4/19/2001 – April Edition of ICFDA now Online

Twenty-three new articles from the past month have just been
selected from newspapers across the country and posted our
ICFDA site at http://www.drugawareness.org.

Included among them are two articles that offer proof there are
safer ways to treat depression then by taking pills. One is from
Newsweek entitled “Nourishing Your Brain,” which discusses
studies showing that fats in fish and walnuts can ward off
depression. Another from Reuters showing how aerobic
exercise effectively treats depression.

You will also want to read how a world-renowned scientist saw
his job offer evaporate after he warned that the popular
antidepressant Prozac might trigger suicide. The manufacturer
is an important donor to a mental health institute associated with
the university who courted the doctor. Read “Prozac Critic Sees U
of T Job Revoked.”

Have you seen the ads for Serafem?—the new “cure” for PMDD,
a mental disorder that has yet to be proven to exist? Careful, it’s
just repackaged Prozac in pretty, new pink coating. Be sure to
read the riveting expose by Kelly O’Meara entitled “Misleading
Medicince.”

Plus, there’s new information on Viagra, Rezulin, Accutane, MMR
vaccinations and more.

Mark

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One Celexa Killed my Father

“He was not a depressed man, nor would he ever have taken his own life.”

 

My father had been suffering numbness in his arms and legs for about a year and it was getting progressively worse. After visiting numerous doctors and having all kinds of tests, he was finally told that he had spurs on his spinal cord and that surgery could remove them.

Of course he was told there was a risk of paralysis, but that is true of any back surgery. He had some discs removed from his back thirty years ago and came out of that fine.

My father was always a very active man, but lately he just didn’t feel well enough to pursuit his usual interests. Any way, on January 24, I took him to the doctor and my father told me he was going to ask for some antidepressants.

I told him not to because of the side effects.

He came out of the exam room with a box of 56 Celexa and said the doctor told him these were a milder antidepressant and did not have the side effects that most have.

I took my dad home and later that evening, one of my brothers visited my dad. He said my dad had taken one of the Celexa and was crawling out of his skin and speeding.

On January 25, my father shot and killed himself.

After reading the package insert for Celexa, I discovered that they consider depression as having at least five of nine symptoms listed. My father only had three. I feel the doctor should never have given my father these drugs. He was not a depressed man, nor would he ever have taken his own life. He was looking forward to this surgery. He was only in a depressed mood because he could not get out to go dancing or do the other things he liked to do.

 

3/18/2001

This is Survivor Story number 9.
Total number of stories in current database is 34

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Hope through alternatives even after long-term use of Prozac

 

“The doctors said that I needed the drugs to pull through. I finally said, ‘No more drugs!'”

 

My name is Tammy.

I was diagnosed with bipolar depression about seven years ago. I have been in and out of the mental ward three times in the seven years.

This may be kind of long, but I feel that it is very important for those who have this condition. I would like to let you know that there is away to heal from this, other than the use of drugs.

I was under doctors’ care with the use of drugs — lithium, Prozac etc. These drugs did nothing for me. I still sheltered myself from life outside the home. Was afraid to speak to anyone about what I was going through. I slept all the time, had nothing that interested me at all, just sat and watched TV. If I slept, then nothing could go wrong and I would not have to face reality.

I had to give my children to the state foster care system. This was the hardest thing I ever had to do. My children where very young and did not understand why we where not together. We told them what I was going through, but at the age they where they did not understand. I still managed to visit with them when I was allowed to. I cried when I left them, for they were in different homes. This made me feel even more alone.

I would cry sometimes all day and for no reason. I had no control. Was unable to do my job at work so they let me go. Now, no job no children. I had to move back to my parents’ home. A home of nothing but abuse.

The doctors said that I needed the drugs to pull through. I finally said, “No more drugs! They are not doing me any good.” So I took myself off all drugs. The doctor said that she would not recommend me doing that but she could not make me take them. I have managed to deal with this for years. No friends, no family, no fun.

Till I met Bev. I met her at a very tiring time in my life. My mother was diagnosed with (cholangio Carcinowa), Bio-duct cancer. Grandfather had died a month before my mother. I was a mess. Went to work and all anyone had to say was “Hi, how are you?” and I would fall all apart.

This gal Bev saw that I was not alright, so she began giving me some of the Young Living Essential Oil supplements (mentioned in Dr. Tracy’s book and tape on withdrawal and rebuilding). I took them and she would come around later and asked me how I felt. I did feel better but was not sure if the supplements were the reason why I could work.

Bev took me to a massage therapist and I had an emotional release done. Boy, after that was done I did not think that it worked. As we left I told Bev get me home — I really needed to get home. Not sure why I had to get there but just get me home. I had a business appointment right when I got home. I called and canceled it, felt that I could not do it right then.

A few hours passed and I was at home when I started to have a large crying spell. I cried so hard that I had dry heaves. I could not keep anything down and could not sleep. Could not sit still, this went on all day and night. Called Bev to tell her I was afraid and what I was going through. The next day I felt as though nothing at all happened to me. I was better than fine, I was happy and could not wait to go somewhere. My concentration improved, I got out doing things again.

Bev helped me with my diet, supplements, the essential oils, etc. This is what I feel saved my life. This was my last chance, for I had tried everything and nothing worked. But the Young Living Essential Oils products worked!

I have a ways to go but feel that Young living will see me through all the changes. I hope that this will help other people to believe that there is something out there that will work and without drugs. I am stronger than I ever have been and I owe it all to Young Living Essential Oils.

Thank you, Bev and Young Living, from the bottom of my heart! You saved me!!!!!!!!

Tammy

2/18/2001

This is Survivor Story number 1.
Total number of stories in current database is 34

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17-Year Old Friend Committed Suicice on Prozac

It killed one of my friends and almost killed another. I can’t believe that it is still on the market…”

 

I am writing this because I think people need to hear my friend’s story.

One of my close friends was put on Prozac. She was 17. Over the summer I spent a lot of time with her. She appeared happy and never seemed to let anything bother. I did find it strange that when I asked if she ever had anything bothering her she always seemed to change the subject back to my problems. Little did I know that she let all those problems bottle up inside of her. My friend committed suicide August 31, 1999, at the age of 17.

I know that she had other problems, she did share a few, but I think that Prozac also had something to do with her actions. I never knew what the drug did to people until I began researching it for a paper for my senior English class. Another one of my friends was also placed on Prozac for depression after our friend died. In December of 1999 she too almost committed suicide. She had all the letters written out but a phone call from a friend stopped her. She told me that while she was on the drug she felt like no one understood how she felt. She said that she felt like she was in her own world and no one understood how she was feeling. This feeling of solitude brought her great pain and she had convinced herself that the only way to end the pain was to kill herself.

I am very grateful to that person who called her right before she did it. Somehow the phone call snapped her into reality and she realized that she didn’t want to kill herself, all she wanted was for the pain to stop. Something has to be done about this drug. It killed one of my friends and almost killed another. I can’t believe that it is still on the market and I don’t personally believe that it should be. I know the pain that comes when a friend commits suicide. I wouldn’t wish that feeling on anyone and I believe that if this drug continues to be prescribed this world is going to experience many more self-induced death.

I needed to tell someone this. Thank you for your time and listening.

M

12/9/2000

This is Survivor Story number 4.
Total number of stories in current database is 96

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A Mindless Zombie on Paxil

“I was all jittery and I just felt weird.”

My name is Rachel. I had a bad experience with Paxil. I went to my
family doctor and told him about my depression. After talking to me for about 10 minutes, he decided that I needed Paxil for my depression. I was reluctant, but I took it. I took my first pill the next morning. At first I
felt nauseated. Later during the day, I was extremely happy and really hyper. I walked for miles and didnt get tired. The next morning I woke up craving the pill. But I didn’t take it. I was afraid. I was all jittery and I just felt weird. I don’t think this is a very effective drug unless you want to be a continously happy mindless zombie.

Rachel

10/12/2000

This is Survivor Story number 9.
Total number of stories in current database is 96

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Prozac prescribed for Chronic Fatigue Syndrome

“It was, by far, the most terrifying experience of my life; I literally felt like I was losing my mind, being taken over by an alien force.”

 

To make an excruciatingly long story tolerably short, I was given Prozac for Chronic Fatigue syndrome by my GP. I was on it for a year with no major problems, in fact I quite liked the unsought-for increase in confidence, sociability, etc.

After stopping, I began experiencing a whole host of ‘mental problems’ that I’d never had before. This began as a strange and almost indescribable difference in perception; it was as if I saw things without any emotional response. Even the simple, everyday things — looking at a tree, a dog, being in a roomful of people listening to conversation – took on a bizarre, otherworldly aspect. It was as if I were on some kind of anesthetic while still awake. This escalated over a period of several months until it took on the form of full-blown depersonalization disorder. At the same time, I began experiencing episodes of derealization and extreme LSD-like experiences, a constant experience of mental impairment, and severe loss of short-term memory. My doctor said he’d never heard of such a thing and referred me to a psychiatrist, who proceeded to tell me that this wasn’t caused by the drug, but that my ‘illness’ had gotten worse. ‘What illness,’ quoth I. ‘Your depression,’ quoth he. When I told him that never had depression, just fatigue and food allergies, and I’d certainly never had any of these extreme forms of mental illness before or anything remotely like them, he looked at me blankly for a minute, and then somehow convinced me that they had just ‘happened,’ that my condition had just coincidentally deteriorated, that I’d always ‘really been depressed’ and just hadn’t known it, and that what I needed to do to make these things go away was to go back on the drug. I was in desperate straits, scared out of my wits and appeared to have no other options. I did as he said, re-started Prozac. All the symptoms immediately got worse. I was having constant, unremitting LSD-like experiences, horrible, nauseatingly violent dreams, a constant state of unremitting depersonalization and derealization to the point where I could barely function. It was, by far, the most terrifying experience of my life; I literally felt like I was losing my mind, being taken over by an alien force.

I went to several other psychiatrists to try to find an ‘expert’ who could explain all of this. Dr. Daniel Aurbach (quoted in a recent story in Newsweek as a Prozac authority) told me that he’d never heard of Prozac causing any of these phenomena, that I should not worry, it was ‘a very safe drug.’ Dr. Deborah Nadel of UCLA told me that she’d ‘bet money’ that this had nothing to do with Prozac, that I should increase the dose, and that I needed to take Klonopin for my ‘anxiety,’ and go into therapy, which I did for several weeks. Eventually, I could no longer bear the asininity of sitting in a room talking to this woman about my childhood while tripping my brains out on a drug, hallucinating and having out-of-the-body experiences, nauseatingly violent dreams (when I was even able to sleep) and not being able to remember what I did yesterday. I expressed my concerns to Dr. Nadel about the approach we were taking; she told me that I should take a neuroleptic (anti-psychotic medication). To my eternal credit, I did not throw her out the window, but, patient guy that I am, went to a few more shrinks. They all told me basically the same things:

Prozac doesn’t do this, you must have ‘already’ been mentally disturbed (or this just ‘happened,’ nothing to do with the drug), all reports of adverse effects from Prozac were started by the Scientologists, why don’t you try a neuroleptic, they’re safe in small doses, etc. etc. etc. One morning, after waking up in sheer terror from a particularly horrible dream in which men in masks were ripping first the eye-balls and then the brains out of two young girls, I went into the bathroom and sat on the toilet, letting the water in the sink run to give me something other than my mind to listen to. ‘Jesus,’ I thought, ‘what the *hell* could a dream like that possibly mean? What is happening to me?’ ‘It doesn’t matter,’ said a clear, calm voice in my mind, ‘because I’m going to kill myself.’

In that moment, I realized that I didn’t give a rat’s ass what any psychiatrist said. I was stopping this shit no matter what. I’d walked into this with a mild case of fatigue and some food allergies, and now I’m sitting here on the edge of psychosis with a voice telling me to off myself. I don’t think so.

I went to a doctor I’d seen several years before, Dr. Murray Susser, one of the foremost authorities on the treatment of Chronic Fatigue Syndrome and related disorders. I knew that he had prescribed anti-depressant medications (I’d read his book), and I also knew him to be a knowledgeable, widely educated, intelligent and decent man. I told him my story. When I got to the part about everybody telling me that it ‘couldn’t be the drug,’ he looked up from his notes and said “Bullshit! It’s the drug. I see this kind of thing all the time. I don’t know how these psychiatrists can be in such denial, the literature is full of reactions like this.” We talked for a long time, figuring out a workable program for safely tapering off the drug, and for trying to get myself back in shape afterward. I left his office feeling hope for the first time in eight months.

Happily, right at that time, I found the book ‘Prozac: Panacea or Pandora?’ by Ann Blake Tracy, which I promptly read. It was like the light at the end of the tunnel; this book described everything that had happened to me in great detail, gave scientific reasons why it happened, backed it all up with solid research, included testimonials from hundreds of others in the same situation, and even gave me some insight as to how seven of the top psychiatrists in LA could be so amazingly, criminally inept.

I thought about suing them. For about thirty seconds. How could I prove what this stuff has done to me? For me, the most frightening aspect of this whole adventure, even more so than journeying to the brink of insanity, is the realization that these psychiatrists have all this power and authority to proclaim what is and isn’t real as regards your own mental function and sense of self, whether they have any real idea what they’re talking about or not. [I’ve learned that] SSRI’s can, in fact, cause LSD-like experiences, due to their artificial raising of 5HT (the chemical that LSD achieves its effect by mimicking). However, it’s not ‘fun, trippy acid’ kind of stuff. It’s more like LSD mixed with PCP mixed with anesthesia, mixed with Sulfur from the Pits of Hell, and like the energizer bunny, it keeps going and going and going…

As for depersonalization disorder (something the docs all told me Prozac couldn’t be the cause of): it’s listed right on the package insert as a possible side-effect. Too bad none of these guys thought it worth-while to give to me. Or read…..I like to learn from my experiences. In searching for positive aspects to this whole thing, I can say I now have at least some idea what schizophrenia might be like. For whatever that’s worth.

 

Years 2000 and Prior

This is Survivor Story number 82.
Total number of stories in current database is 96

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5/23/2000 Accutane May Be Linked To Depression, Suicide

In case you missed this I wanted to send this out again. I feel it is very
important to know. There are too many children on this type of medication and
little knowledge of these serious side effects to this drug. How many
children are ending up on antidepressants as a result of their acne meds?

Ann Blake-Tracy
_______________________________

http://www.pslgroup.com/dg/5d8e2.htm

FDA Reports Accutane May Be Linked To Depression, Suicide

WASHINGTON, MD — February 26, 1998 — The United States Food and Drug
Administration is advising consumers and health care providers of new
safety information regarding the prescription anti-acne drug Accutane
(isotretinoin) and isolated reports of depression, psychosis and rarely
suicidal thoughts and actions.

Accutane was approved in 1982 to treat only a very special type of acne —
severe nodular acne that has not responded to other therapies.

Although the Accutane label already included information regarding
depression as a possible adverse reaction, the agency felt health care
providers and others needed additional information as a result of adverse
event reports the agency has received.

FDA and the drug manufacturer are strengthening this label warning, even
though it is difficult to identify the exact cause of these problems. Such
problems could already be more common among the patient populations likely
to be on the drug.

However, because some patients who reported depression also reported that
the depression subsided when they stopped taking the drug and came back
when they resumed taking it, the agency and the manufacturer felt the
strengthened labelling was warranted as a precautionary measure.

Given the complex nature of depression and suicidal conditions, the new
label information will advise health care providers that merely
discontinuing the drug may be insufficient to remedy these adverse events
and that further evaluation may be needed.

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4/16/2000 – More from Boston Globe on Drug Safety Issues

This story ran on page A10 of the Boston Globe on 5/15/2000.
© Copyright 2000 Globe Newspaper Company.

A BOSTON GLOBE EDITORIAL

Better drug reporting deal with a wide range of conditions, from depression
to osteoporosis, doctors are reaching increasingly for their prescription
pads. Patients who consume these drugs have faith that any side effects other
patients have had are carefully reported by physicians and monitored by
officials so that, if need be, warnings can be issued.

That faith is misplaced.

While the drug companies and the US Food and Drug Administration have a
system for maintaining an adverse-event database, doctors are not required to
report the serious problems patients have with a drug. As a result, there are
distinct limitations in the system to track bad reactions and then add new
warnings on the drug’s label or withdraw it altogether. Public Citizen, a
watchdog group in Washington, D.C., reports that actual surveys of medical
records turn up 10 times as many drug reactions as are reported voluntarily
by doctors.

Under current practices, drug companies are required to alert the FDA within
15 days of any severe reactions to drugs and within a year of less serious
reactions, but without more mandatory reporting by practitioners (hospitals
and nursing homes are required to make such reports), companies’ own
awareness of problems will be stalled.

If reporting by doctors of bad reactions were mandatory, both the FDA and Eli
Lilly and Co. would know more than they do about some of the problems
connected with Lilly’s popular antidepressant, Prozac. While Prozac and
similarly acting drugs have been hailed by both doctors and patients for
relieving symptoms that can often presage suicide, there have long been
reports of extreme agitation and anxiety among a small percentage of users.

One argument against mandated reporting of adverse reactions from doctors is
the extra paperwork this would entail. But, for the past several years, the
FDA has maintained a Web site that permits doctors – and patients – to make
online reports with little fuss. Closer monitoring could give both health
professionals and the public a greater awareness of what to be alert for as
they make use of the drugs that are changing American medicine.

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The Aftermath of Antidepressants

The Aftermath Of Prozac, Zoloft, Luvox, Fen-Phen, & Many Other Serotonergic Drugs

By Ann Blake-Tracy – Executive Director,
International Coalition For Drug Awareness

Ann Blake-Tracy has specialized for 10 years in adverse reactions to serotonergic medications. She is the executive director of the International Coalition for Drug Awareness (www.drugawareness.org) and author of the book PROZAC:PANACEA OR PANDORA?

WARNING: IT SHOULD BE NOTED THAT A GRADUAL TAPERING OFF OF MEDICATIONS IS SAFEST WITHDRAWAL METHOD TO AVOID SERIOUS WITHDRAWAL EFFECTS

Often there is the terrible withdrawal associated with the SSRIs. Unless patients are warned to come very slowly off these drugs by shaving minuscule amounts off their pills each day, as opposed to cutting them in half or taking a pill every other day, they can go into terrible withdrawal which is generally delayed several months. This withdrawal includes bouts of overwhelming depression, terrible insomnia and fatigue, and can include life-threatening physical effects, psychosis, or violent outbursts.

Note: Keep in mind that these drugs are all serotonergic agents and clones or “copy cat” drugs of Prozac – the first SSRI antidepressant introduced to the market in America. Basically what applies to one, applies to the others. For instance we have more data out on Prozac because it has been around longer, but as the mode of action is the same for all of these meds the effects will be the same for the other drugs on this list as it is for Prozac. If we are discussing one drug, similar effects would be expected from any other company’s version of the drug. In fact it would be more honest to give them the titles of Prozac #1, Prozac #2,Prozac #3, etc. rather than the brand names they have been given, from the second clone, Zoloft, to the latest Prozac clone, Celexa.

My concern is that each new SSRI introduced seems to be a little stronger on serotonin reuptake and therefore potentially more dangerous. And the all too common practice of going from one SSRI to another blocks additional receptors and magnifies the harmful effects of these medications. It is crucial to learn that according to medical research the theory behind this group of drugs is invalid. Known as serotonin reuptake inhibitors. They are designed to block serotonin in the brain, thereby increasing brain levels of this neurotransmitter. Yet for three decades researchers have been intensely interested in serotonin because LSD and PCP produce their psychedelic effects by mimicking serotonin. Elevated serotonin is found in: psychosis or schizophrenia, mood disorders, organic brain disease, mental retardation, autism and Alzheimer’s. While low levels of the metabolism of serotonin (which also produces high serotonin), are found in those with: depression, anxiety, suicide, violence, arson, substance abuse, insomnia, violent nightmares, impulsive behavior, reckless driving, exhibitionism, hostility, argumentative behavior, etc. The drugs increase serotonin and decrease the metabolism of serotonin leading to any and all of the above results. This information is extremely crucial for patients and physicians to learn as soon as possible. We have a high rate of use of these drugs nationwide. Raising serotonin and lowering the metabolism of serotonin in such a large number of people can produce very serious, widespread and long term problems for all of society.

So why are we now in the 90’s being told that increased serotonin is good for us? Is it because it is good for the pocketbooks of the manufacturers? One manufacturer is running full page newspaper and magazine ads and half hour TV infomercials to bring in over $7 million daily, while on the other hand they are settling Prozac suicide cases for huge amounts of money in exchange for silence from victim’s families on the details of those settlements. The silence in the court cases insures that the drug will be allowed to finish out its patent time, thus bringing in the highest possible profits for the company. They know that with $7 million coming in daily, they can afford to settle a large number of lawsuits and still come out “smelling like a rose” financially.

Eli Lilly has been sued for Prozac related deaths in numerous state and federal courts with most of these cases being settled or dismissed – many were dismissed due to the unethical manipulation of the Wesbecker verdict
(see time line for details).

We have witnessed no decrease in suicide, but increases in murder/suicide, suicide, unwed pregnancies, domestic violence, manic-depression, MS, hypoglycemia, diabetes, bankruptcies, divorce, mothers (parents) killing children, road rage, school shootings, cancer, Chronic Fatigue Syndrome, and Fibromyalgia since these serotonergic drugs have become so popular and I relate it directly to the effects of these drugs.

The death toll has continued to climb drastically since I wrote PROZAC: PANACEA OR PANDORA? Some of the cases you may be familiar with are:

1. Mr. and Mrs. Phil Hartman (Zoloft), Prozac was found in the van of Mark Barton, the Atlanta day trader, who recently killed his family and others in a shooting spree before taking his own life;
2. Neal Furrow, in LA Jewish school shooting was reported to have been court ordered to be on Prozac along with several other medications;
3. The Salt Lake Family History Library shooting;
4. School shootings in Littleton, Colorado (Luvox), Atlanta, Georgia, Springfield, Oregon (Prozac), and Caldwell, Idaho;
5. Another boy in Pocatello, ID in 1998 who in seizure activity from Zoloft had a stand off at the school;
6. 15 year old Chris Shanahan (Paxil) in Rigby, ID who out of the blue killed a woman;
7. The shooting at the lottery in Connecticut last spring by Matthew Beck (Luvox) that left five dead in a murder/suicide;
8. The New York City Subway bombing by Edward Leary (Prozac);
9. Nick Mansies (Paxil) in New Jersey who was convicted of killing a little boy who was selling cookies door to door;
10. In Orange County, CA Dana Sue Gray (Paxil) who co-workers described as a very caring nurse killed several elderly people;
11. Officer Stephen Christian (Prozac) one of the finest officers on the Dallas Police force, who ran into a police substation shooting at fellow officers and was killed;
12. 13 year old Chris Fetters (Prozac) in Iowa who killed her favorite aunt;
13. David Rothman (Prozac) killed two co-workers and himself at the Dept. of Agriculture in Ingelwood, CA;
14. Williams Evans (Zoloft) shot one co-worker at the Ohio Bureau of Employment Services before shooting himself in Columbus, OH;
15. Winatchee, WA where 43 people were wrongfully imprisoned in a false accusation of sexual abuse “witch hunt” fury started by a child under the influence of Prozac and Paxil;
16. Christopher Vasquez (Zoloft) killed Michael Morrow in Central Park;
17. Megan Hogg (Prozac) duct taped the mouths and noses of her three little girls and took a handful of pills; Vera Espinoza (Prozac) in Randolph, VT shot her small son and daughter before shooting herself;
18. An elderly man (Prozac) in Layton, UT axed his wife and daughter to death;
19. Margaret Kastanis (Prozac) used a knife and hammer to kill her three children before stabbing herself to death;
20. An elderly man (Paxil) in Dallas, TX strangled his wife before shooting himself twice in the chest;
21. Larramie Huntzinger (Zoloft) blacked out and ran his car into three young girls killing two in Salt Lake City, UT;
22. Mary Hinkelman (Prozac), a nurse in Baroda, MI shot her two small daughters and her sister before shooting herself;
23. Lisa Fox (Prozac) shot her small son and her dog before shooting herself in Brighton, MI;
24. Debi Louselle (Zoloft) shot daughter and then herself in Salt Lake City, UT;
25. A father in Wyoming shot his wife, daughter and baby grand-daughter then himself after only days on Paxil;
26. A mother (Prozac) in Pleasant Grove, UT killed her 17 year old son with a sledge hammer while he slept before she attempted suicide by drinking Drano;
27. Larry Butz, a superintendent of schools in Ames, IA shot his wife, son and daughter before shooting himself – many cases pending in court are not mentioned.

This is only a handful of MANY, MANY more cases – there would not be room for anything else if I continued listing the cases.

A few additional famous victims: Princess Di (Prozac) and Dodi Fayed -via their driver Henri Paul (Prozac), Monica Lewinsky (Prozac, Zoloft, Effexor, Serzone and Phen-Fen), Chris Farley (Prozac), Pres. Clinton’s ex-partner Jim Mc Dougal (Prozac), Abby Hoffman (Prozac), Del Shannon (Prozac), Danielle Steele’s son (Prozac), INXS singer Michael Hutchence (Prozac), Sarah – Dutchess of York (Phen-Fen)

The latest figures show Prozac has about 44,000 adverse reports filed with the FDA. Out of those reports there are about 2,500 deaths with the large majority of them linked to suicide or violence.

The suicide statistics relating to women are shocking. According to the CDC there are about 30,000 suicides yearly in the United States. Out of those about 6,000 are women – a ratio of about 4.3 to 1, male to female. About twice as many women as men are treated for depression demonstrating that generally men are more than 8 times as lethal in their suicidal gestures as women. Women were known to use less lethal means until the SSRI antidepressants hit the market. But on Prozac and Paxil, women committed 40% of the suicides – many were strikingly violent and clearly leaving no
means for rescue. (Remember that because Prozac was the first of this group of drugs its track record gives us a vision of what is to come with other serotonergic antidepressants, especially when they are so powerful in the reuptake of serotonin.)

TIME LINE OF CRITICAL INFORMATION DISCOVERED SINCE THE BOOK:

*NOTE: Any documents beginning with PZ are Lilly documents on Prozac which have been ferreted out by attorneys and are now being used in lawsuits against the drug company. (Christian vs. Eli Lilly, by Vickery & Waldner, Houston, TX)

* Mid 1950’s: Dr. Felix Sulman began his research on those who suffer from high serotonin levels because of an inability to metabolize serotonin. He found that serotonin is a stress neuro-hormone leading even rabbits, the most docile of creatures, to be aggressive. He coined the term “serotonin irritation syndrome.” He found that those who were unable to break down serotonin would have the levels increase. They were in effect being poisoned by the serotonin produced by their own bodies, the irritation victims suffered from migraines, hot flashes, irritability, sleeplessness, pains around the heart, difficulty in breathing, a worsening of bronchial complaints, irrational tension and anxiety. . . horrifying nightmares. It also caused his volunteers to sleep badly – that is, always on the edge of consciousness so that they were not properly rested – and to wake after only a few hours of sleep.” (sleep apnea) He also found it caused pregnant women to abort.
* October, 1977: Slater, et.al., Inhibition of REM Sleep by Fluoxetine, a Specific Inhibitor of Serotonin Uptake, October 1977, at p. 385 – Prozac was found to affect sleep habits, specifically to suppress deep sleep, which the scientists call REM (rapid eye movement) sleep in cats. By the fourth day of drug treatment the cats receiving the larger doses, which had been friendly for years, began to growl and hiss. After cessation of the drug treatment, the cats returned to their usual friendly behavior in a week or two; those on the higher doses recovering more slowly. – – 1977: [PZ 1298 1999] “A total of six dogs from the high dose group were removed from treatment … due to severe occurrences of either aggressive behavior, ataxia, or anorexia.”]
* July 31, 1978: [PZ1061 1025-28, July 31, 1978] Human subjects began to be used by Lilly in controlled clinical trials. The first group of patients showed no improvement in their depression, but there were a “large number of reports of adverse reactions.” The first human to receive Prozac experienced “dystonia resembling an extrapyramidal reaction” – an uncontrollable, Parkinson-like shaking or trembling.
* July 23, 1979 [PZ 1297 969] The clinical studies in depression showed that “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. In future studies the use of benzodiazepines to control the agitation will be permitted.”
* August 3, 1979: The clinical trials excluded patients who had serious suicidal risk. [E.g. control #001519, IND Protocol No. 14, August 3, 1979; PZ1135 695, July 2, 1986 memorandum of Dr. Wernicke].
* December 17, 1984: [PZ 65 449, report of Lilly to FDA] Lilly reported to the FDA that benzodiazepines and other sedatives were given with Prozac throughout the clinical trials. This was to help offset the stimulant effect of the drug. In a memorandum of Lilly scientist Charles Beasley [PZ 541 2007-08] issues of “agitation vs. sedation” and concomitant sedative medications like benzodiazepines (to control the agitation) are discussed. Concerns are that agitation in a suicidal patient can induce suicide.
* March 3, 1986 Lilly controlled the flow of information to the FDA and decided that suicide data on Prozac should not be evaluated, “in the safety-update for the FDA the number of suicides and suicide attempts will not be especially evaluated.” [PZ 879 1966, March 3, 1986 telex]
* September 12, 1986: German BGA very concerned with the risk of suicide and ultimately approved Prozac on the condition that physicians be warned of the risk of suicide and told to consider using sedatives and closely monitor patients. [PZ 878 1383, report of Lilly consultant Pohlmeier; PZ 2467 299, September 12, 1986] Lilly actually warned physicians in Germany and other countries that this measure “can be necessary” to minimize the risk of suicide, [PZ 1341 402, December 6, 1989 German warning; PZ 2469 490]
* February 7, 1990: In response to the Harvard study, Teicher, et al., Lilly’s top scientist, Leigh Thompson, told his fellow executives that “Lilly can go down the tubes if we lose Prozac”. [PZ 1941 827, February 7, 1990]. In the ensuing months Dr. Thompson spoke frequently with his principal FDA regulator about the issue, once at 6:15 in the morning. [PZ 391 1959, July 18, 1990]. Lilly later described the man as “our defender”. [PZ1941 2256, September 12, 1990]
* May 29, 1990, Lilly added “suicidal ideation” in the section dealing with post-marketing reports. [PZ883 562, July 26, 1990 memorandum]
* September 14, 1990: Contrary to the advice of his staff, Dr. Thompson told the Eli Lilly Board of Directors that suicide and hostile acts were probably, caused by the patients’ underlying disorders rather than Prozac. [PZ542 2101, September 14, 1990; PZ4002 889, Board Minutes]. The staff was concerned because they knew that this issue was never studied during the clinical trials.
* September 11, 1990: Note from Dr. Bruce Stadel, Chief of the Epidemiology Branch, attaching an analysis done by Dr. David Graham, Section Chief within the Epidemiology Branch, of Lilly’s July 17, 1990 submission to the FDA on the Prozac/suicidality/violence issue. The following factors were (a) brought to the attention of those in the higher echelons of the FDA, but (b) ignored, discounted or “trashed” by them: #1 Lilly’s analysis improperly excluded 76 out of 97 suicides; as Dr. Stadel expressed it, “[i]t is inappropriate in a safety analysis to exclude such a large proportion of case”; #2 Lilly admitted that its clinical trials “were not designed for the prospective evaluation of suicidality” and that “[i]n these trials, patients with current suicidal ideation were excluded”; #3 Lilly admitted that the HAMD-3 rating scale it used to assess suicidality in clinical trials was inadequate; and that Lilly’s statements about violence only demonstrated “how great under-reporting is” and that “[t]he actual data showed a higher percentage of treatment-emergent suicidality among fluoxetine (2.9% than tricyclic (0.8%) patients . . . [which percentage] was similar to that reported by Teicher.”
* July 1, 1992: A study lead by Dr. Lorne Brandes of the Manatoba Institute of Cell Biology in Winnipeg, Canada was published in CANCER RESEARCH linking the two most popular anti-depressants, Elavil and Prozac to cancer.
* 1994: A study headed by Howard Markell published in The Journal of Pediatrics showed LSD flashbacks and LSD reactions induced by Prozac.
* June 9, 1994: The New York Review of Books article by Dr. Sherwin Nuland slams Peter Kramer for pushing Prozac in his book Listening to Prozac. He pointed out that all docs are taught in med school this little poem about serotonin: “This man was addicted to moanin’, confusion, edema, and groanin’, intestinal rushes, great tricolored blushes, and died from too much serotonin.” He listed constriction of lungs and intestines, diarrhea, wheezing, flushing, mental confusion, tightening of bronchioles, and lessening conscious control over behavior from increases in serotonin. “Moreover, . . . it is still too early to arrive at a reliable estimate of possible dangers that may appear in the long term,” and 15% dropped out of the clinical trials on Prozac because of adverse reactions. He also discussed the similarity of serotonin to the psychedelics like LSD and PCP.
* November, 1994: Krystal JH, Webb E, Cooney N, et al., “Specificity of Ethanol-like Effects Elicited in Serotonergic and Noradrenergic Mechanisms,” ARCHIVES OF GENERAL PSYCHIATRY, Vol. 51, Issue 11, pgs 898-911, 1994 demonstrated that an increase in brain levels of either of two neurotransmitters, serotonin or noradrenalin, produces:
#1 a craving for alcohol,
#2 anger,
#3 anxiety.
They found this to be especially true for those who have a history of alcoholism. An increase serotonin in turn increases noradrenalin. Numerous reports have been made by reformed alcoholics who are being “driven” to alcohol again after being prescribed a serotonergic drug. And many other patients who had no previous history of alcoholism have continued to report an “overwhelming compulsion” to drink while using these drugs.

A few personal accounts:

#1 A young woman, a recovering alcoholic, reported that during the eight month period she had been using Prozac she found it necessary to attend AA meetings every day in order to fight off the strong compulsions to begin drinking again.
#2 In the Southeastern United States a middle aged psychologist, also a recovering alcoholic, after being prescribed Prozac, found herself needing to attend AA meetings morning, noon, and night to keep from destroying the sobriety she had achieved.
#3 A young father, who was Mormon and had never before in his life used alcohol, found himself drinking Ever Clear and exhibiting bizarre as well as violent behavior, after being prescribed Prozac and Ritalin.
#4 A young mother who had never used alcohol before began drinking large amounts within weeks of being prescribed Prozac and quickly found herself committed to a mental institution due to the psychotic behavior that resulted. Added to her Prozac prescription were anti-psychotic meds and electric shock treatments. She then began to experience seizures and was started on anti-seizure meds.
#5 A concerned neighbor reported her friend was drinking straight Vodka on a regular basis after being prescribed Zoloft. #6 A daughter reported her father, sober for 15 years, began drinking again on Prozac.

* December, 1994: Not guilty verdict on Wesbecker wrongful death suit against Lilly’s Prozac.
* Treatment emergent suicidality with Prozac has been demonstrated to be two to three times higher than any other anti-depressant. (Jick, et al., Antidepressants and Suicide)
* May, 1995: Judge John Potter who presided over the Wesbecker case filed documents to demand that Lilly be forced to disclose the secret deal they made with the plaintiffs to withhold very damaging evidence in exchange for settlement. In his pleading to the court Potter stated, “Lilly sought to buy not just the verdict, but the court’s judgment as well.” Potter accused Lilly of “giving the verdict the widest possible publicity” accompanied by the claim that Lilly had “proven in a court of law that Prozac was safe.” Furious with Lilly’s attempt to turn his courtroom into an advertising agency for Prozac, he claims his motion reflects “the court’s duty to protect the integrity of the judicial system.” He believes, as do prominent legal ethicists, that a full and open disclosure of the terms of the settlement is a necessary public safety issue.
* July, 1997: Mayo Clinic found that the increased serotonin, which produces blood clotting, was causing a gummy glossy substance to build up on heart valves. Dr. Heidi Connolly with the Divisions of Cardiovascular Diseases and Internal Medicine, who headed the study stated, “We do know that fenfluramine and phentermine [Fen-Phen] alter the way the brain chemical serotonin is metabolized, and serotonin that circulates in the blood can cause valve injury.” Fenfluramine produces a rapid release of serotonin, inhibits serotonin reuptake, and may also have receptor agonist activity. The study’s revelations should send a loud and very clear warning throughout the medical community concerning all serotonergic medications.
* August 25, 1997: Letter to Ann Blake-Tracy, “I caught the last part of your presentation on Radio Station KEX, Portland, while flipping through the dial last night. I was flabbergasted to hear you speak of the horrible potential side effects from Prozac, which I have been taking for approximately four years, particularly since I have been diagnosed recently with cardiomyalgia, severe artery disease, congestive heart failure and also Fibromyalgia. (I was a very “well” person prior to taking the Prozac and am now exhausted all the time, with horrible aching joints and considerable pain and a massive heart problem.) The adverse cardiovascular effects from Prozac, the one drug in this class of drugs out long enough to have somewhat of track record, are listed in the drug information sheet put out by the manufacturer. The “frequent” effects listed are hemorrhage and hypertension. The “infrequent” effects include very serious adverse effects: congestive heart failure, myocardial infarct, tachycardia, angina pectoris, arrhythmia, hypotension, migraine syncope and vascular headache.
* September, 1997: Redux and Phen-Fen were pulled from the market.
* October 20, 1997: Dr. Candace Pert, Research Professor at Georgetown University Medical Center, past head of the brain chemistry department at the National Institute of Health, and author of the new book, MOLECULES OF EMOTION, sounded an alarm in TIME, October 20. She stated, “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. Prozac and other antidepressant serotonin-receptor-active compounds may also cause cardiovascular problems in some susceptible people after long-term use, which has become common practice despite the lack of safety studies.”
As we are being led to believe these drugs produce effects only in the brain, Dr. Pert accuses the medical profession of oversimplifying the action of these drugs and adds that “the public is being misinformed about the precision of these selective serotonin-uptake inhibitors.” It is critical that both physicians and patients be made aware of these adverse physical reactions. She points out that the medical profession not only oversimplifies the action of these drugs in the brain, but “ignores the body as if it exists merely to carry the head around!” And that, “these molecules of emotion regulate every aspect of our physiology.” The body plays a very significant role in how we feel and act the way we do. This fact can no longer be ignored. Serotonin and serotonin receptors exist throughout the body, as well as the brain, and every aspect of the body’s physiology is affected by these serotonergic medications. In fact approximately 90% of the body’s serotonin is produced in the intestinal tract. According to Dr. Michael Gershon of New York’s Columbia Presbyterian, this is the reason why Prozac produces so many gastrointestinal side effects.
* March, 1998: Two new studies published. One that shows Prozac so strongly inhibits one particular serotonin receptor that this produces both obesity and seizures and the other discusses the blockage of muscle and neuronal nicotinic acetylcholine receptors indicating interactions between the serotonergic and cholinergic systems in the central nervous system.
* April, 1998: Our next generation of guinea pigs – one month before a 15 year old on Prozac, Kip Kinkel, in Springfield OR killed his parents and two classmates the American Psychiatric Association and the American Academy of Pediatric Psychiatrists asked the FDA to consider the serotonergic antidepressants for use in children as young as two and drugs for anxiety, aggression and manic depression in babies only one month old! The use of Prozac among young children ages 6 – 12 has increased an alarming 400% from 1995 (51.000 new prescriptions) to 1996 (203,000 new prescriptions).
* June, 1999: CLINICAL PSYCHIATRY NEWS reported that Dr. Malcolm Bowers a psychiatrist at Yale has found that physicians are not paying enough attention to patient factors that could make initiation of SSRIs dangerous. He found that “SSRI-induced psychosis has accounted for 8% of all general hospital psychiatric admissions over a recent 14-month period.” And “What is surprising is that this particular group of side effects is really underplayed.” (The 8% figure represents over 150,000 SSRI induced psychotic breaks per year!!!!!!!)

WARNING: Children so often get coughs and colds, yet using a cough or cold medication with dextromethorphan could cause the serotonin syndrome, a very serious and potentially fatal adverse reaction and/or produce PCP reactions.

Serotonin syndrome remains an often misdiagnosed or unrecognized fatal reaction due to the medical profession being so uninformed about this drug-induced disorder.

Developing brains are far more vulnerable than adult brains and brain damage generally becomes more apparent after the brain is fully developed, rather than immediately. Increases in cortisol produce brain damage while medical research shows that one single 30mg dose of Prozac DOUBLES the level of cortisol. This drastic increase in cortisol causes a multitude of serious physical reactions including impairment of linear growth, as well as impairing the development and regeneration of the liver, kidneys, muscles, etc. In light of so many unspeakable tragedies, I have grown weary of all the silly philosophical discussions we have heard since Kramer’s LISTENING TO PROZAC came out. Patients are dying or having their health destroyed mentally as well as physically (when do we begin to discuss the very serious physical side effects associated with high levels of serotonin?). These patients and their families are frantically searching for answers while this research sits right under our noses and could easily be made available to them. The widespread use of Prozac and its clones is not a statement of either their safety or their effectiveness. It is a statement about the effectiveness of an infinite marketing budget and incredible advertising campaign! These drugs have very serious physical side effects, as well as dangerous psychiatric side effects.

To prevent further tragedy this medical research must be acknowledged and addressed in headline news without delay rather than remain buried in seldom read medical research documents as has been the case in the past with other mind- altering medications, once thought to be safe, which were subsequently prohibited by law, i.e. LSD, PCP, cocaine, etc.

PRAISE FOR PROZAC: PANACEA OR PANDORA?

“I started having bad reactions . . . Oct ’96 I found Prozac to be causing joint and muscle pain itself . . . signs of Cushing’s Syndrome. . . I was very pro-Prozac until last October and wouldn’t have listened to anything said against it until I got problems (thought it was saving my life, while all the time it was insidiously and interested but quite skeptical. However, since reading it and having suffered so many problems with Prozac, I have come to the conclusion that the book is brilliant, and a life-line as far as I am concerned. I tried to fault the research and reasoning, but could not and still can’t. I would like to extend my thanks to you for your heroic stance on this enormously important issue. I have tremendous respect and admiration for your hard work, determination and courage in pursuing this subject so vigorously, against so much powerful opposition for the benefit of people like me. Your integrity puts many, if not most doctors and psychiatrists to shame. It is reassuring to find that there are a few people who are prepared to fight for the truth for the benefit of mankind.” Oct. 1998 note from a British nurse

“PROZAC: PANACEA OR PANDORA? is an incredible compilation of medical data that will lay the groundwork to educate other professionals and the general public about the new SSRI antidepressants – Prozac, Zoloft, Paxil, Luvox, Effexor and Serzone.” (Jeff Wise, psychologist, Salt Lake County Drug and Alcohol Abuse )

“In 15 years of reading books on drugs I have never read a book with more information or so well documented as PROZAC: PANACEA OR PANDORA?” (Dr. Kevin Millet, Bountiful, UT)

“As I lecture to physicians nationwide on the medical use of psychoactive drugs PROZAC: PANACEA OR PANDORA? always accompanies me in my brief case.” (Dr. Bruce Woolley, neuropsychopharmacologist, Brigham Young University)

“I found PROZAC: PANACEA OR PANDORA? fascinating reading and the most complete analysis of the various factors pertaining to the Prozac controversy.” (Attorney Donald Sokol, Susanville, CA)

“PROZAC: PANACEA OR PANDORA? literally saved my life, and if I’d known about it a year earlier, could have saved me untold grief and agony as well. It is the only collated, comprehensive source I know of for this information , . . .. this book described everything that had happened to me in great detail, gave scientific reasons why it happened, backed it all up with solid research, included testimonials from hundreds of others in the same situation, it immaculately details, explains, and refers one to the latest research on a whole hornet’s nest of ‘atypical’ side-and/or after-effects from the use of these antidepressants. It also contains information on how to reduce the severity of problems encountered while starting on or going off these meds.” (Nick Jameson, Prozac patient)

“Magnificent! This text is a monument to Ann Tracy’s tenacity and love for her fellow human beings.” (Dr. Paul Kennedy, N.J.)

“PROZAC: PANACEA OR PANDORA? has not left one question about these drugs unanswered! Ann Tracy has covered them all.” (Margaret McCaffery, N.Y. who lost her daughter, a neurosurgeon, in a Prozac suicide)

“The work Ann Blake-Tracy is doing is very important and she is truly a heroine.” (Dr. Candace Pert, Washington, DC, one of the two developers of the serotonin binding process which made possible the development of the serotonergic drugs. Dr. Pert has boldly stated, speaking of these serotonergic medications, “I am alarmed at the monsters I created!”)

WARNING: In sharing this information about adverse reactions to antidepressants I always recommend that you also give reference to my CD on safe withdrawal, Help! I Can’t Get Off My Antidepressant!, so that we do not have more people dropping off these drugs too quickly – a move which I have warned from the beginning can be even more dangerous than staying on the drugs!

The FDA also now warns that any abrupt change in dose of an antidepressant can produce suicide, hostility or psychosis. And these reactions can either come on very rapidly or even be delayed for months depending upon the adverse effects upon sleep patterns when the withdrawal is rapid! You can find the CD on safe and effective withdrawal helps here: http://store.drugawareness.org/

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6/1/1999 • Fluoxetine treatment of depression. Clinical effects, drug concentrations and monoamine metabolites and N-terminally extended substance P in cerebrospinal fluid.

6/1/1999 • Fluoxetine treatment of depression. Clinical effects, drug concentrations and monoamine metabolites and N-terminally extended substance P in cerebrospinal fluid.

Martensson B, Nyberg S, Toresson G, Brodin E, Bertilsson L
Department of Psychiatry, Karolinska Hospital, Stockholm, Sweden.

Acta Psychiatr Scand 1989 Jun; 79(6); 586-96

During treatment the 5-HIAA concentration decreased by 46%.

Fluoxetine treatment of depression. Clinical effects, drug concentrations and monoamine metabolites and N-terminally extended substance P in cerebrospinal fluid.

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=2475012&dopt=Abstract

Martensson B, Nyberg S, Toresson G, Brodin E, Bertilsson L
Department of Psychiatry, Karolinska Hospital, Stockholm, Sweden.

Acta Psychiatr Scand 1989 Jun; 79(6); 586-96

During treatment the 5-HIAA concentration decreased by 46%.

In an open study of depressed inpatients, the effects of the selective serotonin uptake blocker fluoxetine on 5-hydroxyindoleacetic acid (5-HIAA), homovanillic acid (HVA), 4-hydroxy-3-methoxyphenyl glycol (HMPG) and N-terminally extended substance P (SP) in cerebrospinal fluid (CSF) were measured. Thirteen unmedicated patients who met the DSM-III criteria for major depressive episode were included, and 9 completed the study. During treatment the 5-HIAA concentration decreased by 46%. The HVA and HMPG concentrations also decreased significantly, but to a lesser degree. The mean level of N-terminally extended SP was unaffected by fluoxetine treatment, but the pretreatment level correlated significantly with the pretreatment level of HMPG. The pretreatment level of HVA was the only biochemically variable that appeared to predict therapeutic outcome. The plasma concentrations of both fluoxetine and its metabolite norfluoxetine increased significantly between 3 and 6 weeks. Plasma and CSF levels of both the parent drug and its active metabolite were correlated.
PMID: 2475012, UI: 89348863

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