Search results for drug-safety

On March 31, 2008, at the American College of Cardiology's annual meeting, a recent analysis of several studies involving Pfizer Inc.'s arthritis drug Celebrex was presented. read more »
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The FDA added a page that gives definitions for some important terms used in the realm of prescription drug safety, and a page that is intended to assist one when researching medication safety issues read more »
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Each year the FDA issues a so-called "report card" on how the pharmaceutical companies are doing as regards post-approval studies for their products that have been approved for sale in the U.S. read more »
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The facts surrounding the late April 2008 recall of Digitek (digoxin) pills that may have twice the active ingredient is becoming less clear as we learn more in the days following the FDA recall. read more »
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Heart Medication Sold By Mylan Was Made In Actavis Plant That Received FDA Letter About Manufacturing Problems Over A Year Ago read more »
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North Carolina Board Of Pharmacy Has Posted A Copy Of The Bertek Digitek Drug Recall Notice On Its Web Site read more »
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Six Months After It Announced Start Of This Investigation, FDA Gives An Update On Status Of Maxipime Safety Review read more »
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Actavis, Mylan, Or The FDA Should Tell Public Their Current Estimate Of How Many Defective Digitek Pills Were Distributed To Pharmacies, And During What Time Period read more »
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A study published in June 2008 by the Canadian Medical Association Journal which concerned 1,017 patients who presented at the Vancouver General Hospital emergency room (ER) during a 12-week period ba... read more »
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The FDA has started an investigation into the potential link between certain TNF blockers used to treat Juvenile Idiopathic Arthritis (JIA), Crohn’s disease, or other diseases and the development of read more »
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