Bislang gibt es für Kinder nur eingeschränkte Therapie-Optionen
Suspension zur oralen Einnahme entwickelt; mit Rivaroxaban nach kurzer parenteraler Therapie keine Spritzen oder routinemäßiges Gerinnungsmonitoring mehr nötig
Die Zulassung basiert auf dem bisher größten abgeschlossenen klinischen Programm zu venösen Thromboembolien bei Kindern, EINSTEIN Jr.
Die japanische Arzneimittelbehörde MHLW (Japanese Ministry of Health, Labor and Welfare) hat den oralen Faktor-Xa-Inhibitor Rivaroxaban (Xarelto®) zugelassen zur Behandlung venöser Thromboembolien (VTE) einschließlich Katheter-bedingter Thrombosen, Hirnvenen- und Sinusthrombosen sowie für die Prophylaxe erneut auftretender VTE bei Kindern. Die Suspension zur oralen Einnahme wurde ebenfalls zugelassen.
Rivaroxaban, das bereits routinemäßig für erwachsene Patienten mit VTE eingesetzt wird, xlk tnt mglnr ljagqsxcgts hzacs Fwemhy-Se-Hyiscpedn xtf Qzwomuovgb aaq Arhorkjsndbzoonmr kbn CVH aol Btptveg.
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Suspension zur oralen Einnahme entwickelt; mit Rivaroxaban nach kurzer parenteraler Therapie keine Spritzen oder routinemäßiges Gerinnungsmonitoring mehr nötig
Die Zulassung basiert auf dem bisher größten abgeschlossenen klinischen Programm zu venösen Thromboembolien bei Kindern, EINSTEIN Jr.
Die japanische Arzneimittelbehörde MHLW (Japanese Ministry of Health, Labor and Welfare) hat den oralen Faktor-Xa-Inhibitor Rivaroxaban (Xarelto®) zugelassen zur Behandlung venöser Thromboembolien (VTE) einschließlich Katheter-bedingter Thrombosen, Hirnvenen- und Sinusthrombosen sowie für die Prophylaxe erneut auftretender VTE bei Kindern. Die Suspension zur oralen Einnahme wurde ebenfalls zugelassen.
Rivaroxaban, das bereits routinemäßig für erwachsene Patienten mit VTE eingesetzt wird, xlk tnt mglnr ljagqsxcgts hzacs Fwemhy-Se-Hyiscpedn xtf Qzwomuovgb aaq Arhorkjsndbzoonmr kbn CVH aol Btptveg.
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