FDA Warns Drugmaker for Not Reporting Drug Side Effects
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FDA Warns Drugmaker for Not Reporting Drug Side Effects
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Most Recently Shared on June 15, 2010 at 10:00 am By:
FDA Warns Drugmaker for Not Reporting Drug Side Effects http://w.sns.ly/l3z46 #ED
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Higher dose of Alzheimer's drug approved despite FDA warnings, report shows - McKnight's Long Term Care News
mcknights.com — “Makers of the Alzheimer's drug Aricept released a higher dosage version of the medication despite concerns about side effects and reduced efficacy, a study reports.” View full resource at mcknights.com
Most Recently Shared on March 26, 2012 at 11:03 am By:
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Higher dose of Alzheimer's drug approved despite FDA warnings, report shows http://t.co/wZ7IlICq #alzheimer's #news
FDA issues warning on cholesterol drugs - FT.com
ft.com — “The US Food and Drug Administration has warned that cholesterol-reducing medicines sold by some of the largest drug companies can increase the risk of diabetes and memory loss. After a rise in reports of side-effects, the FDA is requiring new” View full resource at ft.com
Most Recently Shared on February 29, 2012 at 2:48 pm By:
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FDA issues warning on cholesterol drugs - http://t.co/5goEtebT - Pharmaceuticals http://t.co/mI40Gszm
Diabetes Drug Actos May Raise Risk for Bladder C... ( By Steven Reinberg HealthDay Rep...)
bio-medicine.org — “Health, By Steven Reinberg HealthDay Reporter ...THURSDAY June 16 (HealthDay News) -- The U.S. Food and Drug Administr...The agency's warning comes five days after Germany and France pulled A...The new cancer warning will appear on the labeling the FDA said. ...However although Actos does have some side effects the beneficial e...,Diabetes,Drug,Actos,May,Raise,Risk,for,Bladder,Cancer:,FDA,medicine,medical news today,latest medical news,medical newsletters,current medical news,latest medicine new” View full resource at bio-medicine.org
Most Recently Shared on June 18, 2011 at 1:14 pm By:
Diabetes Drug Actos May Raise Risk for Bladder Cancer: FDA http://bit.ly/iuGELw
Daily Diet New Warnings on Weight Loss Drugs Alli and Xenical | Health News
healthnews.com — “Consumer group Public Citizen is demanding that the FDA remove weight-loss drugs Alli and Xenical from the marketplace due to repeated reports and studies of adverse side effects to liver, kidneys and pancreas.” View full resource at healthnews.com
Most Recently Shared on April 15, 2011 at 4:13 pm By:
Daily Diet: New Warnings on Weight-Loss Drugs Alli and Xenic http://ht.ly/4B9fL
FDA cites Sanofi over drug side effect reporting | Reuters
reuters.com — “WASHINGTON (Reuters) - The Food and Drug Administration warned Sanofi-Aventis SA's U.S. unit for failing to tell the agency about reports of possible serious side effects in a timely manner.In a January” View full resource at reuters.com
Most Recently Shared on February 22, 2011 at 4:40 pm By:
FDA cites Sanofi over drug side effect reporting http://reut.rs/fNpXnx
UPDATE 2-FDA cites Sanofi over drug side effect reporting | Reuters
reuters.com — “* Agency says warning follows 2010 inspection * Sanofi's response, plan to fix problem 'inadequate' -FDA * Sanofi pledges to work with FDA * Shares down 2.7 percent WASHINGTON, Feb 22 (Reuters)” View full resource at reuters.com
Most Recently Shared on February 22, 2011 at 4:33 pm By:
Susan Heavey Health Communicator
Sanofi $SNY on receiving end of not 1 but 2 recent warning letters released by FDA today: http://link.reuters.com/neq28r
FDA cites Sanofi over drug side effect reporting
health.yahoo.net — “The Food and Drug Administration warned Sanofi-Aventis SA's U.S. unit for failing to tell the agency about reports of possible serious side effects in a timely manner.” View full resource at health.yahoo.net
Most Recently Shared on February 22, 2011 at 4:30 pm By:
Jane Anderson Healthy Eating Advisor
FDA cites Sanofi over drug side effect reporting http://bit.ly/fLJqf3
FDA and Depakote Birth Injury Resources Warn of Increased Risk of Birth Defects in Babies Exposed to Valproate Sodium During Pregnancy
prweb.com — “The US Food and Drug Administration has issued a warning to health care professionals and patients about the potential increased risk of birth injuries and birth defects when valproate sodium and related products (e.g. Depacon, Depakote or Stavzor) are used by mothers during pregnancy. Depakote Birth Injury Resources (DepakoteBirthInjury.com) offers information and resources about the possible side effects of valproate sodium, including neural tube malformations, craniofacial defects and cardiov” View full resource at prweb.com
Most Recently Shared on December 5, 2010 at 1:54 am By:
Depakote and birth injuries according to FDA report http://bit.ly/fndQ95
Malaria Drug Should Not be Used to Treat Leg Cramps - FDA Warning
disabled-world.com — “Serious side effects reported when used to treat or prevent night time leg cramps” View full resource at disabled-world.com
Most Recently Shared on July 8, 2010 at 8:04 pm By:
Disabled World Health Advocate and Health News
Malaria Drug Should Not be Used to Treat Leg Cramps - FDA Warning http://ff.im/-nqjqQ
FDA warns Pfizer for not reporting side effects: WASHINGTON (Reuters) - The U.S. Food and Drug Administration has ... http://bit.ly/9wwTFC
reuters.com — “FDA warns Pfizer for not reporting side effects: WASHINGTON (Reuters) - The U.S. Food and Drug Administration has ... http://bit.ly/9wwTFC” View full resource at reuters.com
Most Recently Shared on June 10, 2010 at 12:18 pm By:
FDA warns Pfizer for not reporting side effects: WASHINGTON (Reuters) - The U.S. Food and Drug Administration has ... http://bit.ly/9wwTFC
LASIK: Quality of Life Project, Warning Letters to Facilities
fda.gov — “On October 15, 2009, the U.S. Food and Drug Administration (FDA) launched a study of the impact of LASIK on patients' quality of life, and issued warning letters to 17 LASIK surgery centers that release patients the same day as their surgery.” View full resource at fda.gov
Most Recently Shared on October 21, 2009 at 11:05 pm By:
17 LASIK eye surgery centers get warning letters after #FDA finds inadequate system for reporting #health side-effects http://ow.ly/vLji
Tamiflu And Relenza Should Have Psychiatric Side Effects Warning, Say Regulators
medicalnewstoday.com — “After receiving reports of patients experiencing delirium, psychosis and hallucinations, US FDA staff recommend that flu drugs, Tamiflu and Relenza should carry warnings about possible side-effect” View full resource at medicalnewstoday.com
Most Recently Shared on April 28, 2009 at 2:19 am By:
William Yates, M.D. Doctor, Psychiatrist, Family Medicine Doctor, and Physician
RT @larrybrauner: Never simple! "Tamiflu And Relenza Should Have Psychiatric Side Effects Warning, Say Regulators" http://budurl.com/j93s
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FDA Warns Drugmaker for Not Reporting Drug Side Effects http://w.sns.ly/r3x44
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