European Union - Swedish - EMA (European Medicines Agency)

eli lilly nederland b.v. - insulin lispro - diabetes mellitus - läkemedel som används vid diabetes - behandling av diabetes mellitus hos vuxna, ungdomar och barn i åldern 1 år och äldre. behandling av diabetes mellitus hos vuxna.

Sweden - Swedish - Läkemedelsverket (Medical Products Agency)

radiopharmacy laboratory ltd. - exametazim - beredningssats för radioaktivt läkemedel - 0,5 mg - exametazim 0,5 mg aktiv substans

European Union - Swedish - 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.

Sweden - Swedish - Läkemedelsverket (Medical Products Agency)

interchemie werken de adelaar eesti as - ketoprofen - injektionsvätska, lösning - 100 mg/ml - bensylalkohol hjälpämne; ketoprofen 100 mg aktiv substans - häst, nöt, svin

European Union - Swedish - EMA (European Medicines Agency)

laboratoire francais du fractionnement et des biotechnologies - eptacog beta (activated) - hemophilia a; hemophilia b - hemostatika - cevenfacta is indicated in adults and adolescents (12 years of age and older) for the treatment of bleeding episodes and for the prevention of bleeding in those undergoing surgery or invasive procedures in the following patient groups:in patients with congenital haemophilia with high-responding inhibitors to coagulation factors viii or ix (i. ≥5 bethesda units (bu)); in patients with congenital haemophilia with low titre inhibitors (bu.

Sweden - Swedish - Läkemedelsverket (Medical Products Agency)

stada arzneimittel ag - rivaroxaban - filmdragerad tablett - 2,5 mg - rivaroxaban 2,5 mg aktiv substans; natriumlaurilsulfat hjälpämne; laktosmonohydrat hjälpämne

European Union - Swedish - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - teriparatid - osteoporosis; osteoporosis, postmenopausal - calciumhomeostas - teriparatide sun is indicated in adults. treatment of osteoporosis in postmenopausal women and in men at increased risk of fracture (see section 5. in postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures has been demonstrated. treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at increased risk for fracture (see section 5.

Sweden - Swedish - Läkemedelsverket (Medical Products Agency)

orion corporation - rivaroxaban - filmdragerad tablett - 2,5 mg - natriumlaurilsulfat hjälpämne; laktosmonohydrat hjälpämne; rivaroxaban 2,5 mg aktiv substans

Sweden - Swedish - Läkemedelsverket (Medical Products Agency)

cis bio international - albumin, humant - beredningssats för radioaktivt läkemedel - 10 mg - albumin, humant 10 mg aktiv substans - humant

Sweden - Swedish - Läkemedelsverket (Medical Products Agency)

astellas pharma gmbh - bendamustinhydroklorid - pulver till koncentrat till infusionsvätska, lösning - 2,5 mg/ml - mannitol hjälpämne; bendamustinhydroklorid 2,5 mg aktiv substans - bendamustin