Vidaza Kesatuan Eropah - Denmark - EMA (European Medicines Agency)

vidaza

bristol-myers squibb pharma eeig - azacitidin - myelodysplastic syndromes; leukemia, myelomonocytic, chronic; leukemia, myeloid, acute - antineoplastiske midler - vidaza is indicated for the treatment of adult patients who are not eligible for haematopoietic stem cell transplantation (hsct) with: intermediate 2 and high-risk myelodysplastic syndromes (mds) according to the international prognostic scoring system (ipss),chronic myelomonocytic leukaemia (cmml) with 10 29 % marrow blasts without myeloproliferative disorder,acute myeloid leukaemia (aml) with 20 30 % blasts and multi-lineage dysplasia, according to world health organisation (who) classification. vidaza is indicated for the treatment of adult patients aged 65 years or older who are not eligible for hsct with aml with >30% marrow blasts according to the who classification.

Kenalog 40 mg/ml injektionsvæske, suspension Denmark - Denmark - Lægemiddelstyrelsen (Danish Medicines Agency)

kenalog 40 mg/ml injektionsvæske, suspension

bristol-myers squibb ab - triamcinolonacetonid - injektionsvæske, suspension - 40 mg/ml

Pentrexyl 1 g pulver til injektions-/infusionsvæske, opløsning Denmark - Denmark - Lægemiddelstyrelsen (Danish Medicines Agency)

pentrexyl 1 g pulver til injektions-/infusionsvæske, opløsning

bristol-myers squibb ab - ampicillinnatrium - pulver til injektions-/infusionsvæske, opløsning - 1 g

Pentrexyl 2 g pulver til injektions-/infusionsvæske, opløsning Denmark - Denmark - Lægemiddelstyrelsen (Danish Medicines Agency)

pentrexyl 2 g pulver til injektions-/infusionsvæske, opløsning

bristol-myers squibb ab - ampicillinnatrium - pulver til injektions-/infusionsvæske, opløsning - 2 g

Pentrexyl 500 mg pulver til injektions-/infusionsvæske, opløsning Denmark - Denmark - Lægemiddelstyrelsen (Danish Medicines Agency)

pentrexyl 500 mg pulver til injektions-/infusionsvæske, opløsning

bristol-myers squibb ab - ampicillinnatrium - pulver til injektions-/infusionsvæske, opløsning - 500 mg

Zeposia Kesatuan Eropah - Denmark - EMA (European Medicines Agency)

zeposia

bristol-myers squibb pharma eeig - ozanimod hydrochlorid - multiple sclerosis, relapsing-remitting; colitis, ulcerative - immunosuppressiva - 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.

Reblozyl Kesatuan Eropah - Denmark - EMA (European Medicines Agency)

reblozyl

bristol myers squibb pharma eeig - luspatercept - anemia; myelodysplastic syndromes; beta-thalassemia - andre præparater antianemic - 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.

Onureg Kesatuan Eropah - Denmark - EMA (European Medicines Agency)

onureg

bristol-myers squibb pharma eeig - azacitidin - leukæmi, myeloid, akut - antineoplastiske midler - 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).

Opdualag Kesatuan Eropah - Denmark - EMA (European Medicines Agency)

opdualag

bristol-myers squibb pharma eeig - nivolumab, relatlimab - melanom - 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%.