সুইডেন - সুইডিশ - Läkemedelsverket (Medical Products Agency)

bristol-myers squibb ab - didanosin - enterokapsel, hård - 125 mg - didanosin 125 mg aktiv substans; natriumlaurilsulfat hjälpämne - didanosin

সুইডেন - সুইডিশ - Läkemedelsverket (Medical Products Agency)

bristol-myers squibb ab - didanosin - enterokapsel, hård - 200 mg - didanosin 200 mg aktiv substans; natriumlaurilsulfat hjälpämne - didanosin

সুইডেন - সুইডিশ - Läkemedelsverket (Medical Products Agency)

bristol-myers squibb ab - didanosin - enterokapsel, hård - 250 mg - didanosin 250 mg aktiv substans; propylenglykol hjälpämne; natriumlaurilsulfat hjälpämne - didanosin

সুইডেন - সুইডিশ - Läkemedelsverket (Medical Products Agency)

bristol-myers squibb ab - didanosin - enterokapsel, hård - 400 mg - natriumlaurilsulfat hjälpämne; didanosin 400 mg aktiv substans; propylenglykol hjälpämne - didanosin

সুইডেন - সুইডিশ - Läkemedelsverket (Medical Products Agency)

bristol-myers squibb ab - nystatin - oral suspension - 100000 iu/ml - nystatin 100000 ie aktiv substans; metylparahydroxibensoat hjälpämne; xylitol hjälpämne - nystatin

সুইডেন - সুইডিশ - Läkemedelsverket (Medical Products Agency)

bristol-myers squibb ab - adenosin; allopurinol; glutation; hydroxietylstärkelse, 250/0.45; kaliumdivätefosfat; kaliumhydroxid; laktobionsyra; magnesiumsulfatheptahydrat; natriumhydroxid; raffinospentahydrat - vätska för organförvaring - hydroxietylstärkelse, 250/0.45 50 mg aktiv substans; adenosin 1,34 mg aktiv substans; allopurinol 136 mikrog aktiv substans; glutation 922 mikrog aktiv substans; raffinospentahydrat 17,83 mg aktiv substans; magnesiumsulfatheptahydrat 1,23 mg aktiv substans; kaliumdivätefosfat 3,4 mg aktiv substans; kaliumhydroxid 5,611 mg aktiv substans; natriumhydroxid 1,08 mg aktiv substans; laktobionsyra 35,83 mg aktiv substans - spädningsvätskor och spolvätskor

ইউরোপীয় ইউনিয়ন - সুইডিশ - EMA (European Medicines Agency)

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

ইউরোপীয় ইউনিয়ন - সুইডিশ - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - azacitidin - leukemi, myeloid, akut - antineoplastiska medel - 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).

ইউরোপীয় ইউনিয়ন - সুইডিশ - 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 - antineoplastiska medel - 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.

ইউরোপীয় ইউনিয়ন - সুইডিশ - 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 - antineoplastiska medel - 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.