Search results for recall

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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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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October 2008 Public Citizen Petition Wants Glaxo's Diabetes Drug Banned Due To "New" Side Effect, Liver Toxicity read more »
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Researchers Looked For Possible Digoxin Related Adverse Drug Events In Older Patients From Pennsylvania read more »
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Related Recall Of Over-The-Counter OSP Fleet Phospho-soda Product That Is Subject Of Product Liability Lawsuits read more »
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At Present, This March 2009 Recall Is Limited To Propafenone HCL 225 mg Tablets Shipped Between October 15, 2008 And November 26, 2008 read more »
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Digitek Brand Of Generic Digoxin Tablets Had Been Recalled In April 2008 For Same Reason read more »
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Reports Made To The FDA Have Involved Hepatitis, Liver Failure, Liver Transplant, And Death read more »
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Difference Of Opinion Suggests There Could Be A Possible Meridia Recall In U.S. Before The FDA Holds Its Public Advisory Meeting In September 2010 read more »
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