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Actavis Tells Us More, But Not Much More, About April 2008 Digitek Recall
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 (Posted by Tom Lamb at DrugInjuryWatch.com) On May…
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FDA Safety Evaluation Of Antibiotic Maxipime Is Not Completed, Yet
Six Months After It Announced Start Of This Investigation, FDA Gives An Update On Status Of Maxipime Safety Review (Posted by Tom Lamb at DrugInjuryWatch.com) In mid-November 2007 the FDA announced the start of…
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May 2008 Update: Sprint Fidelis Lead Wire Failures Due To Design Flaw, Not Doctors
Medtronic Had Initially Suggested That It Was Implant Technique That Caused The Sprint Fidelis Malfunctions (Posted by Tom Lamb at DrugInjuryWatch.com) For today’s post we have to thank Westby G. Fisher, MD, FACC, who…
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May 2008 Congressional Hearing On Federal Preemption Of Drug And Medical Device Lawsuits
Committee Will Hear From A Diverse Set Of Witnesses On The Various Aspects Of This Controversial Legal Doctrine (Posted by Tom Lamb at DrugInjuryWatch.com) On May 14, 2008 the House of Representative’s Committee on…
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Recall Notice For Digitek Marketed Under Bertek Label Goes Back To March 2006
North Carolina Board Of Pharmacy Has Posted A Copy Of The Bertek Digitek Drug Recall Notice On Its Web Site (Posted by Tom Lamb at DrugInjuryWatch.com) The home page of the North Carolina Board…
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Ortho Evra Recall Requested By Public Citizen Due To Blood Clot Risks
Women Have Developed Serious Side Effects Like Deep Vein Thrombosis (DVT) and Pulmonary Embolism (PE) After Using This Birth Control Patch (Posted by Tom Lamb at DrugInjuryWatch.com) On May 8, 2008 Public Citizen’s Health…