Европейски съюз - естонски - EMA (European Medicines Agency)

novartis europharm limited - tegaserod - Ärritunud soole sündroom - funktsionaalsete seedetrakti häirete ravimid - zelnorm on näidustatud korduvate sümptomitega lühiajaline ravi naistel Ärritatud soole sündroom (ibs), kelle domineeriv soole harjumus on kõhukinnisus, mis on seotud kõhuvalu/ebamugavustunne või kõhupuhitus (vt lõik 4.

Европейски съюз - естонски - EMA (European Medicines Agency)

novartis europharm limited  - brolucizumab - märg macula degeneration - oftalmoloogilised vahendid - beovu on näidustatud täiskasvanute raviks neovascular (märg) vanusega seotud makuladegeneratsiooni (amd).

Европейски съюз - естонски - EMA (European Medicines Agency)

novartis europharm limited  - onasemnogene abeparvovec - lihase atroofia, spinaalne - muud lihas-skeleti süsteemi häirete ravimid - zolgensma on näidustatud ravi:patsiendid, kellel on 5q seljaaju lihaste atroofia (sma) koos bi-allelic mutatsioon smn1 geeni-ja kliinilise diagnoosi akti liik 1, orpatients koos 5q sma koos bi-allelic mutatsioon smn1 geeni-ja kuni 3 koopiad smn2 geenide.

Европейски съюз - естонски - EMA (European Medicines Agency)

novartis europharm limited - indacaterol, glycopyrronium bromide, mometasone - astma - ravimid hingamisteede obstruktiivsete haiguste, - enerzair breezhaler is indicated as a maintenance treatment of asthma in adult patients not adequately controlled with a maintenance combination of a long acting beta2 agonist and a high dose of an inhaled corticosteroid who experienced one or more asthma exacerbations in the previous year.

Европейски съюз - естонски - EMA (European Medicines Agency)

novartis europharm limited  - indacaterol, mometasone furoate - astma - ravimid hingamisteede obstruktiivsete haiguste, - 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.

Европейски съюз - естонски - EMA (European Medicines Agency)

novartis europharm limited - glycopyrronium bromide, indacaterol (acetate), mometasone furoate - astma - ravimid hingamisteede obstruktiivsete haiguste, - maintenance treatment of asthma in adults whose disease is not adequately controlled.

Европейски съюз - естонски - EMA (European Medicines Agency)

novartis europharm limited - crizanlizumab - aneemia, sickle cell - 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.

Европейски съюз - естонски - EMA (European Medicines Agency)

novartis europharm limited - inclisiran - hypercholesterolemia; dyslipidemias - lipiidi modifitseerivad ained - leqvio is indicated in adults with primary hypercholesterolaemia (heterozygous familial and non-familial) or mixed dyslipidaemia, as an adjunct to diet:in combination with a statin or statin with other lipid-lowering therapies in patients unable to reach ldl-c goals with the maximum tolerated dose of a statin, oralone or in combination with other lipid-lowering therapies in patients who are statin-intolerant, or for whom a statin is contraindicated.

Европейски съюз - естонски - EMA (European Medicines Agency)

novartis europharm limited  - capmatinib dihydrochloride monohydrate - kartsinoom, mitteväikerakk-kopsu - antineoplastilised ained - 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.

Европейски съюз - естонски - EMA (European Medicines Agency)

novartis europharm limited  - gozetotide - radionukliidi pildistamine - diagnostilised radiofarmatseutilised ühendid - see ravim on mõeldud ainult diagnostiliseks kasutamiseks. locametz, after radiolabelling with gallium 68, is indicated for the detection of prostate specific membrane antigen (psma) positive lesions with positron emission tomography (pet) in adults with prostate cancer (pca) in the following clinical settings:primary staging of patients with high risk pca prior to primary curative therapy,suspected pca recurrence in patients with increasing levels of serum prostate specific antigen (psa) after primary curative therapy,identification of patients with psma positive progressive metastatic castration resistant prostate cancer (mcrpc) for whom psma targeted therapy is indicated (see section 4.