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Documents 1-15 out of 15 found
  Current Search:  mellaril: 15     

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FDA Orders New Boxed Warnings On Antipsychotic Drugs Labels
Nidhi Sharma - AHN News Writer Washington D.C.

(AHN) - The U.S.

Food and Drug Administration is ordering manufacturers of antipsychotic drugs to include boxed warnings on the products after the agency found that the medications can...

All Headline News:  Jun 17 2008 4:05PM
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U.S. FDA expands antipsychotic drug warning
WASHINGTON (Reuters) - Older, conventional antipsychotic medications should carry a 'black box' warning about an increased risk of death in some elderly people being treated for dementia-related psychosis, the U.S.

Food and Drug...

Canada.com:  Jun 17 2008 11:05AM
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FDA warns schizophrenia drugs pose fatal risk to some seniors
WASHINGTON (AP) - The government is warning doctors that prescribing a certain group of psychiatric drugs to seniors suffering from dementia can increase their risk of death.

Anti-psychotic drugs are approved to treat schizophrenia and...

WCPO:  Jun 17 2008 4:09AM
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FDA warns schizophrenia drugs pose fatal risk to some seniors
s/File) WASHINGTON (AP) - The government is warning doctors that prescribing a certain group of psychiatric drugs to seniors suffering from dementia can increase their risk of death.

Anti-psychotic drugs are approved to treat schizophrenia...

KEYE Austin:  Jun 17 2008 3:35AM
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U.S. FDA expands antipsychotic drug warning
WASHINGTON (Reuters) - Older, conventional antipsychotic medications should carry a 'black box' warning about an increased risk of death in some elderly people being treated for dementia-related psychosis, the U.S.

Food and Drug...

Scientific American:  Jun 17 2008 1:31AM
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U.S. FDA expands antipsychotic drug warning
WASHINGTON (Reuters) - Older, conventional antipsychotic medications should carry a 'black box' warning about an increased risk of death in some elderly people being treated for dementia-related psychosis, the U.S.

Food and Drug...

Reuters UK:  Jun 17 2008 1:18AM
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U.S. FDA expands antipsychotic drug warning (Reuters)
The older drugs include Pfizer Inc's Navane, Johnson & Johnson's Haldol, and Endo Pharmaceutical Holdings Inc's Moban, according to a database on the FDA's website.

It was not immediately clear which drugs were still on the market, and...

Yahoo!:  Jun 17 2008 1:08AM
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UPDATE 2-U.S. FDA expands antipsychotic drug warning
WASHINGTON, June 16 (Reuters) - Older, conventional antipsychotic medications should carry a 'black box' warning about an increased risk of death in some elderly people being treated for dementia-related psychosis, the U.S.

Food and Drug...

Reuters:  Jun 17 2008 1:03AM
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U.S. FDA expands antipsychotic drug warning
WASHINGTON (Reuters) - Older, conventional antipsychotic medications should carry a 'black box' warning about an increased risk of death in some elderly people being treated for dementia-related psychosis, the Food and Drug Administration...
Forbes.com:  Jun 17 2008 12:55AM
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FDA warns schizophrenia drugs pose fatal risk to some seniors
Conventional Antipsychotic Drugs Atypical Antipsychotics Compazine (prochlorperazine) Abilify (aripiprazole) Haldol (haloperidol) Clozaril (clozapine) Loxitane (loxapine) FazaClo (clozapine) Mellaril (thioridazine) Geodon (ziprasidone)...
NewsChannel 9 WSYR:  Jun 17 2008 12:30AM
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FDA wants warnings on antipsychotic drugs
WASHINGTON, June 16 (UPI) -- The U.S.

Food and Drug Administration says it is ordering manufacturers of 'conventional' antipsychotic drugs to include boxed warnings on the products.

The FDA said it will require pharmaceutical companies...

UPI:  Jun 16 2008 9:54PM
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Lilly Submits Cymbalta(R) Supplemental New Drug Application for Chronic Pain to U.S. Food and Drug Administrat
INDIANAPOLIS, May 29 (HSMN NewsFeed) -- Eli Lilly and Company (NYSE: LLY ) has submitted a supplemental New Drug Application (sNDA) to the U.S.

Food and Drug Administration (FDA) seeking approval for a new indication for Cymbalta ...

Healthcare Sales & Marketing Network:  May 30 2008 8:07PM
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Lilly Submits Cymbalta® Supplemental New Drug Application For Chronic Pain To U.S. Food And Drug Administr
Eli Lilly and Company has submitted a supplemental New Drug Application (sNDA) to the U.S.

Food and Drug Administration (FDA) seeking approval for a new indication for Cymbalta (duloxetine HCl) for the management of chronic pain, the...

Pharmaceutical Online:  May 30 2008 6:03AM
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Lilly Submits Cymbalta(R) Supplemental New Drug Application for Chronic Pain to U.S. Food and Drug Administrat
Eli Lilly and Company (NYSE: LLY) has submitted a supplemental New Drug Application (sNDA) to the U.S.

Food and Drug Administration (FDA) seeking approval for a new indication for Cymbalta?

(duloxetine HCl) for the management of chronic...

TMC Net:  May 29 2008 3:50PM
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LILLY (ELI) & COMPANY: Lilly Submits Cymbalta Supplemental New Drug Application
For Release: 8:00 AM Eastern Time Refer to: Charlie McAtee Sonja Popp-Stahly 317-277-1566 (office) 317-655-2993 (office) 317-997-1627 (mobile) 317-437-9947 (mobile) mcatee_charles@lilly.com spopp-stahly@lilly.com Lilly Submits Cymbalta...
FinanzNachrichten.de:  May 29 2008 12:39PM
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