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Xarelto®(rivaroxaban) – New indications, new formulation approval

On December 20, 2021, the FDA approved Janssen’s Xarelto (rivaroxaban), for

  • Treatment of venous thromboembolism (VTE) and the reduction in the risk of recurrent VTE in pediatric patients from birth to less than 18 years after at least 5 days of initial parenteral anticoagulant treatment; and
  • Thromboprophylaxis in pediatric patients aged 2 years and older with congenital heart disease who have undergone the Fontan procedure

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