Pradaxa (dabigatran etexilate mesylate) is a blood thinning medication used to reduce the risk of stroke or serious blood clots in patients with non-valvular atrial fibrillation, the most common type of heart rhythm abnormality. Pradaxa was approved by the U.S. Food and Drug Administration in October 2010. Pradaxa is manufactured by Boehringer Ingelheim Pharmaceuticals, Inc.
A new study released January 9 found that Pradaxa carries an increased risk of heart attack compared with other anti-coagulant medications. The study found that patients taking Pradaxa have a 33% higher relative risk of heart attack or severe symptoms of heart disease than do patients taking other common treatments.
The FDA is also investigating reports of serious bleeding events in patients taking Pradaxa. Case reports on Pradaxa have noted increased bleeding associated with advanced age, renal impairment, and low body weight. Bleeding can lead to serious injury or even fatal outcomes. Bleeding may be a complication of anticoagulant therapies. However, the FDA is working to determine whether the reports of bleeding in patients taking Pradaxa are occurring more commonly than would be expected. 
Robins Kaplan Miller and Ciresi LLP is investigating Pradaxa. If you or someone you know has been injured or killed following use of Pradaxa and you wish to consult with a lawyer, please call us at 1-800-553-9910 or e-mail us by clicking on this link: contact us.
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