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FDA Issues New Warning For the Drugs Multaq Following Results of Study


The U.S. Food and Drug Administration has completed a safety review of the heart drug dronedarone trade name Multaq. The results showed an increased risk of cardiovascular issues including death with patients in permanent atrial fibrillation. The FDA is recommending a new warning label on the prescription medication to indicate the heightened risk.

Commentary

Atrial fibrillation is a cardiac arrhythmia (or abnormal heartbeat) developed in the upper two chambers of the heart. Some who suffer from an irregular heartbeat actually do not experience symptoms (other than the skipping beat) while others need medication for the discomfort they endure. My readers who fall into the latter category should be cautious and potentially consult their doctor if they are currently taking Multaq. The FDA advises if atrial fibrillation (AF) is permanent in other words chronic irregular heartbeats stop use.

Texas Drug Injury Attorney Michael Grossman

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