Exposing Psychology, Exalting Christ

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FDA approves Abilify for bipolar children, despite major known health risks
 

ALLIANCE FOR HUMAN RESEARCH PROTECTION

Promoting Openness, Full Disclosure, and Accountability

http://www.ahrp.org and http://ahrp.blogspot.com

 

FYI

Will somebody stop the FDA from approving chemical weapons of destruction

aimed at America's children?

 

The documented, demonstrable risks of severe harm produced by the second

generation antipsychotic drugs is uncontestable.

Even leading schizophrenia researchers with financial ties to manufacturers,

such as Dr. Jeffrey Lieberman, chairman of psychiatry at Columbia

University, acknowledge:

``The major problem with second-generation antipsychotic drugs is weight

gain and diabetes. `The younger you are, the more severe and common these

side effects.''

 

Despite the severity of the risks, and despite the lack of evidence of a

therapeutic benefit, the FDA has just approved Abilify for use in children

for "bipolar" disorder, which is the "diagnosis" du jour for bad behavior.

The FDA once again, acted irresponsibly, lending the government seal of

approval without so much as a public hearing! The FDA approval of Risperdal

for children was similarly meted out.

See new Abilify label:

http://www.fda.gov/cder/foi/label/2008/021436s21,021713s16,021729s8,021866s8

lbl.pdf

 

The FDA seems to have launched an undeclared War on America's children whose

mental and physical health are being jeopardized to increase profits and

shield companies from illegal off-label promotion of the most toxic drugs

used for non-life-threatening disease.

 

Congressional action is urgently to stop the catastrophic consequences.

 

 

Contact: Vera Hassner Sharav

veracare@ahrp.org

212-595-8974

 

 

http://www.bloomberg.com/apps/news?pid=conewsstory&refer=conews&tkr=BMY:US&s

id=aTSROCE31mzs

BLOOMBERG NEWS

Bristol-Myers Drug Cleared to Treat Pediatric Bipolar

By Beth Jinks

 

Feb. 28 (Bloomberg) -- Bristol-Myers Squibb Co.'s antipsychotic medicine

Abilify was cleared by U.S.

regulators to treat bipolar disorder in children as young as 10.

 

The U.S. Food and Drug Administration approved the added use for the pill,

the agency said today in new prescribing information posted on its Web site.

Abilify is already marketed for adults with bipolar disorder and major

depression, and for schizophrenia in people 13 and older.

 

Sales of Abilify, the New York-based company's second-best seller, climbed

29 percent to $1.66 billion last year, helped by studies showing it caused

less weight gain than competing treatments. The only other drug in the class

known as atypical antipsychotics that is approved to treat bipolar disorder

in children 10 and older is Johnson & Johnson's top-selling Risperdal, which

won U.S. clearance for that use in August.

 

Abilify offers a potential advantage over other atypical antipsychotics

because ``it doesn't cause to the same degree weight gain and metabolic''

disorders, said Jeffrey Lieberman, chairman of psychiatry at Columbia

University in New York, in a telephone interview yesterday.

 

``The major problem with second-generation antipsychotic drugs is weight

gain and diabetes,'' Lieberman said.

 ``The younger you are, the more severe and common these side effects.''

 

Rising Diagnosis

The number of American children diagnosed with bipolar disorder, once known

as manic depression, jumped 40-fold from 1994 to 2003, according to a study

in the Archives of General Psychiatry released in September.By 2003, the

diagnosis was applied to 1 in 100 kids, researchers found.

 

Bristol-Myers fell 29 cents, or 1.3 percent, to $22.91 at 4:17 p.m. in New

York Stock Exchange composite trading. The company has dropped 13 percent in

12 months.

 

>From 2003 to 2006, U.S. prescriptions for Abilify for children 18 years and

younger soared sevenfold to more than 1 million, according to data from

Wolters Kluwer NV, a drug- tracking company. Doctors can prescribe medicines

for uses not approved by the FDA, such as using Abilify in young children,

although drugmakers can't market their products for such ``off- label''

purposes.

 

``It wasn't well-recognized before, and in all candor there's probably an

over-diagnosis,'' Lieberman said.

``There's some fuzziness around the diagnosis which leads to some children

believed to have bipolar disorder, who don't turn out to have it when they

grow up.''

 

`Be Judicious'

Doctors need to be ``very judicious in their use of these drugs,''

particularly in children, Lieberman said.

 

Adults with bipolar disorder often stay lodged for weeks or months in states

of deep depression, then shift to a manic phase in which they sleep little,

have intense energy, talk rapidly, and may engage in risky behavior.

 

Some psychiatrists say the disorder looks different in children, who may

alternate more rapidly between depression and mania, or demonstrate

moodiness, irritability and volatility. The condition has been linked to

poor school performance and substance abuse.

 

In November, Abilify was cleared by U.S. regulators to treat adults with

severe depression, and for use by teens with schizophrenia. The drug was

first approved in 2002 to treat adult schizophrenia, a condition that causes

distorted thinking, hallucinations and an inability to feel normal emotions.

 

`Evidence of Commitment'

``The approval is one of a series we've had for Abilify in a short amount of

time,'' Sonia Choi, a Bristol-Myers spokeswoman, said in a phone interview.

``This is evidence of our commitment to developing medicines to their full

potential.''

 

Abilify is second among Bristol-Myers' products to the blood-thinner Plavix,

which had $4.76 billion in sales last year.

 

Antipsychotic drugs reduce levels of dopamine, a brain chemical that, in

excess, is thought to cause symptoms of psychosis and mania.

 

Atypical psychotics, which include Abilify, Risperdal and Eli Lilly & Co.'s

Zyprexa, first came on the market in the mid- 1990s. The products were

marketed as causing fewer of the neurological side effects that made users

of earlier medications, such as Haldol and Thorazine, tremble, doze off and

jerk involuntarily.

 

Seroquel and Geodon

Other antipsychotics include AstraZeneca Plc's Seroquel and Pfizer Inc.'s

Geodon. Bipolar disorder is often also treated with anticonvulsants,

developed to treat epileptic seizures.

 

Lilly's request to sell Zyprexa to treat schizophrenia and bipolar disorder

in teenagers was delayed by the FDA in April. Lilly received what the FDA

calls an approvable letter, indicating the agency needs more time to analyze

data and to determine the drug's prescribing information.

 

``We don't have a time frame at this point,'' Lilly spokeswoman Marni Lemons

said in a phone interview.

``We have no intention for promoting the drug for use in adolescents. We

want to add information to the label.''

 

J&J reported $4.7 billion in revenue from anti-psychotic medicines including

Risperdal last year, up 12 percent from 2006. The company doesn't report

separate sales figures for Risperdal.

 

Bristol-Myers and Tokyo-based Otsuka Pharmaceutical Co. said Nov. 15 they

had won priority FDA review of a study testing Abilify on patients 10 to 17

years old diagnosed with bipolar disorder. Priority review speeds up the

approval process, which typically takes about six months with pediatric

medicines.

 

Otsuka discovered Abilify and retains marketing rights to the drug in Japan

and some other Asian markets.

 

Europe's Committee for Medicinal Products for Human Use recommended Feb. 22

that Abilify be approved to treat bipolar disorder. The drug was approved by

the European Commission as a schizophrenia treatment in Europe in 2004.

 

To contact the reporter on this story: Beth Jinks in New York at

bjinks1@bloomberg.net

Last Updated: February 28, 2008 17:36 EST

 

 

 

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Copyright © 2002 - 2007 Lisa & Ryan Bazler

P.O. Box 864, Cardiff, CA 92007 

lisaandryan@psychologydebunked.com

Last updated: 03/25/2008

 

Note: The mission of this ministry is to inform mental sufferers and those from whom they seek help of the physical, mental and spiritual dangers of mental health disorders and treatments, and to encourage them to pursue a drug-free, psychology-free, Christ-centered life.  Visitors to this web site taking psychotropic drugs who wish to discontinue use are strongly advised to consult a qualified physician for assistance and supervision before starting the discontinuation process. This ministry and web site provides information to help visitors make the most informed decisions about their mental health, and should not replace the advice of a medical doctor.