Sveitsi - italia - Swissmedic (Swiss Agency for Therapeutic Products)

bristol-myers squibb sa - daclatasvirum - filmtabletten - tablet: daclatasvirum 30 mg ut daclatasviri dihydrochloridum, colore.: e 132, excipiens pro compresso obducto. - chronische epatite c - synthetika

Sveitsi - italia - Swissmedic (Swiss Agency for Therapeutic Products)

bristol-myers squibb sa - daclatasvirum - filmtabletten - daclatasvirum 60 mg ut daclatasviri dihydrochloridum, colore.: e 132, excipiens pro compresso obducto. - chronische epatite c - synthetika

Sveitsi - italia - Swissmedic (Swiss Agency for Therapeutic Products)

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

Sveitsi - italia - Swissmedic (Swiss Agency for Therapeutic Products)

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

Sveitsi - italia - Swissmedic (Swiss Agency for Therapeutic Products)

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

Sveitsi - italia - Swissmedic (Swiss Agency for Therapeutic Products)

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

Sveitsi - italia - Swissmedic (Swiss Agency for Therapeutic Products)

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

Euroopan unioni - italia - EMA (European Medicines Agency)

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.

Euroopan unioni - italia - EMA (European Medicines Agency)

bristol myers squibb pharma eeig - luspatercept - anemia; myelodysplastic syndromes; beta-thalassemia - altre antianemico preparazioni - reblozyl is indicated for the treatment of adult patients with transfusion-dependent anaemia due to very low, low and intermediate-risk myelodysplastic syndromes (mds) with ring sideroblasts, who had an unsatisfactory response to or are ineligible for erythropoietin-based therapy (see section 5. reblozyl is indicated in adults for the treatment of anaemia associated with transfusion dependent and non transfusion dependent beta thalassaemia (see section 5.

Euroopan unioni - italia - EMA (European Medicines Agency)

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.