Author Topic: FDA warning on SSRIs  (Read 56103 times)

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Offline Anonymous

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FDA warning on SSRIs
« Reply #135 on: September 08, 2004, 01:02:00 PM »
unfortunately this issue of prozac and anger with the child that shot his dad is not a prozac issue.  the dad was shot by the mom through the manipulation of the child.  she wanted the father dead.  the child was not abused by the father.  he was emotionally abused by the mother.  she abused him over a long period of time and put him on prozac as a defense for the senseless crime she had him pull off.  it is a shame to waste all the discussion about prozac in this case because  so much is yet to come out that the public is not aware of.  wait and see and the truth will come out.  the mother is not a fit mother for pitting her own children against the dad for so long.  it is sad story, but dont think that the boys were abused by the dad. it simply is not true.  two police depts and CPS investigated and didnt even press charges.  they found the boys to say that the mom had told them to say it.  what awful things to put your children through.  dont waste your time thinking the prozac provoked this child to kill.  it was careful, thought out, calculated manipulation on the part of the mother.  she knows what she has done - it is just a matter of time before everyone else will too.
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Offline Anonymous

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« Reply #136 on: September 08, 2004, 05:05:00 PM »
How is it that you have the 'inside' scoop? Family, friend, CPS worker...dad....
Are there any newspaper articles to support your comments? Particularly:

"it simply is not true. two police depts and CPS investigated and didnt even press charges. they found the boys to say that the mom had told them to say it."

So, dad was investigated for abuse, but no one thought it might be a good idea to check mom out, if indeed the boys reported that she had told them to say they were abused? The dad never tried to have that established and/or seek custody?
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Offline Anonymous

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« Reply #137 on: September 09, 2004, 10:49:00 AM »
http://energycommerce.house.gov/108/Hea ... earing.htm

Publication and Disclosure Issues in Anti-Depressant Pediatric Clinical Trials
Subcommittee on Oversight and Investigations
September 9, 2004
2123 Rayburn House Office Building
11:00 AM

Hearing Webcast: Pending

The hearing will begin at approximately 11:00 AM. The link to the broadcast will become active 10 minutes prior to the start of the hearing. Refresh your browser for the latest information.

Committee web casts require the free Real Player.
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Offline Deborah

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« Reply #138 on: September 10, 2004, 01:07:00 PM »
DRUG Firms Blasted for Hiding Antidepressant Data
NPR (audio) - USA
http://npr.streamsage.com/google/progra ... id=3910628

In Capitol Hill hearings, lawmakers criticize drug manufacturers for failing to fully disclose data on the use of antidepressants by children ...

See all stories on this topic:
http://tinyurl.com/6nqp4
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Offline Deborah

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« Reply #139 on: September 16, 2004, 11:15:00 AM »
Don't miss this interview if your child is taking or you are considering antidepressants for your child. A bluntly honest and articulate parent- witness at the FDA hearings- speaks about the fraud that resulted in her daughter's death.
http://www.msnbc.msn.com/id/5989348/

From the text at that page:
Dr. Matthew Rudorfer, a mood disorder specialist at the National Institute of Mental Health, voted against the black box warning. The 2 percent to 3 percent increased risk of suicidal thoughts that alarmed the panel was overshadowed by the 15 percent risk of suicides by children with untreated depression. "I fear the black box would impede access to treatment," Rudorfer said.

And from another article:
http://www.nytimes.com/2004/09/14/healt ... ss.html?th

In 2002, nearly 11 million children and teenagers were prescribed antidepressants. The risk of suicide among patients given the pills is very small.  If 100 children and teenagers are given antidepressants, 2 or 3 will become suicidal who otherwise would not have had they been given placebos, agency officials said.  None of the children in the trials committed suicide, but some thought about or attempted suicide, researchers found.
***

First, no one committed suicide in trials? What about Traci Johnson? Any others? http://www.google.com/search?hl=en&ie=U ... 2B+suicide)

Question- Is it two or three? Or 2.5, or 2.3, or 2.9?
"15% risk of suicides by children with untreated depression"? What exactly is Rudorfer saying?  15% of untreated kids are at risk; OR untreated kids are 15% more likely to commit suicide? I assume the former.  How was this determined? How do they know how many children have 'untreated depression' and what the percentage is who are at risk of suicide?

So, if 15% of untreated kids are at risk, how many kids are depressed? Good luck finding that information. The percentages I found ranged from 2-10%. Who's counting? Can't they get more accurate?
This one says 1 in 12 adolescence and 5% of  9- 17 yr olds.
http://www.safeyouth.org/scripts/teens/depression.asp

Given there were 60,000,000 kids between the ages of 5-18 in 2000;  2-10% of 60mil would be 1,200,000 - 6,000,000 who are presumed to be depressed. Those are quiet large numbers and a significant gap. Oh well, so it goes in the world of make believe.

If 15%, as Rudorfer claims, of those untreated kids are at risk, that would be 180,000- 900,000 kids who are at risk of suicide from 'untreated depression'.

Interestingly enough, according to the CDC, out of 60 million children between the ages of 5- 18 in the US (in 2000), there were 1493 suicides- .000025- or 25 suicides per million.  And how many of those were taking antidepressants at the time of their suicide?

This healthcare website states that 5,000 teens commit suicide each year. Where do they get their stats?
http://www.srhs.org/betterhealth3.asp?StoryID=296

An important consideration:
As the above article stated that 2 to 3% of teens on antidepressants think about or attempt suicide.  Did that grab your attention? No- sounds like a pretty small, and insignificant number; and according to Rudorfer, pales in comparison to the 15% at risk who are 'untreated'.  But, with 11,000,000 kids on antidepressants that means 220,000 to 330,000 of them will consider or attempt suicide.

Do the benefits really outweigh the risks? Is the window of loss acceptable?

Are there really 180- 900,000 kids at risk of suicide from untreated depression? I'm more inclined to imagine that to be the number of kids the drug companies project will be placed on antidepressants with the Bush 'mental health' screening initiative. Another excellently executed BushCo business plan.

Does it really make sense to subject 220-330,000 kids to thoughts of or attempts at suicide when the current stats show that only 25 per million 5-18 year olds actually commit suicide?

Particularly when, Dr. Andrew D. Mosholder, a senior epidemiologist at the FDA who assesses the safety of medicines, found last year that 22 studies showed that children given antidepressants were nearly twice as likely to become suicidal as those given placebos.
http://www.nytimes.com/2004/08/20/scien ... press.html

And, studies such as this have shown that children who took sugar pills (placebo) children showed strong improvement and those who took the real drugs didn't do significantly better. Two small studies found no advantage for the antidepressants over the placebo.
http://www.canada.com/edmonton/edmonton ... 35936948ed
***

Unfortunately, The ANTI forced "mental health screening" Amendment offered by Congressman Ron Paul [Texas] failed by a vote of 95-315.

Sign the petition to oppose mandatory mental health screening at:
http://www.prweb.com/releases/2004/9/prweb156052.php

TeenScreen has the state goal to "Screen 40,000+ teens and refer more than 10,000 for treatment:
http://www.teenscreen.org

Other news
http://www.alertnet.org/thenews/newsdesk/WBT001672.htm
Excerpt:
A U.S. advisory panel urged regulators on Tuesday to require a "black box" warning on antidepressant labels about the increased risk of suicidal behavior in youth who take the drugs.
A black box is the strongest type of warning the Food and Drug Administration uses for prescription drugs. The FDA will consider the panel's recommendation, which passed 15-8 in favor of the boxes
***

http://www.washingtonpost.com/wp-dyn/ar ... 4Sep9.html
Excerpt:
The Food and Drug Administration has repeatedly urged antidepressant manufacturers not to disclose to physicians and the public that some clinical trials of the medications in children found the drugs were no better than sugar pills, according to documents and testimony released at a congressional hearing yesterday.
Regulators suppressed the negative information on the grounds that it might scare families and physicians away from the drugs, according to testimony by drug company executives.
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Offline Deborah

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« Reply #140 on: September 16, 2004, 12:32:00 PM »
If you miss the show, it can be found in the archives at the link below.

TONIGHT, September 16, 2004 @ 5pm Pacific Standard Time:  DANGERS OF PSYCHIATRIC DRUGS - PART 3:
   
Topic:    Post FDA / Congressional Hearings on Suicide Induced SSRI-s in Children and Adolescents.

http://www.worldtalkradio.com/archive.asp?aid=2260

Joining Annie Armen on AAL tonight:

Legal Expert Guest: Karen Barth Menzies, Esq. - Reputable partner in the national law firm of Baum Hedlund; lead attorney on dozens of antidepressant (SSRI) suicide and violence cases involving Paxil and Zoloft.

Expert Guest: Karen Effrem, M.D., - Pediatrician, researcher, conference speaker, and leading opponent of mandatory screening who serves on the boards of three national organizations: EdWatch, ICSPP, and the National Physicians Center.  

Special Guest: Patricia Weathers ? President & Founder of Ablechild.org, Parents for Label and Drug Free Education who fights for parental and children?s rights!

Expert Guest, Author: Fred Baughman, Jr., M.D., has been an adult and child neurologist in private practice for 35 years. Dr. Baughman has testified for victimized parents and children in ADHD/Ritalin legal cases, and writes powerful,
resourceful articles in exposing the fraud of ADD / ADHD.

This show is sponsored in part by ISAC Corporation.  
Check out ISAC's New Company Distinguished Guest Page on Annie Armen Live by visiting http://www.worldtalkradio.com/guests.asp?sid=97,
and please show your support by visiting http://www.isaccorp.org.
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Offline Deborah

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« Reply #141 on: September 22, 2004, 07:46:00 PM »
http://www.click2houston.com/news/3750858/detail.html
 
Slain Doctor's Parents Sue Drug Maker, Ex-Wife
Lohstroh's Parents, Friends Say Father Did Not Want Son, 10, On Prozac
POSTED: 8:04 am CDT September 22, 2004
UPDATED: 5:10 pm CDT September 22, 2004

HOUSTON -- The parents of a murdered doctor filed a wrongful death lawsuit Wednesday afternoon against their former daughter-in-law and a pharmaceutical company, Local 2 reported.  

Police said Rick Lohstroh's 10-year-old son fatally shot him outside his ex-wife's Katy home on Aug. 27 as he picked him and his 8-year-old brother up as part of a joint custody agreement. Lohstroh's parents -- Richard and Joanne Greene -- filed a lawsuit against Deborah Geisler, the boy's mother, and the maker of Prozac, Ely Lilly and Co. "Today we are filing suit on behalf of Dick and Joanne Greene for the tragic death of their son, Rick," said David Matthews, an attorney. Lohstroh's parents and friends said Rick Lohstroh was upset with Geisler for putting their son on Prozac, which happened one month before his death. "In the week prior to the shooting, the boy's doctor increased his dosage of Prozac. This is really important for two reasons," Matthews said.

Matthews said studies show a change in dosage can lead to violence and the drug's adverse effects are more severe in children. The 12-page lawsuit argues that Ely Lilly and Co. is to blame for Lohstroh's murder.

The Harris County Sheriff's Department said the 10-year-old retrieved a gun, climbed in the back seat and began shooting "through the back of the driver's seat, striking his father." Deputies said the boy got out of the vehicle and continued firing before going inside the home, where his mother took the gun from him. Investigators said it is still a mystery as to why the boy would kill his father, a 41-year-old physician at the University of Texas Medical Branch in Galveston.

During the couple's divorce trial, Geisler accused Lohstroh of sexually abusing their two sons. Two separate police agencies investigated the claims, but neither filed charges. People close to Lohstroh and his children say Geisler used a form of brainwashing, known as Parental Alienation Syndrome, during the couple's contentious breakup that they believe possibly led to the father's death.
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Offline Deborah

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« Reply #142 on: September 24, 2004, 01:14:00 PM »
This Houston news clip states that the mom was named in the lawsuit (1 page vs 12 for Ely Lilly) not for manipulating the boy, but for not keeping her gun more secured,and as an RN, for not 'monitoring' her child's medication more closely.

http://www.click2houston.com/news/3750858/detail.html
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Offline Deborah

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« Reply #143 on: September 25, 2004, 10:57:00 PM »
http://www.firstcoastnews.com/health/ne ... ryid=24746

WASHINGTON (AP) -- A government epidemiologist said Thursday that his bosses asked him to soften his recommendation that antidepressant use by children be discouraged because of increased suicidal behavior among young people who took the drugs.
During discussions with his managers at the Food and Drug Administration in March, "alternative conclusions were offered to me, which I declined to incorporate into my written document," said Andrew Mosholder, who works in the FDA's Division of Drug Risk Evaluation.
Instead of discouraging the use of all but one antidepressant, Prozac, for children, he was told to suggest that children use such  medication "with caution," Mosholder told a House subcommittee.
Mosholder said his reviews showed that Prozac, the only drug approved to treat depressed children, also posed the least risk for depressed children.
It's standard for superiors to review conclusions to ensure they're supported by the evidence, countered Dr. Paul Seligman, acting director of the agency's Office of Drug Safety, outside the hearing room.
"That was done in this case. There was never any pressure to change what he wrote," Seligman said. He termed managers' comments as "suggested language" that Mosholder could adopt or ignore. "He chose not to use it."
As is normal, the managers voiced their dissenting views in a cover letter, Seligman said.
An FDA advisory committee recommended last week that all antidepressants come with the agency's strongest warning, in a black box on the label, that the drugs increase suicidal behavior in children and teenagers. Among other suggestions, it said parents should be given detailed guidance on how to balance that risk with the benefit of treating depression.
The FDA often follows its advisers' recommendations but is not bound by them.
On Thursday, some members of the House subcommittee accused the FDA of a pattern of deception.
"No agency charged with protecting the public health should have behaved with such indifference to the public safety as is evidenced in this case," said Rep. Peter Deutsch, D-Fla.
Mosholder told the panel that by last December his work confirmed his preliminary analysis that found that children taking Paxil and seven other antidepressants suffered increased suicidal behavior more often than children taking sugar pills.
That finding was confirmed by an FDA senior reviewer who found that for every 100 children taking antidepressants in controlled clinical trials, an additional two to three experienced increased suicidal tendencies.
Mosholder said the FDA deferred action on his recommendations so it could confirm, through internal and external analyses, that the warning signs were legitimate.
At the same time, British regulators acted swiftly, strongly cautioning against prescribing antidepressants other than Prozac to children. That alarmed the investigative panel, which is looking into whether the agency squelched damaging information about the drugs.
Mosholder told the subcommittee that he was not allowed to present his findings at an FDA advisory meeting last February, and that he found himself the target of an internal affairs investigation seeking the source of a leak to the media about those findings.
Deutsch said the FDA attempted, without success, to force Mosholder to sign a document that eliminated all mention of the investigation. Contradicting Deutsch's statement, Mosholder testified he was not asked to sign the statement, but to simply present the edited document to the Senate. Acting on the advice of his attorney,
Mosholder used his own summary.
Rep. Joe Barton, R-Texas, chair of the investigative panel, said the agency's actions with Mosholder continued a pattern of deception that began as early as eight years ago. In 1996, Dr. James Knudsen, an FDA medical reviewer, linked Zoloft with increased suicidal thoughts and actions by suicidal children. In 1997, Mosholder raised concerns that Luvox heightened hostility among just depressed children, not adults taking it, Barton said.

"This hearing illustrates a larger problem at FDA, where too often drug companies trump parents, where medical evidence is suppressed and where expert opinion is silenced," added Bart Stupak, D-Mich.
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Offline Deborah

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« Reply #144 on: September 28, 2004, 11:44:00 PM »
http://www.motherjones.com/news/feature ... rders.html

This lengthy and indepth look at the industry will make it painfully obvious what's behind Bushs' initiative to screen the entire population for mental illness. These are but a few of the highlights:

  Disorders Made to Order

  Pharmaceutical companies have come up with a new strategy to market their drugs: First go out and find a new mental illness, then push the pills to cure it.
  By Brendan I. Koerner
  July/August 2002 Issue  

  Word of the hidden epidemic began spreading in the spring of 2001. Local newscasts around the country reported that as many as 10 million Americans suffered from an unrecognized disease. Viewers were urged to watch for the symptoms: restlessness, fatigue, irritability, muscle tension, nausea, diarrhea, and sweating, among others.  The disease was generalized anxiety disorder (GAD), a condition that, according to the reports, left sufferers paralyzed with irrational fears. Mental-health advocates called it "the forgotten illness." Print periodicals were awash in stories of young women plagued by worries over money and men. "Everything took 10 times more effort for me than it did for anyone else," one woman told the Chicago Tribune. "The thing about GAD is that worry can be a full-time job. So if you add that up with what I was doing, which was being a full-time achiever, I was exhausted, constantly exhausted."
   GlaxoSmithKline's modus operandi-marketing a disease rather than selling a drug-is typical of the post-Prozac era. "The strategy [companies] use-it's almost mechanized by now," says Dr. Loren Mosher, a San Diego psychiatrist and former official at the National Institute of Mental Health. Typically, a corporate-sponsored "disease awareness" campaign focuses on a mild psychiatric condition with a large pool of potential sufferers. Companies fund studies that prove the drug's efficacy in treating the affliction, a necessary step in obtaining FDA approval for a new use, or "indication." Prominent doctors are enlisted to publicly affirm the malady's ubiquity. Public-relations firms launch campaigns to promote the new disease, using dramatic statistics from corporate-sponsored studies. Finally, patient groups are recruited to serve as the "public face" for the condition, supplying quotes and compelling human stories for the media; many of the groups are heavily subsidized by drugmakers, and some operate directly out of the offices of drug companies' P.R. firms.
  The strategy has enabled the pharmaceutical industry to squeeze millions in additional revenue from the blockbuster drugs known as selective serotonin reuptake inhibitors (SSRIs), a family of pharmaceuticals that includes Paxil, Prozac, Zoloft, Celexa, and Luvox. Originally approved solely as antidepressants, the SSRIs are now prescribed for a wide array of heretofore obscure afflictions-GAD, social anxiety disorder, premenstrual dysphoric disorder. The proliferation of diagnoses has contributed to a dramatic rise in antidepressant sales, which increased eightfold between 1990 and 2000. Prozac alone has been used by more than 22 million Americans since it first came to market in 1988.
"You often hear: 'There are 10 million Americans with this, 3 million Americans with that,'" says Barbara Mintzes, an epidemiologist at the University of British Columbia's Centre for Health Services and Policy Research. "If you start adding up all those millions, eventually you'll be hard put to find some Americans who don't have such diagnoses."
  SmithKline's first forays into the anxiety market involved two fairly well-known illnesses-panic disorder and obsessive-compulsive disorder. Then, in 1998, the company applied for FDA approval to market Paxil for something called social phobia or "social anxiety disorder" (SAD), a debilitating form of shyness the DSM characterized as "extremely rare."
  With FDA approval for Paxil's new use virtually guaranteed, SmithKline turned to the task of promoting the disease itself. To "position social anxiety disorder as a severe condition," as the trade journal PR News put it, the company retained the New York-based public-relations firm Cohn & Wolfe. (Representatives of GlaxoSmithKline and Cohn & Wolfe did not return phone calls.)
  By early 1999 the firm had created a slogan, "Imagine Being Allergic to People," and wallpapered bus shelters nationwide with pictures of a dejected-looking man vacantly playing with a "If you are carrying out a disease-awareness campaign, legally the company doesn't have to list the product risks," notes Mintzes, the University of British Columbia researcher. Because the "Imagine Being Allergic to People" posters did not name a product, they didn't have to mention Paxil's side effects, which can include nausea, decreased appetite, decreased libido, and tremors.
 Journalists were given a press packet stating that SAD "affects up to 13.3 percent of the population," or 1 in 8 Americans, and is "the third most common psychiatric disorder in the United States, after depression and alcoholism."
Jack Gorman, the Columbia University professor who would later make the rounds on Paxil's behalf during the GAD media campaign. Gorman appeared on numerous television shows, including ABC's Good Morning America. "It is our hope that patients will now know that they are not alone, that their disease has a name, and it is treatable," he said in a Social Anxiety Disorder Coalition press release.
  Dr. Gorman was not a disinterested party in Paxil's promotion. He has served as a paid consultant to at least 13 pharmaceutical firms, including SmithKline Beecham, Eli Lilly, and Pfizer
  The lessons of "Imagine Being Allergic to People" were also not lost on Zoloft's manufacturer, Pfizer. In 1999, Pfizer gained FDA approval to market Zoloft as a treatment for post-traumatic stress disorder (PTSD). Until then, the condition had been associated almost exclusively with combat veterans and victims of violent crime; now, Pfizer set out to convince Americans that PTSD could, in fact, afflict almost anyone.
   In the months following the launch of Pfizer's campaign, media mentions of PTSD skyrocketed. Just weeks after the Alliance's founding in 2000, for example, the New York Times ran a story citing Pfizer-supplied statistics on childhood PTSD, according to which 1 in 6 minors who experience the "sudden death of a close friend or relative" will develop the disorder. Other stories highlighted studies promoted by the alliance according to which 1 in 13 Americans will suffer from PTSD at some point in their lives.
   Many of the statistics used to promote new disorders are taken from studies published in second-tier journals, which frequently depend on direct corporate support. One publication that has drawn fire is the Journal of Clinical Psychiatry, whose major funders include GlaxoSmithKline and Eli Lilly. In 1993, the journal published a study claiming that anxiety disorders cost the United States $46.6 billion per year, primarily due to lost productivity. That figure was repeated in countless press releases and made its way into articles in the Washington Post and USA Today.
  The study was produced by the Institute for Behavior and Health, a research firm headed by Dr. Robert DuPont, who served as President Ford's drug czar.
  Drug companies are understandably eager to help physicians identify conditions that can be treated with their products. One widely distributed diagnostic checklist, a 15-minute test that promises to screen for 17 different disorders using special software, was developed by GlaxoSmithKline. Pfizer has funded a test designed to help obstetricians and gynecologists identify women with mental-health problems. According to a 2000 study, sponsored by Pfizer and published in the American Journal of Obstetrics, a full 20 percent of all ob-gyn patients may need psychiatric treatment for anything from depression and anxiety to eating disorders.
 In 2000, the company gained FDA approval to market Prozac as a treatment for the condition; Eli Lilly promptly re-packaged Prozac as a pink-coated pill called Sarafem and launched a P.R. campaign warning that "millions of menstruating women" suffer from PMDD. "Does juggling work, family and personal commitments leave you feeling frazzled and stressed out?" the Sarafem Web site asks. "We have some tools to help."
 
  No such malady is yet listed in the DSM. But the quest for new uses for the SSRIs is continuing. At last year's annual convention of the American Psychiatric Association, researchers presented a major study on a new "hidden epidemic"-compulsive shop- ping. Jack Gorman, the Columbia psychiatrist who had earlier helped publicize anxiety disorders, made another appearance on Good Morning America to discuss the new condition, which host Charles Gibson told viewers could affect as many as 20 million Americans, 90 percent of them women. In the wake of the new study, Gorman said, scientists would "almost certainly" look into treating the disease with SSRIs.
  The study in question was funded by Forest Laboratories, for which Gorman has served as a consultant. A laggard in the SSRI business, the company hopes to carve out the compulsive-shopping niche for its pill, Celexa. Expect the publicity machine for something akin to "persistent purchasing disorder" to rev up soon.  What do you think?
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Offline Anonymous

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« Reply #145 on: October 04, 2004, 03:10:00 PM »
Although the grandparents did file the lawsuit it's not what you may think. The lawsuit was filed so that the grandparents would not have to spend their money prosecuting the mother. Ely Lilly will spend at least a million defending this case, and they will point the finger at mom.

Parental Alienation Syndrome was a major factor in this case. If you want more information go to
http://groups.yahoo.com/group/Lohstroh/

There is a copy of the actual suit filed along with other information. Someone is making a new web site for posting more info http://www.helpstoppas.com.
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Offline Antigen

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« Reply #146 on: October 04, 2004, 05:48:00 PM »
I wonder when they're going to come up w/ a pill for GED; generalized euphorea disorder. Ya' know, for people who, despite the economy, crime, terror alerts, perpetual war and all the rest are perversely unconcerned.

The more corrupt the state, the more numerous the laws.
http://www.amazon.com/exec/obidos/ASIN/0140440607/circlofmiamithem' target='_new'> Tacitus, Roman senator and historian (A.D. c.56- c.115)

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Offline Deborah

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« Reply #147 on: October 04, 2004, 11:38:00 PM »
In that case you would first be suspect of being a stoner. The label would come only if your piss test came out negative.
If you weren't so lucky, then you'd have to give up your illegal 'drugs' and take their mind benders. Not to worry about a label, you can walk up and spin the wheel of fortune- there are no free spots. Everybody gets a label, they don't intend to leave anyone behind.
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Hidden Lake Academy, after operating 12 years unlicensed will now be monitored by the state. Access information on the Federal Class Action lawsuit against HLA here: http://www.fornits.com/wwf/viewtopic.php?t=17700

Offline Deborah

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FDA warning on SSRIs
« Reply #148 on: October 07, 2004, 11:46:00 AM »
TONIGHT, October 07, 2004 @ 5pm Pacific Standard Time:  DANGERS OF PSYCHIATRIC DRUGS - PART 4:

Topic: ?Mental Health Screenings ? A Widespread Epidemic that MUST BE STOPPED!?   http://www.worldtalkradio.com/archive.asp?aid=2479

Tonight's AAL Show is sponsored in part by Isac Corporation and BNI - Business Network International.  
Please show your support to AAL sponsors by visiting http://www.isaccorp.org, and http://www.bni.com.  Details below.

Joining Annie Armen on AAL tonight:  

Guest Expert, Author: Fred Baughman, Jr., M.D., has been an adult and child neurologist in private practice for 35 years. Dr. Baughman has testified for victimized parents and children in ADHD/Ritalin legal cases, and writes powerful,
resourceful articles in exposing the fraud of ADD / ADHD.  
Guest Expert: Karen Effrem, M.D., - Pediatrician, researcher, conference speaker, and leading opponent of mandatory screening who serves on the boards of three national organizations: EdWatch, ICSPP, and the National Physicians Center.  
Special Guest: Patricia Weathers ? President & Founder of Ablechild.org, Parents for Label and Drug Free Education who fights for parental and children?s rights!
Guest Expert: Nathaniel S. Lehrman, M.D., a psychiatrist since 1947, is the Retired Clinical Director of Kingsboro Psychiatric Center in Brooklyn, NY and former faculty member of the Albert Einstein and Downstate Medical Schools.
« Last Edit: December 31, 1969, 07:00:00 PM by Guest »
gt;>>>>>>>>>>>>>><<<<<<<<<<<<<<
Hidden Lake Academy, after operating 12 years unlicensed will now be monitored by the state. Access information on the Federal Class Action lawsuit against HLA here: http://www.fornits.com/wwf/viewtopic.php?t=17700

Offline turbinekat

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FDA warning on SSRIs
« Reply #149 on: October 07, 2004, 01:35:00 PM »
Just curious & have been recently researching homeopathy medical practices;

DID YOU KNOW THAT...

? ADHD is a psychiatric diagnosis with no valid test to prove it exists.

? ADHD was voted into existence by a show of hands.

? Side-effects of the drugs used for ADHD include psychosis, paranoia, aggression, heart attack, cardiac arrhythmias  and high blood pressure.

? Ritalin has the same dependency profile as cocaine.

? Ritalin treatment predisposes takers to cocaine's reinforcing effects.

? The United States uses 90% of the world's Ritalin supply.

Regards,

Lee
« Last Edit: December 31, 1969, 07:00:00 PM by Guest »