Kesatuan Eropah - Sweden - EMA (European Medicines Agency)

hansa biopharma ab - imlifidase - desensitization, immunologic; kidney transplantation - immunsuppressiva - idefirix is indicated for desensitisation treatment of highly sensitised adult kidney transplant patients with positive crossmatch against an available deceased donor. the use of idefirix should be reserved for patients unlikely to be transplanted under the available kidney allocation system including prioritisation programmes for highly sensitised patients.

Kesatuan Eropah - Sweden - EMA (European Medicines Agency)

beigene ireland ltd - zanubrutinib - waldenstrom macroglobulinemia - antineoplastiska medel - brukinsa as monotherapy is indicated for the treatment of adult patients with waldenström’s macroglobulinaemia (wm) who have received at least one prior therapy, or in first line treatment for patients unsuitable for chemo-immunotherapy. brukinsa as monotherapy is indicated for the treatment of adult patients with marginal zone lymphoma (mzl) who have received at least one prior anti-cd20-based therapy. brukinsa as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukemia (cll).

Kesatuan Eropah - Sweden - EMA (European Medicines Agency)

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%.

Kesatuan Eropah - Sweden - EMA (European Medicines Agency)

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

Sweden - Sweden - Läkemedelsverket (Medical Products Agency)

omrix biopharmaceuticals sa - anti-hepatit b-immunglobulin, humant - infusionsvätska, lösning - 50 ie/ml - anti-hepatit b-immunglobulin, humant 50 ie aktiv substans - immunglobulin mot hepatit b

Sweden - Sweden - Läkemedelsverket (Medical Products Agency)

omrix biopharmaceuticals sa - kalciumkloriddihydrat; koagulerbart protein, humant; tranexamsyra; trombin, humant - lösningar till vävnadslim - kalciumkloriddihydrat 5,6 - 6,2 mg aktiv substans; tranexamsyra 85 - 105 mg aktiv substans; mannitol hjälpämne; trombin, humant 800 - 1200 ie aktiv substans; koagulerbart protein, humant 40 - 60 mg aktiv substans - humant

Sweden - Sweden - Läkemedelsverket (Medical Products Agency)

omrix biopharmaceuticals n.v. - lösningar till vävnadslim

Sweden - Sweden - Läkemedelsverket (Medical Products Agency)

omrix biopharmaceuticals n.v. - matrix till vävnadslim

Kesatuan Eropah - Sweden - EMA (European Medicines Agency)

sanofi b.v. - klofarabin - prekursorcell lymfoblastisk leukemi-lymfom - antineoplastiska medel - behandling av akut lymfatisk leukemi (all) hos pediatriska patienter som har recidiverat eller är refraktärt efter att ha fått minst två tidigare behandlingar och där finns det ingen annan behandlingsalternativ förväntas resultera i en varaktig respons. säkerhet och effekt har utvärderats i studier av patienter ≤ 21 år vid första diagnosen.

Kesatuan Eropah - Sweden - EMA (European Medicines Agency)

sanofi winthrop industrie - insulin glargin, lixisenatide - diabetes mellitus, typ 2 - läkemedel som används vid diabetes - suliqua is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus to improve glycaemic control as an adjunct to diet and exercise in addition to metformin with or without sglt-2 inhibitors.