Gefitinib Mylan ইউরোপীয় ইউনিয়ন - নরওয়েজীয় - EMA (European Medicines Agency)

gefitinib mylan

mylan pharmaceuticals limited - gefitinib - karsinom, ikke-småcellet lunge - antineoplastic agents, protein kinase inhibitors - gefitinib mylan er indisert som monoterapi for behandling av voksne pasienter med lokalt avansert eller metastatisk ikke‑liten celle lunge kreft (nsclc) med aktiverende mutasjoner i egfr‑tk.

Iressa ইউরোপীয় ইউনিয়ন - নরওয়েজীয় - EMA (European Medicines Agency)

iressa

astrazeneca ab - gefitinib - karsinom, ikke-småcellet lunge - antineoplastiske midler - iressa er indisert for behandling av voksne pasienter med lokalt avansert eller metastatisk ikke-liten celle lunge kreft med aktiverende mutasjoner av epidermal vekst-faktor-reseptor tyrosin kinase.

Adempas ইউরোপীয় ইউনিয়ন - নরওয়েজীয় - 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.

Zelboraf ইউরোপীয় ইউনিয়ন - নরওয়েজীয় - 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.

Rimactazid 150 mg / 75 mg নরওয়ে - নরওয়েজীয় - Statens legemiddelverk

rimactazid 150 mg / 75 mg

sandoz - københavn - rifampicin / isoniazid - tablett, filmdrasjert - 150 mg / 75 mg

Rimstar নরওয়ে - নরওয়েজীয় - Statens legemiddelverk

rimstar

sandoz - københavn - rifampicin / isoniazid / pyrazinamid / etambutolhydroklorid - tablett, filmdrasjert - 150 mg / 75 mg / 400 mg / 275 mg