Following the March 23-26 meetings of the European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP), outcomes of reviews on three groups of medicines have been announced. These are as follows:
Outcome of review on direct oral anticoagulants
No change to the conditions of use of the direct oral anticoagulants Eliquis (apixaban), from New York-based pharma majors Bristol-Myers Squibb (NYSE: BMY) and Pfizer (NYSE: PFE), Pradaxa (dabigatran etexilate), from Germany’s Boehringer Ingelheim, and Xarelto (rivaroxaban), from German major Bayer (BAYN: D) is needed following a review of the results of a European study of real-world data for these medicines.
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