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Actavis And FDA Criticized Over Their Digitek Recall Conduct In New 2009 Report
ISMP QuarterWatch: Cannot "rule out, or state definitively, whether defective digoxin tablets led to hundreds of patient deaths" (Posted by Tom Lamb at DrugInjuryWatch.com) On January 15, 2009 The Institute for Safe Medication Practices…
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Celgene Letter About Revlimid And Serious Skin Reactions In January 2009 Medical Journal
Discusses 16 Cases Of Stevens-Johnson Syndrome (SJS), Toxic Epidermal Necrolysis (TEN), and Erythema Multiforme (EM) Reported Over Two-and-a-half Years (Posted by Tom Lamb at DrugInjuryWatch.com) In an October 1, 2008 article, "FDA Alerts Doctors…
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All Sprint Fidelis Federal Court MDL Cases Dismissed On Federal Preemption Grounds
U.S. District Court Judge in Minnesota Follows Supreme Court's Riegel vs. Medtronic Ruling As Precedent In Making His January 2009 Ruling (Posted by Tom Lamb at DrugInjuryWatch.com) All of the Sprint Fidelis cases that are…
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Digitek Update December 2008: Actavis Contends No Defective Digitek Pills Were Ever Used By Patients
At About Same Time, Drug Company Accepts FDA Consent Decree In Connection With Justice Department's Injunction Complaint (Posted by Tom Lamb at DrugInjuryWatch.com) In late December 2008 investigative reporter Jeanne Lenzer's hard-hitting article about…
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ETHEX Recalls One Lot Of Hydromorphone HCl (2mg) After Finding Oversized Tablet
At Same Time, KV Pharmaceutical Suspends Shipments of All ETHEX Tablet-Form Drugs For An Indefinite Period (Posted by Tom Lamb at DrugInjuryWatch.com) On December 23, 2008 KV Pharmaceutical announced another drug recall involving its…
