Opdivo 40 mg/4 ml Concentrato per soluzione per Infusione שווייץ - איטלקית - Swissmedic (Swiss Agency for Therapeutic Products)

opdivo 40 mg/4 ml concentrato per soluzione per infusione

bristol-myers squibb sa - nivolumabum - concentrato per soluzione per infusione - nivolumabum 40 mg, natrii citras dihydricus, natrii chloridum, mannitolum, acidum penteticum, polysorbatum 80, acidum hydrochloridum, natrii hydroxidum, aqua ad iniectabile q.s. ad solutionem pro 4 ml corresp. natrium 10 mg. - onkologikum - biotechnologika

Opdivo 100 mg/10 ml Concentrato per soluzione per Infusione שווייץ - איטלקית - Swissmedic (Swiss Agency for Therapeutic Products)

opdivo 100 mg/10 ml concentrato per soluzione per infusione

bristol-myers squibb sa - nivolumabum - concentrato per soluzione per infusione - nivolumabum 100 mg, natrii citras dihydricus, natrii chloridum, mannitolum, acidum penteticum, polysorbatum 80, acidum hydrochloridum, natrii hydroxidum, aqua ad iniectabile q.s. ad solutionem pro 10 ml corresp. natrium 25 mg. - onkologikum - biotechnologika

Empliciti 300 mg Polvere per soluzione per Infusione שווייץ - איטלקית - Swissmedic (Swiss Agency for Therapeutic Products)

empliciti 300 mg polvere per soluzione per infusione

bristol-myers squibb sa - elotuzumabum - polvere per soluzione per infusione - elotuzumabum 300 mg, natrii citras dihydricus corrisp. sodio 3.9 mg, acido citricum monohydricum, zucchero, polysorbatum 80 per il vetro. - multipli myelom - biotechnologika

Empliciti 400 mg Polvere per soluzione per Infusione שווייץ - איטלקית - Swissmedic (Swiss Agency for Therapeutic Products)

empliciti 400 mg polvere per soluzione per infusione

bristol-myers squibb sa - elotuzumabum - polvere per soluzione per infusione - elotuzumabum 400 mg, natrii citras dihydricus corrisp. sodio 5.3 mg, acido citricum monohydricum, zucchero, polysorbatum 80 per il vetro. - multipli myelom - biotechnologika

Opdivo 240 mg/24 ml Concentrato per soluzione per Infusione שווייץ - איטלקית - Swissmedic (Swiss Agency for Therapeutic Products)

opdivo 240 mg/24 ml concentrato per soluzione per infusione

bristol-myers squibb sa - nivolumabum - concentrato per soluzione per infusione - nivolumabum 240 mg, natrii citras dihydricus, natrii chloridum, mannitolum, acidum penteticum, polysorbatum 80, acidum hydrochloridum, natrii hydroxidum, aqua ad iniectabile q.s. ad solutionem pro 24 ml corresp. natrium 60 mg. - onkologikum - biotechnologika

Zeposia האיחוד האירופי - איטלקית - EMA (European Medicines Agency)

zeposia

bristol-myers squibb pharma eeig - ozanimod hydrochloride - multiple sclerosis, relapsing-remitting; colitis, ulcerative - immunosoppressori - multiple sclerosiszeposia is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis (rrms) with active disease as defined by clinical or imaging features. ulcerative colitiszeposia is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis (uc) who have had an inadequate response, lost response, or were intolerant to either conventional therapy or a biologic agent.

Inrebic האיחוד האירופי - איטלקית - EMA (European Medicines Agency)

inrebic

bristol myers squibb pharma eeig - fedratinib dihydrochloride monohydrate - myeloproliferative disorders; primary myelofibrosis - agenti antineoplastici - inrebic is indicated for the treatment of disease-related splenomegaly or symptoms in adult patients with primary myelofibrosis, post polycythaemia vera myelofibrosis or post essential thrombocythaemia myelofibrosis who are janus associated kinase (jak) inhibitor naïve or have been treated with ruxolitinib.

Onureg האיחוד האירופי - איטלקית - EMA (European Medicines Agency)

onureg

bristol-myers squibb pharma eeig - azacitidina - leucemia, mieloide, acuta - agenti antineoplastici - onureg is indicated as maintenance therapy in adult patients with acute myeloid leukaemia (aml) who achieved complete remission (cr) or complete remission with incomplete blood count recovery (cri) following induction therapy with or without consolidation treatment and who are not candidates for, including those who choose not to proceed to, hematopoietic stem cell transplantation (hsct).

Abecma האיחוד האירופי - איטלקית - EMA (European Medicines Agency)

abecma

bristol-myers squibb pharma eeig - idecabtagene vicleucel - multiple myeloma; neoplasms; cancer; neoplasms, plasma cell; hemostatic disorders; vascular diseases; cardiovascular diseases; paraproteinemias; blood protein disorders; hematologic diseases; hemic and lymphatic diseases; hemorrhagic disorders; infectious mononucleosis; lymphoproliferative disorders; immunoproliferative disorders; immune system diseases - agenti antineoplastici - abecma is indicated for the treatment of adult patients with relapsed and refractory multiple myeloma who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor and an anti cd38 antibody and have demonstrated disease progression on the last therapy.

Breyanzi האיחוד האירופי - איטלקית - EMA (European Medicines Agency)

breyanzi

bristol-myers squibb pharma eeig - cd19-directed genetically modified autologous cell-based product consisting of purified cd8+ t-cells (cd8+ cells), cd19-directed genetically modified autologous cell-based product consisting of purified cd4+ t cells (cd4+ cells) - lymphoma, large b-cell, diffuse; lymphoma, follicular; mediastinal neoplasms - agenti antineoplastici - breyanzi is indicated for the treatment of adult patients with diffuse large b-cell lymphoma (dlbcl), high grade b-cell lymphoma (hgbcl), primary mediastinal large b-cell lymphoma (pmbcl) and follicular lymphoma grade 3b (fl3b), who relapsed within 12 months from completion of, or are refractory to, first-line chemoimmunotherapy.