Európska únia - francúzština - EMA (European Medicines Agency)

bristol myers squibb pharma eeig - luspatercept - anemia; myelodysplastic syndromes; beta-thalassemia - d'autres antianémique préparations - 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.

Európska únia - francúzština - EMA (European Medicines Agency)

bristol myers squibb pharma eeig - fedratinib dihydrochloride monohydrate - myeloproliferative disorders; primary myelofibrosis - agents antinéoplasiques - 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.

Európska únia - francúzština - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - azacitidine - leucémie, myéloïde, aiguë - agents antinéoplasiques - 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).

Európska únia - francúzština - EMA (European Medicines Agency)

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 - agents antinéoplasiques - 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.

Európska únia - francúzština - EMA (European Medicines Agency)

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 - agents antinéoplasiques - 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.

Európska únia - francúzština - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - nivolumab, relatlimab - mélanome - antineoplastic agents, monoclonal antibodies - opdualag is indicated for the first line treatment of advanced (unresectable or metastatic) melanoma in adults and adolescents 12 years of age and older with tumour cell pd l1 expression < 1%.

Európska únia - francúzština - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - deucravacitinib - psoriasis - immunosuppresseurs - treatment of moderate-to-severe plaque psoriasis in adults.

Európska únia - francúzština - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - mavacamten - cardiomyopathy, hypertrophic - autres préparations cardiaques - treatment of symptomatic obstructive hypertrophic cardiomyopathy.

Európska únia - francúzština - EMA (European Medicines Agency)

bristol-myers squibb / pfizer eeig - associés à l'apixaban - arthroplasty; venous thromboembolism - agents antithrombotiques - pour eliquis 2. 5 mg, comprimés pelliculés:prévention de la thromboembolie veineuse (tev) chez les patients adultes qui ont subi élective de la hanche ou du genou. prévention des avc et des embolies systémiques chez des patients adultes atteints de fa non valvulaire (nvaf), avec un ou plusieurs facteurs de risque, comme les antécédents d'avc ou d'accident ischémique transitoire (tia); âge ≥ 75 ans; hypertension artérielle; diabète; insuffisance cardiaque symptomatique (classe nyha ≥ ii). le traitement de la thrombose veineuse profonde (tvp) et l'embolie pulmonaire (ep) et prévention des récidives de tvp et l'ep chez les adultes (voir la section 4. 4 pour en présentant des répercussions hémodynamiques instables pe malades). pour eliquis 5 mg, comprimés pelliculés:prévention des avc et des embolies systémiques chez des patients adultes atteints de fa non valvulaire (nvaf), avec un ou plusieurs facteurs de risque, comme les antécédents d'avc ou d'accident ischémique transitoire (tia); âge≥ 75 ans; hypertension artérielle; diabète; insuffisance cardiaque symptomatique (classe nyha ≥ ii). le traitement de la thrombose veineuse profonde (tvp) et l'embolie pulmonaire (ep) et prévention des récidives de tvp et l'ep chez les adultes (voir la section 4. 4 pour en présentant des répercussions hémodynamiques instables pe malades).

Kanada - francúzština - Health Canada

bristol-myers squibb canada - apixaban - comprimé - 2.5mg - apixaban 2.5mg - direct factor xa inhibitors