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

quviviq

idorsia pharmaceuticals deutschland gmbh - daridorexant hydrochloride - søvninitierings- og vedligeholdelsesforstyrrelser - psykoleptika - quviviq is indicated for the treatment of adult patients with insomnia characterised by symptoms present for at least 3 months and considerable impact on daytime functioning.

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

tepmetko

merck europe b.v. - tepotinib hydrochloride monohydrate - carcinom, ikke-småcellet lunge - antineoplastiske midler - tepmetko as monotherapy is indicated for the treatment of adult patients with advanced non-small cell lung cancer (nsclc) harbouring alterations leading to mesenchymal-epithelial transition factor gene exon 14 (metex14) skipping, who require systemic therapy following prior treatment with immunotherapy and/or platinum-based chemotherapy.

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

scemblix

novartis europharm limited - asciminib hydrochloride - leukæmi, myelogen, kronisk, bcr-abl positiv - antineoplastiske midler - scemblix is indicated for the treatment of adult patients with philadelphia chromosome positive chronic myeloid leukaemia in chronic phase (ph+ cml cp) previously treated with two or more tyrosine kinase inhibitors (see section 5.

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

pepaxti

oncopeptides ab - melphalan flufenamide hydrochloride - multipelt myelom - antineoplastiske midler - pepaxti is indicated, in combination with dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least three prior lines of therapies, whose disease is refractory to at least one proteasome inhibitor, one immunomodulatory agent, and one anti-cd38 monoclonal antibody, and who have demonstrated disease progression on or after the last therapy. for patients with a prior autologous stem cell transplantation, the time to progression should be at least 3 years from transplantation (see section 4.

Forvel 0,4 mg/ml injektions-/infusionsvæske, opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

forvel 0,4 mg/ml injektions-/infusionsvæske, opløsning

medochemie ltd. - naloxonhydrochlorid (vandfrit) - injektions-/infusionsvæske, opløsning - 0,4 mg/ml

Hytrin 2 mg tabletter Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

hytrin 2 mg tabletter

2care4 aps - terazosinhydrochlorid (vandfrit) - tabletter - 2 mg

Hytrin 2 mg tabletter Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

hytrin 2 mg tabletter

orifarm a/s - terazosinhydrochlorid (vandfrit) - tabletter - 2 mg

Hytrin 5 mg tabletter Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

hytrin 5 mg tabletter

orifarm a/s - terazosinhydrochlorid (vandfrit) - tabletter - 5 mg

Nexodal 0,4 mg/ml injektions-/infusionsvæske, opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

nexodal 0,4 mg/ml injektions-/infusionsvæske, opløsning

orpha devel handels- und vertr. - naloxonhydrochlorid (vandfrit) - injektions-/infusionsvæske, opløsning - 0,4 mg/ml

Prenoxad 0,9 mg/ml injektionsvæske, opløsning i fyldt injektionssprøjte Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

prenoxad 0,9 mg/ml injektionsvæske, opløsning i fyldt injektionssprøjte

ethypharm - naloxonhydrochlorid (vandfrit) - injektionsvæske, opløsning i fyldt injektionssprøjte - 0,9 mg/ml