there. Now, at 4 weeks, I am still having major anxiety problems, panic attacks, some vertigo .. and I get the shocks when I am really tired. My memory seems really bad & my vision is blurry. I will have a couple of days when I feel really good, followed by 3 or so days of going backwards. The good news - I can laugh again, I can think more clearly, my appetite is back, I am losing weight slowly, I don’t vomit anymore & I dont have the 'runs'. I actually had a few GOOD dreams this week .. but also had some very scary ones. Sometimes I am terrified, because I don't know what this drug has done to me. I feel permanently damaged. My short term memory is gone, I have sudden mood swings, I could sleep for a week if I didn't have to get my son up for school. I am finding this all to be very disturbing, as I thought that once the intital withdrawal was over, I would feel like myself again. I am starting to think I am going crazy. I realize that it takes time for all of the brain chemicals to stabilize again .. but how long ? I don't feel mentally capable of going back to work & I am running out of money.I fired my psychiatrist & I am now seeing a doctor that specializes in anxiety. I am nowhere near the person that I was before all the drugs. It’s really sad, to think that you are doing the 'right' thing for yourself by listening to these professionals, only to find that you are slowly becoming what they THOUGHT you were in the first place. It’s like they diagnose & then turn you into that 'thing' with all the meds. I hope that this ends soon. I am hoping to get my life back....and that will take even longer. | |
Posted by Linda, 10:29 30 April 2007The story of D
About 7 months ago I suffered a panic attack, which I didn't handle too well. After seeing my md a few times I was put on Cipramil and told I would feel myself again in about 4-6 weeks. About 2 weeks into the meds my panic attacks worsened - I had really hot surges rushing through my whole body. Not to mention horrible nightmares and obsessive thoughts that I was going to lose it and kill somebody. I'm still traumatised and plagued by these thoughts and believe me I was NEVER a violent aggressive person. My pdoc assured me it wasn't the medication but part of the depression. I kept on taking it. I went back to work about 4 weeks into the med and started noticing that I didn't feel real anymore. By the 6th week I was an absolute zombie, emotionless, physically numb - I couldn't feel the water running on me in the shower or taste food. I arrived at work one morning and felt like I didn't know where I was or how I got there. I broke down and haven't been back at work since (that was about 4 months ago). The psychiatrist told me it was the depression that was making me feel this way, but also made me stop the Cipramil cold turkey. That's when another nightmare began. Severe dizziness, to the point where I felt like I was going to pass out or lose control, I even slept with the light on because of the fear. At the time I didn't know it was withdrawal...thought I was losing my mind. That lasted for over a month, never really subsided. I then saw a naturopath with no success. I now know that I was still suffering from withdrawal, but thought it impossible at the time - 2 months later, so I went to another pdoc and was given Zoloft, was on that for 6 weeks, have been off it almost 4. I'm now suffering hellish withdrawal AGAIN. Feel really disconnected and drugged out most of the time. Have heart palpitations, tightness in the head, dizziness, tinnitus, flashes of memories and images. I feel as thought a part of me has died. Find it hard to believe that I was anything but this person, nothing feels real anymore. These drugs have taken my identity, destroyed my relationships with friends and family...made me unable to function like a normal human being. I have completely lost my grip, hate to go out and be around people. Don't even feel comfortable with my family. I've been taking vitamins and St.John's Wort to try and help with detox, but still the nightmare continues. Sometimes it feels like it will never end. | |
Posted by Linda, 10:30 30 April 2007The story of M
I was prescribed Effexor XR for low energy levels in November last year. At the time I became anxious when the dosage was increased from 75mg to 150mg. I was not warned of any possible effects of increasing the dosage. At this point I was then prescribed Solian (an antipsychotic which my psychologist said made some of her clients feel "euphoric") for anxiety and "ego disintegration" - which in retrospect was at the exact time the Effexor was ramped up. I was not told of possible weight gain. The pdoc seemed to think a possible diagnosis was Generalised Anxiety Disorder. I found the 150 Effexor started to make me feel jittery and interfered with my sleep (I was waking about 6am and I am not a morning person and normally sleep for longer). I asked that the dosage be lowered, but at that time in South Africa you could only get a 150 or 75mg capsule (tablets not available, but now have Venlor generic 37,5mg capsule here). I was then prescribed Trazadone for sleep. I was not told it was an antidepressant and occasionally if I did not take one, I would feel absolutely awful the next day - eventually made the connection and the pharmacy then told me it had to be taken every day. At this stage the psychologist (in March) said I seemed to have stabilised and it was my decision whether or not to continue with therapy. I was stupidly flattered that I was considered "ok", but opted to continue as I knew we had not even touched on very serious issues. Started to put on weight very quickly - 6kg's in two weeks. Mentioned this to psychologist who then said it might be the Solian and I could just stop it if I wanted to, which I did. I would never have touched it if I had known as I struggle with weight as an issue anyway. Went to pdoc at the end of April 2005 and told her re weight gain and complete loss of libido etc. She then decided to drop the Effexor XR from 150 mg to 75 mg in one day. She stopped the Trazadone cold turkey. Then I was to take 75 mg Effexor for 5 days while starting Zoloft. She also put me onto 10mg of Ambien and gave me Alprazolam (a benzodiazepine) "in case I felt a bit wobbly". About 6 days into this change-over I started to experience fevers, confusion, indecision, excruciating anxiety, nausea, dry retching, chills and a host of other things I cannot even remember. When I called the pdoc to say that I was feeling irrational, she said to me that the psychologist thought that "we should add in something else" - meaning a mood stabiliser. At this stage I actually couldn't believe her response and refused to take this. I continued to see the psychologist, hoping for some direction. She then began to say maybe I had "subtle hints or tendencies" of Bipolar 2. I said that I had never been hypomanic (although did feel revved up for a few days when Effexor upped to 150mg) and her response was that one does not have to have all the symptoms to have the condition. Needless to say, being in the middle of a hellish withdrawal and then being told that it could be an incurable condition with very serious implications made matters even worse for me in terms of anxiety (as I know it has serious implications in terms of further depressions, postpartum depression, etc). She did not seem to understand why her saying this would upset me and said that if I took Topamax (a migraine medication) I could lose up to 6 kg's! I then asked how sure she was of what she was saying to me and she said that a whole host of other things had to be ruled out, but because the Effexor had made me jittery, the Solian had not helped my anxiety and some other things made her wonder about it as a possible diagnosis. I then asked why no blood tests had been done at any stage and she became very defensive. I continued to suffer and tried to see another pdoc who said I seemed to "be in a tizz" and who just did not get it at all. After 2 weeks of utter hell, I then contacted a therapist that I used to see in Johannesburg (who I saw for almost a year after my breakup and who laughed at the Bipolar 2 question, saying he had never seen any evidence of it while I was seeing him) and via a contact of his I was advised to drop the Zoloft and go back onto 75 mg Effexor. At this point I felt as if I might die and the half dosage did alleviate the intensity of the symptoms to a degree. I now realise that I should have been put back onto a full dose and then tapered, but no-one even mentioned this to me. I then tried to carry on with my life for May and June, but felt very, very ill and anxious like I never have before. I continued to vomit nearly every day and thought I was going crazy (also went through alcohol and caffeine withdrawal as I could not even stand the smell). Typed "effexor hell" into the Net and then realised that I was not the only one going through this. My psychologist said I was "lucky" that we knew it was withdrawal (I told her!) because otherwise it could be mistaken for a "psychotic break" - even though none of the symptoms was of a psychotic nature. I was so worn out from being ill and not receiving proper help - at this point I could hardly even drink water - I went to a homeopath who tried to wean me off the Effexor (by then the generic capsule 37,5 was available here and my boyfriend and I began counting granules out etc). I eventually began to feel what I now realise is real depression. The anxiety was so bad that my boyfriend said it looked as if I was being put into boiling oil. Eventually by the end of June I broke down physically and mentally and could not function. For the first time in my life I felt death near me (I'm 36). I felt so awful I no longer wanted to be on this planet to experience that level of suffering. Eventually went to a clinic, where they used Prozac and a fistful of benzos and seroquel (a “mood stabiliser”) to wean me. I won't even go into how inept they were. Pdoc there said that I was having a major depressive disorder and that I had "obsessive tendencies" about medication (Duh...) - I kept asking them to reduce the number of benzos as I did not want to end up with another addiction. He said I should take Prozac for at least 2 and 1/2 years, possibly for the rest of my life. He said he could see no evidence of Bipolar, but that didn't mean I wasn't... I was still in a shocking state, but knew I could not stay in that awful place - they made me do group therapy (really patronising stuff) - etc - at a stage when I could hardly walk. At the moment I am taking 20 mg of Prozac, the Alprazolam was changed about two months ago to 20 mg Clobazam. I have weaned off the Ambien and Seroquel. I am still very anxious, very sensitive to noise - can't watch TV etc. Have become pretty much housebound + agoraphobic, which I hate, and which was never an issue for me before medication. All this has affected my relationship with my boyfriend, my career has ground to a halt and I missed my beloved Grandmother's 80th birthday (she has a benign brain tumour) because I was too ill to travel etc etc. I went through an unintentional Rivotril withdrawal in 2002, so have some inkling of a benzo withdrawal. I was also on Effexor and Ambien then and weaned myself over a longer period without problems (was after the very messy breakup of a 16 year relationship). Am absolutely petrified and do not feel like the same person at all. I am very worried about permanent damage. I am also very worried about the depression and anxiety re-emerging. I did have some mild depression and anxiety on certain occasions before this episode and very big trust issues etc (previous times when I was grieving a loss of in 1999 and even the breakup in 2002 I now see as sadness and grief and not real depression). I am sorry this is so long, but I am not able to summarise as well as usual and so much has happened. | |
Posted by Linda, 08:15 1 May 2007The Sunday Independent (Ireland)
The drugs don't work, warn top psychiatrists TOM PRENDEVILLE A DAMNING indictment by the country's most eminent psychiatrists paints a picture of patients' lives being needlessly put at risk by a cocktail of dangerous drugs, and a profession which is in the back pocket of vested interests in the pharmaceutical industry. "The psychiatric world has to be cleaned up - it's appalling. There are over 200,000 people on over-the-counter tranquilliser drugs," says Dr Michael Corry, a consultant psychiatrist. "In Ireland, there are 25,000 people on Zyprexa and 20,000 people on Seroxat. With Seroxat, there is a one-in-500 suicide risk. They get totally overwhelmed by a sense of disinhibition, and they literally feel they can't go on, and they kill themselves." Coincidentally, a damning Oireachtas report on the adverse side effects of pharmaceuticals, which was released last week, has come to more or less the same conclusions. The report stated that "the influence of the pharmaceutical industry is unhealthy". It also called into question the relationship between the pharmaceutical companies and psychiatric doctors, who are financially rewarded in the form of payments for ghostwriting medical-research reports, get free travel, research grants and numerous other perks. The all-party committee report also took a swipe at the widespread prescribing of psychiatric drugs. "Their use in therapy represents unwarranted medical intervention in what are often normal emotional difficulties," said. "The side effects include behavioural disorders, physical illness, dependence and even suicide." The report went on to say that some of the drugs "were of doubtful benefit" and that "where side effects are well known, they seem not to be appreciated or are ignored by prescribers". The Oireachtas Committee is now calling for the setting up of a Patient Safety Agency. Other senior doctors raise the issue of the use of drugs such as Clozaril, a widely used schizophrenia drug which can produce a litany of life-threatening reactions. "It's a very dangerous drug - and it's not the only one," said Dr Corry, who runs the Dun Laoghaire-based Institute of Psychosocial Medicine. "It's an absolute scandal that the Medicines Board has licensed these drugs - surely they can unlicense them, seeing as we have clear irrefutable evidence they are dangerous?" Professor Pat Bracken, consultant psychiatrist and clinical director of the West Cork Mental Health Service, says that many of the woes befalling psychiatry can be directly traced to the vast influence which the pharmaceutical industry now wields over the academic faculties that teach psychiatry - an influence gained through the doling out of vast research grants. "There are growing concerns about the way in which the pharmaceutical industry has come to dominate psychiatry," he warns. "The profession should be independent and be seen to be independent. And if it is not, it is a concern for everyone." | |
Posted by Linda, 13:16 1 June 2007AUTHOR, AUTHOR: Drug companies keep the real researchers under wraps
Medical trials are a vital part of drug marketing. With a positive result, the manufacturer can press even harder to get the drug more widely prescribed. The results also get plastered across advertisements in medical journals, so reinforcing the idea that the drug is both safe and effective. But the trial has also to be seen to be independent if it's to have any credibility. Unfortunately, most trials are funded by the drug company, and they are prepared and written by the company's employees. Under recent disclosure regulations, there's not much the drug company can do to hide the funding source - even though it reveals it in the smallest type possible - but there's plenty it can do to hide the authors. It's common practice to recruit a 'name' - usually a professor at a medical school - who takes full credit for preparing the study, even though he probably hasn't even bothered to read it. Meanwhile, the true authors slip back into their corporate obscurity. In a recent review of 44 medical trials published in 1994 or 1995, 33 were 'ghosted' - in other words, the true authors were never revealed. And, to a man, they worked for the drug company who would benefit from the favourable study. (Source: PloS Medicine, 2007;4:e19). | |
Posted by Linda, 11:54 3 June 2007June 3, 2007
After Sanctions, Doctors Get Drug Company Pay By GARDINER HARRIS and JANET ROBERTS A decade ago the Minnesota Board of Medical Practice accused Dr. Faruk Abuzzahab of a "reckless, if not willful, disregard" for the welfare of 46 patients, 5 of whom died in his care or shortly afterward. The board suspended his license for seven months and restricted it for two years after that. But Dr. Abuzzahab, a Minneapolis psychiatrist, is still overseeing the testing of drugs on patients and is being paid by pharmaceutical companies for the work. At least a dozen have paid him for research or marketing since he was disciplined. Medical ethicists have long argued that doctors who give experimental medicines should be chosen with care. Indeed, the drug industry's own guidelines for clinical trials state, "Investigators are selected based on qualifications, training, research or clinical expertise in relevant fields." Yet Dr. Abuzzahab is far from the only doctor to have been disciplined or criticized by a medical board but later paid by drug makers. An analysis of state records by The New York Times found more than 100 such doctors in Minnesota, at least two with criminal fraud convictions. While Minnesota is the only state to make its records publicly available, the problem, experts say, is national. One of Dr. Abuzzahab's patients was David Olson, whom the psychiatrist tried repeatedly to recruit for clinical trials. Drug makers paid Dr. Abuzzahab thousands of dollars for every patient he recruited. In July 1997, when Mr. Olson again refused to be a test subject, Dr. Abuzzahab discharged him from the hospital even though he was suicidal, records show. Mr. Olson committed suicide two weeks later. In its disciplinary action against Dr. Abuzzahab, the state medical board referred to Mr. Olson as Patient No. 46. "Dr. Abuzzahab failed to appreciate the risks of taking Patient No. 46 off Clozaril, failed to respond appropriately to the patient's rapid deterioration and virtually ignored this patient's suicidality," the board found. In an interview, Dr. Abuzzahab dismissed the findings as "without heft" and said drug makers were aware of his record. He said he had helped study many of the most popular drugs in psychiatry, including Paxil, Prozac, Risperdal, Seroquel, Zoloft and Zyprexa. The Times's examination of Minnesota's trove of records on drug company payments to doctors found that from 1997 to 2005, at least 103 doctors who had been disciplined or criticized by the state medical board received a total of $1.7 million from drug makers. The median payment over that period was $1,250; the largest was $479,000. The sanctions by the board ranged from reprimands to demands for retraining to suspension of licenses. Of those 103 doctors, 39 had been penalized for inappropriate prescribing practices, 21 for substance abuse, 12 for substandard care and 3 for mismanagement of drug studies. A few cases received national news media coverage, but drug makers hired the doctors anyway. The Times included in its analysis any doctor who received drug company payments within 10 years of being under medical board sanction. At least 38 doctors received a combined $140,000 while they were still under sanction. Dr. Abuzzahab received more than $55,000 from 1997 to 2005. Drug makers refused to comment, said they relied on doctors to report disciplinary or criminal cases, or said they were considering changing their hiring systems. Asked about the Minnesota analysis, the deputy commissioner and chief medical officer of the Food and Drug Administration, Dr. Janet Woodcock, said the federal government needed to overhaul regulations governing clinical trials and the doctors who oversaw them. "We recognize that we need to modernize the F.D.A. approach in keeping people safe in clinical trials," Dr. Woodcock said. Drug makers are not required to inform the agency when they discover that investigators are falsifying data, and indeed some have failed to do so in the past. The F.D.A. plans to require such disclosures, Dr. Woodcock said. The agency inspects at most 1 percent of all clinical trials, she said. Karl Uhlendorf, a spokesman for the Pharmaceutical Research and Manufacturers of America, said the trade group would not comment on The Times's findings. The records most likely understate the extent of the problem because they are incomplete. And the Minnesota Board of Medical Practice disciplines a smaller share of the state's doctors than almost any other medical board in the country, according to rankings by Public Citizen, an advocacy group based in Washington. Dr. David Rothman, president of the Institute on Medicine as a Profession at Columbia University, said the Times analysis revealed a national problem. "There's no reason to think Minnesota is unique," Dr. Rothman said. "Clinical trial investigators must be culled from only the finest physicians in the country," he said, "since they work on the frontiers of new knowledge. That drug makers are scraping the bottom of the medical barrel is an outrage." Payments by drug companies to doctors, whether or not the doctors have been disciplined, are a matter of much debate. Drug makers and doctors say the money finances vital research and helps educate doctors about helpful medicines. But others in the medical profession say the payments are thinly disguised incentives for doctors to prescribe more, and more expensive, drugs. Among the other doctors who were disciplined or criticized by the board and paid by pharmaceutical companies: ¶Dr. Barry Garfinkel, a child psychiatrist from Minneapolis who was convicted in federal court in 1993 of fraud involving a study for Ciba-Geigy. His criminal case made headlines across the state. From 2002 to 2004, Eli Lilly paid him more than $5,500 in honoraria, according to state records. Dr. Garfinkel said in an interview that he had wondered why drug makers would hire him as a speaker considering his statewide notoriety. He decided that "they're hiring me to influence my prescribing habits," so he quit giving sponsored talks and taking money from drug makers, he said. ¶Dr. John Simon, a Minneapolis psychiatrist who for years shared an office with Dr. Abuzzahab and was told by the state medical board in 1994 to complete a clinical training program after it concluded in a report that he "frequently makes abrupt and drastic changes in type and dosage of medication which seem erratic, not well considered and poorly integrated with nonmedication strategies." He prescribed addictive drugs to addicts and failed to stop giving medicines to patients suffering severe drug side effects, the board concluded. Dr. Simon earned more than $350,000 from five drug makers from 1998 to 2005 for consulting and giving drug marketing talks. Of this, Eli Lilly paid more than $314,000. Dr. Simon said in an interview that the board's action was a learning experience, and that drug makers continued to hire him to speak because "I am respected by my peers." Asked about Drs. Garfinkel and Simon, Phil Belt, a spokesman for Eli Lilly, said that both doctors were licensed to practice medicine and that the company relied on doctors to report disciplinary actions or criminal convictions against them. ¶Dr. Ronald Hardrict, a psychiatrist from Minneapolis who pleaded guilty in 2003 to Medicaid fraud. In 2004 and 2005, he collected more than $63,000 in marketing payments from seven drug makers. In an interview, Dr. Hardrict said it was "insulting" and "ridiculous" to suggest that income from drug makers might influence doctors' prescribing habits. "I bought the Mercedes because it has air bags, and I use Risperdal because it works," Dr. Hardrict said, referring to an antipsychotic medicine for schizophrenia. Johnson & Johnson, the maker of Risperdal, paid Dr. Hardrict more than $30,000 in 2003 and 2004. Srikant Ramaswami, a spokesman for Johnson & Johnson, said the company removed Dr. Hardrict as a speaker in 2004 when, as a result of his conviction, his name appeared in a government database. Asked why other drug makers continue to hire him despite a fraud conviction, Dr. Hardrict responded with an e-mail message stating only, "I will pray for you daily." In cases involving Dr. Abuzzahab over 15 years in the 1980s and '90s, the medical board found that he repeatedly prescribed narcotics and other controlled substances to addicts, renewing one patient's prescriptions six weeks after the patient was jailed and telling another that his addictive pills should be thought of as "Hamburger Helper." He prescribed narcotics to pregnant patients, one of whom prematurely delivered a baby who soon died. In explaining his abrupt discharge of the suicidal Mr. Olson, Dr. Abuzzahab told the medical board that "if a patient is determined to kill himself, he can't be prevented from doing it and hospitalization postpones the event," records show. Mr. Olson's sister, Susie Olson, said Dr. Abuzzahab "had no time for my brother unless David agreed to get into a drug study. He said, 'You're wasting my time and the hospital's.' It was all about money." Separately, the F.D.A. in 1979 and 1984 concluded that Dr. Abuzzahab had violated the protocols of every study he led that they audited, and reported inaccurate data to drug makers. He routinely oversaw four to eight drug trials simultaneously, often moved patients from one study to another, sometimes gave experimental medicines to patients at their first consultation, and once hospitalized a patient for the sole purpose of enrolling him in a study, the F.D.A. found. Dr. Abuzzahab, 74, was president of the Minnesota Psychiatric Society and two decades ago was chairman of its continuing education and ethics committees. He would not discuss the specifics of his disciplinary record, saying he did not have the time. But in 1998 he signed an agreement with the board saying that his conduct "constitutes a reasonable basis in law and fact to justify the disciplinary action." A simple Google search reveals Dr. Abuzzahab's 1998 medical board disciplinary file, which was reported at the time by a local newspaper and a TV station. In 1998, The Boston Globe featured Dr. Abuzzahab in a front-page article questioning the safety of psychiatric drug experiments. And in 1999, the NBC program "Dateline" did a segment about a woman who committed suicide while in a drug experiment he supervised. In June 2006, the medical board criticized Dr. Abuzzahab, this time for writing narcotics prescriptions for patients he knew were using false names, a violation of federal narcotics laws. Despite all this, drug makers continued to hire him. Dr. Abuzzahab's résumé lists 11 publications or research presentations since 2000, when the medical board lifted its restrictions on his license. Takeda, a Japanese drug maker, confirmed that Dr. Abuzzahab was doing a study financed by the company on its sleep medicine, Rozerem. Eisai, another Japanese drug maker, said that although Dr. Abuzzahab had signed a clinical trial agreement with the company to study its Alzheimer's drug, Aricept, it told him two days after a reporter asked for comment on the case that he was not qualified to be an investigator. And at AstraZeneca, for which Dr. Abuzzahab said he had performed clinical trials and still gave drug marketing lectures, a spokesman said the company was "concerned" about Dr. Abuzzahab's disciplinary record. "We have our own internal processes for dealing with these matters, which are under way," said Jim Minnick, an AstraZeneca spokesman. The Minnesota records often fail to distinguish between drug company payments to doctors for research and for marketing, so it is sometimes impossible to determine why doctors were paid. Some doctors, like Dr. Abuzzahab, clearly performed both research and marketing. Gene Carbona, who left Merck on good terms in 2001 as a regional sales manager after 12 years in drug sales, said the only thing the company considered when hiring doctors to give marketing lectures was "the volume or potential volume of prescribing that doctor could do." A Merck spokesman declined to comment. Mr. Carbona, now executive director of sales for The Medical Letter, which reviews drugs, said that had he known that a doctor had a disciplinary record for excessive prescribing, "I would have been more inclined to use them as a speaker." | |
Posted by Linda, 09:55 15 June 2007http://www.apa.org/ed/neuro.html
Treating Mental Disorders A Neuroscientist Says No to Drugs By JOSHUA ROLNICK Elliot S. Valenstein has spent most of his career searching for biological explanations for behavior. Now, after more than 40 years, he is attacking the prevailing biochemical explanations for mental illness. "We have almost reached the point where there will be no limits to what people will believe brain chemistry can explain," he writes in the introduction to his new book, Blaming the Brain: The Truth About Drugs and Mental Health (The Free Press). It's time to stop blaming mental disorders on brain chemistry, he argues. In simple terms, the biochemical theory holds that clinical depression, schizophrenia, and other disorders result mainly from chemical imbalances in the brain. Drugs like Prozac and lithium are supposed to work because they correct such imbalances. In his book, however, Mr. Valenstein, an emeritus professor of psychology and neuroscience at the University of Michigan, argues that scientifically, the biochemical explanation of mental illness rests on shaky ground. Environmental and cognitive variables are as important as biology, he writes, and psychotherapy is often just as effective as drug treatments, which pharmaceutical companies, psychiatrists, and others have successfully promoted. Mr. Valenstein, a former chairman of Michigan's biopsychology program, seems an unlikely crusader. In his years of research on rats and other laboratory animals, and in more than 140 scholarly articles, he studied how the brain and other biological factors, such as hormones, influence behavior. In the latter part of his career, the psychologist grew more interested in the history of his field -- a history he has not always praised. In Great And Desperate Cures (Basic Books, 1986), he argued that scant scientific evidence supported the use of lobotomy to treat certain mental disorders, even though doctors and the public embraced the procedure in the 1940s. When Mr. Valenstein began his new book three years ago, he planned to write a history of brain-chemistry theory, not a critique. "I used to lecture to students and put together a reasonably coherent story," he says. "I knew there were gaps, but this was an emerging science." By the time he was halfway through writing the book, however, his skepticism had become unshakable. "I began to feel that the evidence that didn't fit was becoming overwhelming." A combination of factors gave rise to the acceptance of drug treatments for schizophrenia and other mental disorders, he argues. Researchers sometimes stumbled upon the drugs inadvertently, he writes. For example, one drug that is rarely used now, chlorpromazine, originally a synthetic dye, was one of the first antipsychotic medications, after scientists concluded that it might help treat post-surgical shock. "With no effective treatment of mental illness," he writes, "almost anything that held out any hope was worth trying." As scientists learned more about the brain and its interaction with certain drugs, theories emerged to explain several major illnesses. Schizophrenia, for example, was believed to result from too much activity of dopamine, a neurotransmitter. The theory evolved when scientists discovered that, on the whole, the more an antipsychotic drug blocked the action of dopamine in the brain, the more the symptoms of schizophrenia were eased, Mr. Valenstein explains. But researchers have failed to find direct evidence that dopamine is, in fact, too active in the brains of schizophrenics, he says. And although most antipsychotic drugs did restrict dopamine activity after a few hours, he writes, they had no therapeutic benefit for the first few weeks of treatment. As a result, Mr. Valenstein writes, one study found that the drugs helped only about 60 per cent of schizophrenics. Similarly, he says, antidepressants appear to help only 30 to 40 per cent of patients. Mr. Valenstein argues not that drugs never work, but that they do not attack the real cause of a disorder. Biochemical theories, he argues, are an "unproven hypothesis" -- and probably a false one. The pre-eminence of drug treatments is no accident, he goes on. Pharmaceutical companies have a financial stake in their popularity, and promote them heavily among doctors and patients. Mr. Valenstein cites studies that examined some of the literature distributed by the companies and found that much of it contained misleading or unbalanced information. Drug companies are also the largest sponsor of medical research in the United States and Canada, Mr. Valenstein says. In some cases, they give complete freedom to researchers. In other cases, the contracts they require give them the right to exclude information from published reports, or to delay publication of the report itself. A spokesman for one company Mr. Valenstein criticizes, Eli Lilly and Company, declined to comment. Another, Pfizer Inc., did not respond to requests for comment. Psychiatrists, too, have supported the use of the drugs, he argues. For one thing, he says, an emphasis on medication allows psychiatrists to fend off competition from psychologists and social workers, who usually charge less for their services, but who cannot prescribe drugs. While that may not be the reason for their support, he writes, "there is little doubt that since the 1960s, psychiatry has increasingly emphasized biochemical factors as the cause of mental disorders." Paul H. Wender, a professor of psychiatry at the University of Utah, denies that psychiatrists favor drug treatments as a way to limit competition. "There have been 2,000 studies of the efficacy of psychotropic drugs in schizophrenia," says Dr. Wender, co-author of Understanding Depression, a book Mr. Valenstein criticizes. "To argue that psychiatry has a medical passion is untrue," agrees Donald F. Klein, Dr. Wender's co-author. Theories aside, he says, psychiatrists prescribe drugs because they work. Mr. Valenstein emphasizes that he does not intend to discourage patients from trying medication as one option. But he hopes that Blaming the Brain will open up a dialogue about the biochemical theory of mental illness, even as physicians feel increasing pressure to ignore other treatments, like psychotherapy, in favor of costly drugs that may have serious side effects and little benefit. Right now, he writes, "the theory is being pursued relentlessly on a path filled with many dangers." | |
Posted by Linda, 09:57 15 June 2007Active placebos versus antidepressants for depression (Cochrane Review)
Moncrieff J, Wessely S, Hardy R ABSTRACT A substantive amendment to this systematic review was last made on 27 July 1998. Cochrane reviews are regularly checked and updated if necessary. Background: Although there is a consensus that antidepressants are effective in depression, placebo effects are also thought to be substantial. Side effects of antidepressants may reveal the identity of medication to participants or investigators and thus may bias the results of conventional trials using inert placebos. Using an 'active' placebo which mimics some of the side effects of antidepressants may help to counteract this potential bias.Objectives: To investigate the efficacy of antidepressants when compared with 'active' placebos.Search strategy: The Cochrane Collaboration Depression, Anxiety and Neurosis review groups's search strategy was used to search MEDLINE (1966-2000), PsychLIT (1980-2000) and EMBASE (1974-2000) and this was last done in July 2000. Reference lists from relevant articles and textbooks were searched and 12 specialist journals were handsearched up to 1996.Selection criteria: Randomised and quasi randomised controlled trials comparing antidepressants with active placebos in people with depression.Data collection and analysis: Since many different outcome measures were used a standard measure of effect was calculated for each trial. A subgroup analysis of inpatient and outpatient trials was conducted. Two reviewers independently assessed whether each trial met inclusion criteria.Main results: Nine studies involving 751 participants were included. Two of them produced effect sizes which showed a consistent and statistically significant difference in favour of the active drug. Combining all studies produced a pooled estimate of effect of 0.39 standard deviations (confidence interval, 0.24 to 0.54) in favour of the antidepressant measured by improvement in mood. There was high heterogeneity due to one strongly positive trial. Sensitivity analysis omitting this trial reduced the pooled effect to 0.17 (0.00 to 0.34). The pooled effect for inpatient and outpatient trials was highly sensitive to decisions about which combination of data was included but inpatient trials produced the lowest effects.Reviewers' conclusions: The more conservative estimates from the present analysis found that differences between antidepressants and active placebos were small. This suggests that unblinding effects may inflate the efficacy of antidepressants in trials using inert placebos. Further research into unblinding is warranted. Citation: Moncrieff J, Wessely S, Hardy R. Active placebos versus antidepressants for depression (Cochrane Review). In: The Cochrane Library, Issue 1 2003. Oxford: Update Software. This is an abstract of a regularly updated, systematic review prepared and maintained by the Cochrane Collaboration. The full text of the review is available in The Cochrane Library | |
Posted by Linda, 11:08 15 June 2007Trends in the prescribing of antidepressant pharmacotherapy: office-based visits, 1990-1995. Sclar DA. et al. Clin Ther 1998 Jul-Aug;20(4):871-84; 870. The results of this study show that the number of office visits resulting in prescription of an antidepressant drug increased from 16,534,268 in 1990 to 28,664,796 in 1995, a 73.4% increase. A diagnosis of depression was documented in 6.7% of the U.S. population in 1990, and in 7.1% in 1995, a 16.4% increase. The large increase in number of prescriptions, not matched by a similar increase in the prevalence of depression, suggests that the criteria for prescribing antidepressant medications have loosened during the study period. A variation in rates of prescribing of different class of drugs was also noticed, with a decline in use of tricyclic antidepressants (from 42% to 25%), and an increase in use of selective serotonin reuptake inhibitors (from 37% to 65%). ________________________________________ Association between selective serotonin reuptake inhibitors & upper gastrointestinal bleeding population based case-control study. de Abajo, FJ, García Rodríguez LA, Montero D. BMJ 1999;319:1106-1109 ( 23 October ). The results of this study show that users of the antidepressants selective serotonin reuptake inhibitors (SSRIs) have a significantly increased risk of upper gastrointestinal (GI) bleeding, compared to nonusers. The study was conducted on 1651 patients hospitalized with upper GI bleeding, and 10,000 matched controls. Use of SSRIs was associated with a 3-fold increased risk of bleeding, compared to nonuse. The incidence of this complication was estimated at 1every 8,000 prescriptions. Combined use of SSRIs and aspirin was associated with a 7-fold increased risk of GI hemorrhage, and combined use of SSRIs and non-steroidal anti-inflammatory drugs resulted in a 15.6-fold increased risk. The authors emphasize that the large increase in risk of GI hemorrhage observed in their study could have important public health implications due to the frequent use of both classes of drugs in industrialized countries. ________________________________________ Hemorrhagic syndromes related to selective serotonin reuptake inhibitor (SSRI) antidepressants. Seven case reports and review of the literature. French. Nelva A, Guy C, Tardy-Poncet B, Beyens MN, Ratrema M, Benedetti C, Ollagnier M. Rev Med Interne 2000 Feb;21(2):152-60. The results of this study suggest that intake of the antidepressants selective serotonin reuptake inhibitors is associated with an increased risk of developing hemorrhagic syndromes. This adverse effect is under-recognized and under-reported, and may be due to a decrease in concentration of platelet serotonin, leading to platelet dysfunction. ________________________________________ Antidepressant Medication Use and Breast Cancer Risk. Cotterchio M, Kreiger N, Darlington G, and Steingart A. Am J Epidemiol 2000;151:951-57. The results of this study indicate that women who take antidepressants are at significantly higher risk of developing breast cancer, compared to the general population. The association between antidepressant drugs and breast cancer first emerged from animal and epidemiological data. This case-control study, conducted to further test the hypothesis, found that users of selective serotonin reuptake inhibitors (SSRIs) and tryciclic antidepressants have a 7- and 2-fold increased risk of breast cancer, respectively, compared to nonusers. The finding of a large increase in risk of breast cancer in users of SSRIs may have public health implications owing to the high prevalence of use of this class of drugs. ________________________________________ Comparative study of fluoxetine, sibutramine, sertraline and dexfenfluramine on the morphology of serotoner |







