Nebenwirkungen · Riximyo
Riximyo 100 mg concentrate for solution for infusion Riximyo 500 mg concentrate for solution for infusion · Abschnitt 4.8 · PDF-Seite 25
HOS-141066 · Präparat HOS-098602
In a trial designed to evaluate the safety of a more rapid rituximab infusion in patients with rheumatoid arthritis, patients with moderate-to-severe active RA who did not experience a serious IRR during or within 24 hours of their first studied infusion were allowed to receive a 2-hour intravenous infusion of rituximab. Patients with a history of a serious infusion reaction to a biologic therapy for RA were excluded from entry. The incidence, types and severity of IRRs were consistent with that observed historically. No serious IRRs were observed.
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Version 2026-09-04T16:41:00Z · SHA-256 4fe21e50fef50537643123868d3f044762b7d55eab7d50a56c1d469305291ee4 · Passage d02bb29ca19fca2d8f4f8f460c4a177890a9902163da23f1cdba5486494076a8 · Zeichen 36145–36699 im Abschnitt