Eiropas Savienība - latviešu - EMA (European Medicines Agency)

novartis europharm limited  - indacaterol, mometasone furoate - astma - zāles obstruktīvu elpceļu slimību, - bemrist breezhaler is indicated as a maintenance   treatment of asthma in adults and adolescents 12 years of age and older not adequately controlled with inhaled corticosteroids and inhaled short acting beta2-agonists.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

novartis europharm limited - glycopyrronium bromide, indacaterol (acetate), mometasone furoate - astma - zāles obstruktīvu elpceļu slimību, - maintenance treatment of asthma in adults whose disease is not adequately controlled.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

novartis europharm limited - crizanlizumab - anēmija, sirpjveida šūna - other hematological agents - adakveo is indicated for the prevention of recurrent vaso occlusive crises (vocs) in sickle cell disease patients aged 16 years and older. it can be given as an add on therapy to hydroxyurea/hydroxycarbamide (hu/hc) or as monotherapy in patients for whom hu/hc is inappropriate or inadequate.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

novartis ireland ltd - ofatumumabs - multiplā skleroze, recidivējoši-pārskaitot - immunosuppressant - kesimpta is indicated for the treatment of adult patients with relapsing forms of multiple sclerosis (rms) with active disease defined by clinical or imaging features (see section 5.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

novartis europharm limited  - capmatinib dihydrochloride monohydrate - karcinoma, nesīkšūnu plaušas - antineoplastiski līdzekļi - tabrecta 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.

Latvija - latviešu - Zāļu valsts aģentūra

novartis pharma gmbh, germany - klomipramīna hidrohlorīds - apvalkotās tabletes - 10 mg

Latvija - latviešu - Zāļu valsts aģentūra

novartis pharma gmbh, germany - oktreotīds - Šķīdums injekcijām/infūzijām - 0,1 mg/ml

Latvija - latviešu - Zāļu valsts aģentūra

novartis s.r.o., czech republic - tizanidīns - tablete - 4 mg

Latvija - latviešu - Zāļu valsts aģentūra

novartis (hellas) a.e.b.e., greece - oktreotīds - Šķīdums injekcijām/infūzijām - 0,1 mg/ml

Latvija - latviešu - Zāļu valsts aģentūra

novartis pharma gmbh, germany - diklofenaka nātrija sāls - Šķīdums injekcijām - 75 mg/3 ml