Category: Generic Drug Safety
-
When Will We Learn The Real Extent Of Generic Drug Recalls By Actavis And ETHEX
Numerous Instances Where Out-Of-Spec Oversized Pills With Double The API Dose Are Produced: How And When Did This Happen? (Posted by Tom Lamb at DrugInjuryWatch.com) In late April 2008, when the Digitek recall was announced…
-
A New “Double-Dose” Pill Drug Recall Is Issued By ETHEX Corp.
First It Was Their Morphine Tablets; Now ETHEX Dextroamphetamine 5mg Pills May Be Oversized And Contain Two Times The Active Ingredient (Posted by Tom Lamb at DrugInjuryWatch.com) By means of an October 16, 2008…
-
Congress Will Investigate Digitek Recall And What FDA Knew About Actavis Manufacturing Problems
After Earlier Class 1 Recall Of Digitek, All Acvtavis Drugs Manufactured At Its Little Falls, NJ Plant Were Recalled In August 2008 (Posted by Tom Lamb at DrugInjuryWatch.com) On October 8, 2008 Representatives John…
-
Digitek Lawsuits Filed In Federal Court Sent To The Southern District Of West Virginia
Judge Joseph R. Goodwin Will Preside Over "Double-Dose" Digitek Pill Cases Pursuant To MDL Litigation Order (Posted by Tom Lamb at DrugInjuryWatch.com) On August 13, 2008 the Judicial Panel on Multidistrict Litigation (JPMDL) issued…
-
Teva’s Budeprion XL Will Get Another Safety And Efficacy Review By FDA
FDA To Collaborate With Complaining Patients On Study Of Reported Problems With This Generic Version Of Antidepressant Wellbutrin XL (Posted by Tom Lamb at DrugInjuryWatch.com) By means of a September 23, 2008 Wall Street…