A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: Multaq (dronedarone): Drug Safety Communication – Increased Risk of Death or Serious Cardiovascular Events. According to the Food & Drug Administration FDA’s MedWatch:
UPDATED 12/19/2011. FDA completed safety review, issued new recommendations. Originally posted 07/21/2011
For more information on the drug or medical device recall or safety alert, read the Food & Drug Administration’s FDA’s drug or medical device recall or safety alert: Multaq (dronedarone): Drug Safety Communication – Increased Risk of Death or Serious Cardiovascular Events.
To report an adverse reaction, problem or other issue with a drug or medical device, submit a drug or medical device complaint to the government at fda.gov or MedWatch.
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