Search results for drug-injury

On April 11, 2008 the FDA added to its web site one page that gives short definitions for some important terms used in the realm of prescription drug safety, and another page that is intended to assist one when researching medication safety issues. read more »
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Utah Woman Developed Inflammatory Bowel Disease After Using This Hoffman-LaRoche Drug read more »
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In an April 28, 2008 MedWatch Safety Alert about Digitek (digoxin tablets), the FDA informed doctors and patients that this prescription medication is the subject of a nationwide Class I recall. 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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On May 14, 2008 a House of Representative's Committee will convene a hearing to explore the legal doctrine of federal preemption in the context of product liabilitliability lawsuits involving FDA-approved drugs and medical devices. 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 back in 2006 read more »
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Recall Now Covers 30 mg And 60 mg Tablets Made During June 2006 To May 2008 Period Due To The Potential For Oversized Tablets read more »
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June 2008 Staff Report Cites Cancers, Infections, And Neurological Problems Similar To Serious Side Effects In Adults read more »
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Beware If Taking This Seizure Medicine Alone Or With Other Epilepsy Drugs During Pregnancy read more »
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Risk Of Adverse Hepatic Reactions, Including Fatal Liver Injury, Is Cited by European Regulators At July 2008 Meeting read more »
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August 2008 Counterpart of HR 6381, Medical Device Safety Act 2008, Which Was Sponsored By Congressmen Waxman And Pallone read more »
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Most Of These Product Liability Cases Allege Fosamax Caused Drug-Induced Osteonecrosis Of The Jaw (ONJ) read more »
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