Rivaroxaban in der vaskulären Dosierung (zweimal täglich 2,5 mg plus Acetylsalicylsäure 100 mg einmal täglich) führte zu einer Verminderung des kombinierten Risikos für Schlaganfälle, Herzinfarkte und kardiovaskuläre Todesfälle um 24 %(1) / Der Zulassungsantrag basiert auf der klinischen Studie COMPASS / Nach Zulassung wird Rivaroxaban in der vaskulären Dosierung zusammen mit Acetylsalicylsäure der einzige nicht-Vitamin-K-basierte orale Gerinnungshemmer (NOAK) für diese Patientengruppe sein
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