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8/10/2011
Zimmet & Quarles
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Tip Of The Day | Atrial Fibrillation Drug Multaq and FDA Warning | Florida Medical Malpractice Attorney


If you're taking the atrial fibrillation drug Multaq, the FDA wants you to call your doctor right away.

Don't stop taking the drug -- that could be dangerous. But the FDA wants patients to be aware that a clinical trial of Multaq, called PALLAS, was halted when the drug doubled the risk of death, stroke and heart failure hospitalization in heart patients with permanent atrial fibrillation.

Multaq is approved to treat paroxysmal atrial fibrillation (intermittent), persistent atrial fibrillation, or atrial flutter. The big question -- now the subject of an FDA investigation -- is exactly how the PALLAS findings apply to current patients. Multaq was approved in 2009 after the ATHENA clinical trial showed it decreased deaths in patients with non-permanent atrial fibrillation and atrial flutter.  But this is now the fifth time the FDA has reported signals of possible risk from Multaq.


Category: Medical Malpractice


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Zimmet & Quarles. P.L.
Halifax Harbor Marina
125 Basin Street, Suite 210
Daytona Beach, FL 32114
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Zimmet & Quarles. P.L.
Halifax Harbor Marina
125 Basin Street, Suite 210
Daytona Beach, FL 32114
Phone: (386) 255-4020
Fax: (386) 255-2027
Toll Free: (800) 934-1020

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