Nebenwirkungen · Tevimbra
Tevimbra 100 mg concentrate for solution for infusion · Abschnitt 4.8 · PDF-Seite 11
HOS-150208 · Präparat HOS-100272
The safety of tislelizumab given in combination with chemotherapy is based on data in 1950 patients across multiple tumour types who received 200 mg tislelizumab every 3 weeks, with the exception of study BGB A317-315 where patients also received tislelizumab at a dose of 400 mg once every 6 weeks as adjuvant treatment after neoadjuvant therapy and surgery. The most common adverse
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Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
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