Vipdomet Evrópusambandið - danska - EMA (European Medicines Agency)

vipdomet

takeda pharma a/s - alogliptin benzoat, metformin-hydrochlorid - diabetes mellitus, type 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - vipdomet is indicated in the treatment of adult patients aged 18 years and older with type-2 diabetes mellitus:as an adjunct to diet and exercise to improve glycaemic control in adult patients, inadequately controlled on their maximal tolerated dose of metformin alone, or those already being treated with the combination of alogliptin and metformin;in combination with pioglitazone (i. triple combination therapy) as an adjunct to diet and exercise in adult patients inadequately controlled on their maximal tolerated dose of metformin and pioglitazone;in combination with insulin (i. triple kombinationsbehandling) som supplement til diæt og motion til forbedring af glykæmisk kontrol hos patienter, når insulin på en stabil dosis og metformin alene ikke giver tilstrækkelig glykæmisk kontrol.

Fintepla Evrópusambandið - danska - EMA (European Medicines Agency)

fintepla

ucb pharma s.a.   - fenfluramine hydrochloride - epilepsies, myoclonic - antiepileptika, - treatment of seizures associated with dravet syndrome as an add-on therapy to other antiepileptic medicines for patients 2 years of age and older. fintepla is indicated for the treatment of seizures associated with dravet syndrome and lennox-gastaut syndrome as an add-on therapy to other anti-epileptic medicines for patients 2 years of age and older.

Adtralza Evrópusambandið - danska - EMA (European Medicines Agency)

adtralza

leo pharma a/s - tralokinumab - dermatitis, atopisk - andre dermatologiske præparater - adtralza is indicated for the treatment of moderate to severe atopic dermatitis in adult and adolescent patients 12 years and older who are candidates for systemic therapy.

Edevira 0,5 mg filmovertrukne tabletter Danmörk - danska - Lægemiddelstyrelsen (Danish Medicines Agency)

edevira 0,5 mg filmovertrukne tabletter

pharmathen s.a. - entecavir (monohydrat) - filmovertrukne tabletter - 0,5 mg

Edevira 1 mg filmovertrukne tabletter Danmörk - danska - Lægemiddelstyrelsen (Danish Medicines Agency)

edevira 1 mg filmovertrukne tabletter

pharmathen s.a. - entecavir (monohydrat) - filmovertrukne tabletter - 1 mg

Seretide 50+250 mikrog./dosis inhalationspulver, afdelt Danmörk - danska - Lægemiddelstyrelsen (Danish Medicines Agency)

seretide 50+250 mikrog./dosis inhalationspulver, afdelt

glaxosmithkline pharma a/s - fluticasonpropionat, salmeterolxinafoat - inhalationspulver, afdelt - 50+250 mikrog./dosis

Yescarta Evrópusambandið - danska - EMA (European Medicines Agency)

yescarta

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.

Onureg Evrópusambandið - danska - 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).

Firmagon Evrópusambandið - danska - EMA (European Medicines Agency)

firmagon

ferring pharmaceuticals a/s - degarelix - prostatiske neoplasmer - endokrine terapi - firmagon is a gonadotrophin releasing hormone (gnrh) antagonist indicated:- for treatment of adult male patients with advanced hormone-dependent prostate cancer. - for treatment of high-risk localised and locally advanced hormone dependent prostate cancer in combination with radiotherapy. - as neo-adjuvant treatment prior to radiotherapy in patients with high-risk localised or locally advanced hormone dependent prostate cancer.

Lysodren Evrópusambandið - danska - EMA (European Medicines Agency)

lysodren

hra pharma rare diseases - mitotane - binyrebark-neoplasmer - antineoplastiske midler - symptomatisk behandling af avanceret (uopløselig, metastatisk eller tilbagefaldende) binyrebarkalsk carcinom. effekten af lysodren på ikke-funktionelle binyrebarkhormoner karcinom er ikke etableret.