Dacarbazine Lipomed 500 mg Norge - norsk - Statens legemiddelverk

dacarbazine lipomed 500 mg

lipomed gmbh - dakarbazin - pulver til infusjonsvæske, oppløsning - 500 mg

Dacarbazine Lipomed 1000 mg Norge - norsk - Statens legemiddelverk

dacarbazine lipomed 1000 mg

lipomed gmbh - dakarbazin - pulver til infusjonsvæske, oppløsning - 1000 mg

Lumoxiti Den europeiske union - norsk - EMA (European Medicines Agency)

lumoxiti

astrazeneca ab - moxetumomab pasudotox - leukemi, hårete celler - antineoplastiske midler - lumoxiti as monotherapy is indicated for the treatment of adult patients with relapsed or refractory hairy cell leukaemia (hcl) after receiving at least two prior systemic therapies, including treatment with a purine nucleoside analogue (pna).

Adempas Den europeiske union - norsk - EMA (European Medicines Agency)

adempas

bayer ag - riociguat - hypertensjon, pulmonal - antihypertensive midler for pulmonal arteriell hypertensjon - chronic thromboembolic pulmonary hypertension (cteph)adempas is indicated for the treatment of adult patients with who functional class (fc) ii to iii withinoperable cteph,persistent or recurrent cteph after surgical treatment,to improve exercise capacity. pulmonary arterial hypertension (pah)adultsadempas, as monotherapy or in combination with endothelin receptor antagonists, is indicated for the treatment of adult patients with pulmonary arterial hypertension (pah) with who functional class (fc) ii to iii to improve exercise capacity. effekten har vært vist i en pah befolkningen, herunder aetiologies av idiopatisk eller heritable pah eller pah assosiert med bindevev sykdom. paediatricsadempas is indicated for the treatment of pah in paediatric patients aged less than 18 years of age and body weight ≥ 50 kg with who functional class (fc) ii to iii in combination with endothelin receptor antagonists.

Fludarabin Actavis 25 mg/ ml Norge - norsk - Statens legemiddelverk

fludarabin actavis 25 mg/ ml

actavis group ptc ehf - fludarabinfosfat - konsentrat til injeksjons-/infusjonsvæske, oppløsning - 25 mg/ ml

Spravato Den europeiske union - norsk - EMA (European Medicines Agency)

spravato

janssen-cilag international nv - esketamine hydrochloride - depressive lidelse - andre antidepressiva - spravato, i kombinasjon med et ssri eller snri, er indikert for voksne med behandlingsresistent depresjon, som ikke har svart på minst to forskjellige behandlinger med antidepressiva i gjeldende moderat til alvorlig depressiv episode.

Tavlesse Den europeiske union - norsk - EMA (European Medicines Agency)

tavlesse

instituto grifols s.a. - fostamatinib disodium - trombocytopeni - andre systemiske hemostatics - tavlesse er indisert for behandling av kronisk immun trombocytopeni (itp) hos voksne pasienter som er refraktære til andre behandlinger.

Ztalmy Den europeiske union - norsk - EMA (European Medicines Agency)

ztalmy

marinus pharmaceuticals emerald limited - ganaxolone - epileptic syndromes; spasms, infantile - andre antiepileptics - ztalmy is indicated for the adjunctive treatment of epileptic seizures associated with cyclin-dependent kinase-like 5 (cdkl5) deficiency disorder (cdd) in patients 2 to 17 years of age. ztalmy may be continued in patients 18 years of age and older.

Zelboraf Den europeiske union - norsk - EMA (European Medicines Agency)

zelboraf

roche registration gmbh - vemurafenib - melanom - antineoplastiske midler - vemurafenib er indisert i monoterapi for behandling av voksne pasienter med braf-v600-mutasjons-positiv, uoppløselig eller metastatisk melanom.

Sorafenib Accord Den europeiske union - norsk - EMA (European Medicines Agency)

sorafenib accord

accord healthcare s.l.u. - sorafenib tosilate - carcinoma, hepatocellular; carcinoma, renal cell - antineoplastiske midler - hepatocellular carcinomasorafenib accord is indicated for the treatment of hepatocellular carcinoma (see section 5. renal cell carcinomasorafenib accord is indicated for the treatment of patients with advanced renal cell carcinoma who have failed prior interferon-alpha or interleukin-2 based therapy or are considered unsuitable for such therapy.