16 October 2015 - The U.S. Food and Drug Administration today granted accelerated approval to Praxbind (idarucizumab) for use in patients who are taking the anticoagulant Pradaxa (dabigatran) during emergency situations when there is a need to reverse Pradaxa’s blood-thinning effects.

For more details, go to: http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm467300.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery