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Nov 20, 2012 · Bayer HealthCare’s oral anticoagulant Xarelto ® (rivaroxaban) has been approved by the European Commission (EC) for the treatment of pulmonary embolism (PE) and the prevention of recurrent deep vein thrombosis (DVT) and PE in adults This approval makes rivaroxaban the only novel oral anticoagulant approved in this indication in the EU Mar 22, 2013 · The European Committee for Medicinal Products for Human Use (CHMP) has recommended approval of Bayer HealthCare’s oral anticoagulant Xarelto ® (rivaroxaban) 2 5mg twice-daily in combination with standard antiplatelet therapy for the prevention of atherothrombotic events (myocardial infarction, cardiovascular death or stroke) after an Acute Coronary Syndrome (ACS) in adult patients with XARELTO 2 5 mg Film-coated tablet Ref [7073] Active ingredients: Rivaroxaban Source: European Medicines Agency (EU) Revision Year: 2024 Publisher: Bayer AG, 51368 Leverkusen, Germany 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 - Rivaroxaban registered and approved in Europe on PharmaCompass com European Medicines Agency – Xarelto ® Product Information Xarelto Product Information in all official languages of the European Union provided by the European Medicines Agency Xarelto com portal Report a side effect Prescribing information ©2022 Bayer AG This website contains information on Xarelto (rivaroxaban) which is based on the Summary of Product Characteristics (SPC) as approved by the European Commission It is intended to provide information to an international audience outside the USA and UK
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