Nebenwirkungen · Ituxredi
Ituxredi 100 mg concentrate for solution for infusion Ituxredi 500 mg concentrate for solution for infusion · Abschnitt 4.8 · PDF-Seite 28
HOS-152183 · Präparat HOS-100701
In GPA/MPA Study 2 (adult maintenance study), 7/57 (12%) patients in the rituximab arm experienced at least one infusion-related reaction. The incidence of IRR symptoms was highest during or after the first infusion (9%) and decreased with subsequent infusions (< 4%). All IRR symptoms were mild or moderate and most of them were reported from the SOCs Respiratory, Thoracic and Mediastinal Disorders and Skin and Subcutaneous Tissue disorders.
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Version 2025-07-09T10:02:28Z · SHA-256 65f947c73c59460b3d1812ff80010d6719d500cc410ebccf88cf20b48b9c9fe9 · Passage 9ad0e04e8c2a439af74181595dab34013b3d90e0fcea5fc60cf4c3a71fa98777 · Zeichen 46647–47091 im Abschnitt