Nebenwirkungen · Polivy
Polivy 30 mg powder for concentrate for solution for infusion. Polivy 140 mg powder for concentrate for solution for infusion. · Abschnitt 4.8 · PDF-Seite 11
HOS-142653 · Präparat HOS-098846
In previously treated DLBCL patients treated with Polivy plus BR: The most frequently reported (≥ 30%) ADRs (all grades) in patients treated with Polivy plus BR in previously treated DLBCL were neutropenia (45.7%), diarrhoea (35.8%), nausea (33.1%), thrombocytopenia (32.5%), anaemia (31.8%) and neuropathy peripheral (30.5%). Serious adverse reactions were reported in 41.7% of Polivy plus BR treated patients. The most common serious adverse reactions reported in ≥ 5% of patients were: febrile neutropenia (10.6%), sepsis (9.9%), pneumonia (8.6%) and pyrexia (7.9%). The ADR leading to treatment regimen discontinuation in > 5% of patients treated with Polivy plus BR was thrombocytopenia (7.9%).
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Version 2026-10-20T16:17:00Z · SHA-256 a3e89d92646e20e619974ca0dc3eec49e6a7f37bd13a6556343aef72032c4fc0 · Passage 9a4145603f7a50d9b1b09027d70eb242eea26cf1e4d10f31d66fb13ed9850f34 · Zeichen 1861–2608 im Abschnitt