欧盟 - 罗马尼亚文 - EMA (European Medicines Agency)

novartis europharm limited  - voretigene neparvovec - leber congenital amaurosis; retinitis pigmentosa - other ophthalmologicals - luxturna este indicat pentru tratamentul pacienților adulți și pacienți copii și adolescenți cu pierderea vederii din cauza moștenit distrofie retinei cauzate de confirmat biallelic rpe65 mutații și care au suficient de viabile celulele retinei.

欧盟 - 罗马尼亚文 - EMA (European Medicines Agency)

novartis europharm limited  - brolucizumab - degenerarea maculară umedă - oftalmologice - beovu este indicat la adulți pentru tratamentul de forma neovasculară (umedă) degenerescenta maculara legata de varsta (amd).

欧盟 - 罗马尼亚文 - EMA (European Medicines Agency)

novartis europharm limited - indacaterol, glycopyrronium bromide, mometasone - astm - medicamente pentru afecțiuni obstructive ale căilor respiratorii, - 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.

欧盟 - 罗马尼亚文 - EMA (European Medicines Agency)

novartis europharm limited  - indacaterol, mometasone furoate - astm - medicamente pentru afecțiuni obstructive ale căilor respiratorii, - 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.

欧盟 - 罗马尼亚文 - EMA (European Medicines Agency)

novartis europharm limited - glycopyrronium bromide, indacaterol (acetate), mometasone furoate - astm - medicamente pentru afecțiuni obstructive ale căilor respiratorii, - maintenance treatment of asthma in adults whose disease is not adequately controlled.

欧盟 - 罗马尼亚文 - EMA (European Medicines Agency)

novartis europharm limited - crizanlizumab - anemie, 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.

欧盟 - 罗马尼亚文 - EMA (European Medicines Agency)

novartis europharm limited - inclisiran - hypercholesterolemia; dyslipidemias - agenți de modificare a lipidelor - 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.

欧盟 - 罗马尼亚文 - EMA (European Medicines Agency)

novartis europharm limited  - capmatinib dihydrochloride monohydrate - carcinom, pulmonar non-celulă mică - agenți antineoplazici - 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.

欧盟 - 罗马尼亚文 - EMA (European Medicines Agency)

novartis europharm limited  - gozetotide - radionuclide imaging - produse radiofarmaceutice de diagnosticare - acest medicament este destinat exclusiv diagnosticului. 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.

欧盟 - 罗马尼亚文 - EMA (European Medicines Agency)

novartis europharm limited  - lutetium (177lu) vipivotide tetraxetan - neoplasmele prostatice, rezistent la castrare - produse radiofarmaceutice terapeutice - pluvicto in combination with androgen deprivation therapy (adt) with or without androgen receptor (ar) pathway inhibition is indicated for the treatment of adult patients with progressive prostate-specific membrane antigen (psma)-positive metastatic castration-resistant prostate cancer (mcrpc) who have been treated with ar pathway inhibition and taxane based chemotherapy.