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If you or a loved one has experienced Multaq® liver toxicity or acute liver failure, contact an attorney for dangerous drugs. We may be able to help you seek and recover compensation for your injury and loss.

Multaq® Liver Toxicity: Background

The U.S. Food and Drug Administration (FDA) announced that Multaq® (dronedarone) might be linked to liver toxicity and acute liver failure. The agency is adding a liver toxicity warning to the drug's label to warn patients and healthcare providers about the potential risk of liver damage.

According to the FDA, several patients have reported liver problems within six months of taking Multaq®. Two patients needed liver transplants following acute liver failure. One of the patients suffered liver failure after 4.5 months of starting a Multaq® treatment and the other suffered liver failure in about six months after initial treatment, says the FDA.

Multaq® has been available since July 2009.

Liver Damage Related to the Multaq® Drug

When a prescribed medication such as Multaq® causes liver damage to a patient, it is known as drug-induced liver injury. The liver is a vital organ that has many functions. When the liver is damaged by Multaq® or other drugs, it cannot function properly.

Patients might experience symptoms such as:

• Jaundice (yellowing of the skin and eyes)
• Nausea
• Vomiting
• Fatigue
• Abdominal pain

Multaq® liver toxicity can lead to hospitalization, infection, disability and life threatening liver failure.

Multaq® Liver Injury: Data Summary

In the FDA's notification, the agency said it received two reports of acute hepatic failure cases that required liver transplants. According to data, both patients were about 70 years old and female.

One of the patients was prescribed Multaq® for the treatment of underlying intermittent atrial fibrillation, arterial hypertension and stable coronary artery disease. She took Multaq® for 4 and a half months before suffering liver failure. About one week before being admitted to the hospital, the patient complained of extreme exhaustion. According to reports, she stopped taking dronedarone just before being admitted to the hospital.

In another case, the patient began reporting symptoms, including stomach pains, weakness and hyperbilirubinemia after six months of taking dronedarone. She received a liver transplant one month later.

Contact a Multaq® Liver Injury Lawyer

If you are taking Multaq®, it is important to understand the symptoms of liver failure. Seek medical attention immediately if you begin to feel overly tired, pains in the stomach, unexplained nausea, or other unusual symptoms.

If you are diagnosed with liver toxicity, you should also be aware of your legal rights. To find out if you are eligible to recover compensation for your injury, contact our Multaq® liver injury attorneys today.

"FDA Alert: Multaq® Linked to Liver Failure"

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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