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Multaq® (dronedarone) is a drug prescribed to treat irregular heart beat problems of atrial fibrillation (AF) or atrial flutter (AFL) that require hospitalization. Atrial fibrillation is an irregular heartbeat, or quivering of the heart muscle. Atrial flutter is usually associated with a rapid heartbeat. Atrial flutter can degenerate into atrial fibrillation.
Approved in July of 2009, Multaq® was the first drug to receive U.S. approval that was shown to reduce hospitalization for patients with AF or AFL.
AF is the major cause for hospitalization for heart rhythm disorders in the United States.
Major risk factors for atrial fibrillation include:
Multaq® was developed to keep the heart rhythm normal in people who have AF or AFL, which are potentially lethal heart rhythm disorders. The drug, reportedly, was considered to be one of the major innovations in treatment for AF or AFL in the last 20 years. Heart rhythm disorders combined with other risk factors lend themselves to Multaq® treatment. These are:
People who have severe heart failure or who have been recently hospitalized for heart failure, even if they are improved, should not take Multaq®, according to its manufacturer Sanofi-Aventis, an international pharmaceutical company. Multaq® can cause death in heart failure patients.
Common side effects of the drug include:
Other, more serious side effects of Multaq® are:
If you have had serious problems as a result of taken Multaq®, you should contact a Multaq® lawyer to find out if you qualify to file a lawsuit against the makers of the drug. Contact us for an evaluation of your case.
The FDA notified healthcare professionals about new findings that link Multaq® to severe liver injuries, Jan. 14, 2011. The agency said there were two report...
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