The objective of this study is to evaluate the efficacy, safety, pharmacokinetics (PK) and pharmacodynamics (PD) of rivaroxaban in the treatment of pulmonary embolism (PE) and the prevention of the occurrence and the recurrence of deep vein thrombosis (DVT) or PE in Japanese patients with acute symptomatic PE with or without symptomatic DVT.
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Number of participants with newly onset of symptomatic venous thromboembolism (VTE)
Timeframe: Up to 12 months
Number of clinically relevant bleedings
Timeframe: Up to 2 days after last dose