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If you or someone you love has been harmed by the drug Multaq®, you might be eligible for compensation. To find out if you qualify to file a Multaq® lawsuit, please contact us today.
If you or someone you love has suffered from severe liver damage after taking Multaq® (dronedarone), you should contact an attorney to discuss your options for a lawsuit against the drug manufacturer. It is known that at least two patients who took Multaq® went into liver failure and required a liver transplant.
Contact a Multaq® lawyer today.
Multaq® is prescribed to treat heart patients who have atrial fibrillation or atrial flutter. Both are types of heart rhythm abnormalities. The medication is made by the French drug company Sanofi-Aventis.
If you believe you have liver damage you may notice some signs of the disease, which include the following:
Multaq® , known by its generic name dronedarone, was approved by the U.S. Food and Drug Administration (FDA) on July 2, 2009. As a requirement for the drug's approval, its manufacturer had to add a black box warning to the drug's label. A black box warning is the most serious warning a drug label can have.
The black box warning said the drug was contraindicated (not to be used) in patients with severe heart failure. A study of patients who had severe heart failure or were recently hospitalized for heart failure showed that those patients given Multaq® had more than twice the risk of dying.
If someone you love was in severe heart failure and died after taking Multaq®, you may have grounds for a lawsuit. Contact a Multaq® attorney to talk about what your options for a lawsuit might be for the loss of a loved one.
If you have the following symptoms, you may be experiencing congestive heart failure:
If you or someone you love has suffered damage to your liver or your heart after taking Multaq® , you should contact a Multaq® injury lawyer. You and you lawyer can discuss your options for a lawsuit against the drug company for seriously harming your life.
Please contact us today to schedule 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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