Medication Safety

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OTC Heartburn Medication Recalled
Sanofi-Aventis US issued a precautionary, voluntarily recall of all over-the-counter Zantac (ranitidine) products because of possible contamination with NDMA.
Antiarrhythmic Agent Recalled
The FDA has issued a recall for a prescription antiarrhythmic used to treat heart rhythm issues.
Additional Antacids Pulled Over NMDA Contamination
AvKARE Inc. and AuroMedics Pharma have joined a number of companies voluntarily recalling ranitidine products because of contamination with the probable human carcinogen N-Nitrosodimethylamine.

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OTC Heartburn Medication Recalled
Antiarrhythmic Agent Recalled
Additional Antacids Pulled Over NMDA Contamination
Liquid Pain Medicine Recalled in Three States
Seizure Med Recalled
Antiviral Drug Recalled
Acne Med Recalled
Antacid Recall Grows
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