Nebenwirkungen · Ituxredi
Ituxredi 100 mg concentrate for solution for infusion Ituxredi 500 mg concentrate for solution for infusion · Abschnitt 4.8 · PDF-Seite 27
HOS-152176 · Präparat HOS-100701
The overall safety profile was consistent with the well-established safety profile for rituximab in approved autoimmune indications, including GPA/MPA. Overall, 4% of patients in the rituximab arm experienced adverse events leading to discontinuation. Most adverse events in the rituximab arm were mild or moderate in intensity. No patients in the rituximab arm had fatal adverse events.
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Version 2025-07-09T10:02:28Z · SHA-256 65f947c73c59460b3d1812ff80010d6719d500cc410ebccf88cf20b48b9c9fe9 · Passage 3e64fb5ee3ca6d8ca1d74acb343a0234253dea862e5d75eff0b692fe396313b8 · Zeichen 43728–44121 im Abschnitt