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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…
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Extent Of Digitek Recall Remains A Mystery Ten Days Later; Patients Are Left In The Dark
Heart Medication Sold By Mylan Was Made In Actavis Plant That Received FDA Letter About Manufacturing Problems Over A Year Ago (Posted by Tom Lamb at DrugInjuryWatch.com) News about the April 2008 Digitek recall…
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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…
