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Sep 21, 2015 · EU approved the very first NOAC (or novel oral anticoagulant) Xarelto (rivaroxaban) for broad application With Bayer and Janssen at the helm, Xarelto can now be broadly used for patients suffering from atrial fibrillation (AF) Oct 28, 2008 · The European Commission has granted marketing approval to the Bayer Group for Xarelto (rivaroxaban), an anticoagulant taken as one tablet, once-daily, to prevent venous thrombo-embolic events (VTE) in adults undergoing elective (planned) hip or knee replacement surgery List of Marketing Authorisations (MA) containing Xarelto registered and approved in Europe on PharmaCompass comThe below overview respresents the approval status of Xarelto in the European Union (as approved by EMA) Doctors should always refer to their local product information for further detail on approved indication in their country May 24, 2013 · The European Commission approved the oral anticoagulant rivaroxaban for the prevention of atherothrombotic events after an acute coronary syndrome (ACS) in adult patients with elevated cardiac biomarkers This website contains information on Xarelto (rivaroxaban) which is based on the Summary of Product Characteristics (SPC) as approved by the European Commission Nov 20, 2012 · The European Commission has approved the oral anticoagulant rivaroxaban for the treatment of pulmonary embolism (PE) and the prevention of recurrent deep vein thrombosis (DVT) and PE in adults