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Xarelto® Indications __________ The 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 XARELTO 20 mg Film-coated tablet Ref [7444] Active ingredients: Rivaroxaban Source: European Medicines Agency (EU) Revision Year: 2024 Publisher: Bayer AG, 51368 Leverkusen, GermanyOct 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 XARELTO 20 mg Film-coated tablet Ref [7444] Active ingredients: Rivaroxaban Source: European Medicines Agency (EU) Revision Year: 2024 Publisher: Bayer AG, 51368 Leverkusen, GermanyThis 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 Nov 20, 2012 · The European approval follows clearance from the US FDA earlier this month for Xarelto’s use in the treatment of DVT or PE, as well as to reduce the risk of recurrent DVT and PE following initial treatment