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Ituxredi
Eintrag öffnenItuxredi · 4.1 Therapeutic indications · 1
Eintrag öffnenItuxredi · 4.3 Contraindications · 1
Eintrag öffnenItuxredi · 4.3 · Active, severe infections (see section 4.4).
Eintrag öffnenItuxredi · 4.3 · Hypersensitivity to the active substance or to murine proteins, or to any of the excipients listed in section
Eintrag öffnenItuxredi · 4.3 · Patients in a severely immunocompromised state.
Eintrag öffnenItuxredi · 4.3 · Severe heart failure (New York Heart Association Class IV) or severe, uncontrolled cardiac disease for use in
Eintrag öffnenItuxredi · 4.4 Special warnings and precautions for use · 1
Eintrag öffnenItuxredi · 4.5 Interaction with other medicinal products and other forms of interaction · 1
Eintrag öffnenItuxredi · 4.5 · Co-administration with methotrexate had no effect on the pharmacokinetics of rituximab in rheumatoid arthritis
Eintrag öffnenItuxredi · 4.5 · Currently, there are limited data on possible drug interactions with rituximab.
Eintrag öffnenItuxredi · 4.5 · In CLL patients, co-administration with rituximab did not appear to have an effect on the pharmacokinetics of
Eintrag öffnenItuxredi · 4.5 · In patients with rheumatoid arthritis, 283 patients received subsequent therapy with a biologic DMARD followin
Eintrag öffnenItuxredi · 4.5 · Patients with human anti-mouse antibody (HAMA) or anti-drug antibody (ADA) titres may have allergic or hyperse
Eintrag öffnenItuxredi · 4.6 Fertility, pregnancy and lactation · 1
Eintrag öffnenItuxredi · 4.8 Undesirable effects · 1
Eintrag öffnenItuxredi · 4.8 · A multicentre, open-label randomised study of Lymphome Malin B chemotherapy (LMB) with or without rituximab wa
Eintrag öffnenItuxredi · 4.8 · A small number of spontaneous and literature cases of hypogammaglobulinaemia have been observed in paediatric
Eintrag öffnenItuxredi · 4.8 · A small number of spontaneous and literature cases of hypogammaglobulinaemia have been observed in paediatric
Eintrag öffnenItuxredi · 4.8 · A total of 309 paediatric patients received rituximab and were included in the safety analysis population. Pae
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