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FDA Says It Doesn’t Know How Long Defective Digitek / Digoxin Pills Were Sold
Actavis Says They Have Received 11 Complaints About Digitek Side Effects That Date Back To 2006 (Posted by Tom Lamb at DrugInjuryWatch.com) The facts surrounding a late April 2008 recall of Digitek (digoxin) pills…
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Digitek Digoxin Recall: Tablets May Be Double The Normal Dose
So-called "Digitalis Toxicity" Is Possible, Especially In Patients With Renal Failure (Posted by Tom Lamb at DrugInjuryWatch.com) In an April 28, 2008 MedWatch Safety Alert about Digitek (digoxin tablets), the FDA informed doctors and…
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FDA’s 2007 Report On Outstanding Post-approval Studies: No Progress Made By Big Pharma
After Their Medications Get Approved By FDA, Many Drug Companies Have Not Yet Started The Studies Which They Promised To Do (Posted by Tom Lamb at DrugInjuryWatch.com) Each year the FDA issues what could…
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April 2008 Accutane Trial In New Jersey Ends With Plaintiff Verdict
Utah Woman Developed Inflammatory Bowel Disease After Using This Hoffman-LaRoche Drug (Posted by Tom Lamb at DrugInjuryWatch.com) _____________________________________________________________________ Update: Roche Wins Reversal of $10.5 Million Accutane Verdict in New Jersey Case By Jef Feeley…
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April 2008: FDA Web Site Adds Two New Pages For Learning About Drug Safety
Some Important Terms Are Defined And Various Research Resources From FDA Are Listed (Posted by Tom Lamb at DrugInjuryWatch.com) On April 11, 2008 the FDA added to its web site one page that gives…
