Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

norgine b.v. - ascorbinsyre, kaliumchlorid, macrogol 3350, natriumascorbat, natriumchlorid, natriumsulfat, vandfrit - pulver til oral opløsning

Den Europæiske Union - dansk - EMA (European Medicines Agency)

alnylam netherlands b.v. - patisiran natrium - amyloidose, familiær - andre narkotika stoffer - onpattro er indiceret til behandling af arvelige transthyretin-medieret amyloidose (hattr amyloidose) hos voksne patienter med fase 1 eller fase 2 polyneuropati.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

kite pharma eu b.v. - axicabtagene ciloleucel - lymphoma, follicular; lymphoma, large b-cell, diffuse - antineoplastiske midler - yescarta is indicated for the treatment of adult patients with diffuse large b cell lymphoma (dlbcl) and high-grade b-cell lymphoma (hgbl) that relapses within 12 months from completion of, or is refractory to, first-line chemoimmunotherapy. yescarta is indicated for the treatment of adult patients with relapsed or refractory (r/r) dlbcl and primary mediastinal large b cell lymphoma (pmbcl), after two or more lines of systemic therapy. yescarta is indicated for the treatment of adult patients with r/r follicular lymphoma (fl) after three or more lines of systemic therapy.

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

paranova danmark a/s - betula verrucosa ehrh. (vortebirk, synonym af b. pendula roth) - injektionsvæske, suspension - 100.000 sq-u/ml

Den Europæiske Union - dansk - EMA (European Medicines Agency)

sanofi winthrop industrie - isatuximab - multipelt myelom - antineoplastiske midler - sarclisa is indicated: in combination with pomalidomide and dexamethasone, for the treatment of adult patients with relapsed and refractory multiple myeloma (mm) who have received at least two prior therapies including lenalidomide and a proteasome inhibitor (pi) and have demonstrated disease progression on the last therapy. in combination with carfilzomib and dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least one prior therapy (see section 5.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

stemline therapeutics b.v. - tagraxofusp - lymphoma - antineoplastiske midler - elzonris is indicated as monotherapy for the first-line treatment of adult patients with blastic plasmacytoid dendritic cell neoplasm (bpdcn).

Den Europæiske Union - dansk - EMA (European Medicines Agency)

sanofi b.v. - avalglucosidase alfa - glycogen opbevaring sygdom type ii - andre alimentary tract and metabolism produkter, - nexviadyme (avalglucosidase alfa) is indicated for long-term enzyme replacement therapy for the treatment of patients with pompe disease (acid α-glucosidase deficiency).

Den Europæiske Union - dansk - EMA (European Medicines Agency)

sanofi b.v. - sutimlimab - hemolysis; anemia, hemolytic, autoimmune - immunosuppressiva - enjaymo is indicated for the treatment of haemolytic anaemia in adult patients with cold agglutinin disease (cad).

Den Europæiske Union - dansk - EMA (European Medicines Agency)

takeda pharma a/s - azilsartan medoxomil - forhøjet blodtryk - agenter, der virker på renin-angiotensinsystemet - ipreziv er indiceret til behandling af essentiel hypertension hos voksne.