Unione Europea - italiano - EMA (European Medicines Agency)

novartis europharm limited  - brolucizumab - degenerazione maculare umida - oftalmologici - beovu è indicato negli adulti per il trattamento di neovascolare (bagnato) degenerazione maculare legata all'età (amd).

Unione Europea - italiano - EMA (European Medicines Agency)

novartis europharm limited  - alpelisib - neoplasie al seno - agenti antineoplastici - piqray è indicato in combinazione con fulvestrant per il trattamento di donne in postmenopausa e uomini, con recettore ormonale (hr)-positivo, human epidermal growth factor receptor 2 (her2)-negativo, localmente avanzato o metastatico cancro al seno con una mutazione pik3ca dopo progressione della malattia dopo terapia endocrina come monoterapia (vedere la sezione 5.

Unione Europea - italiano - EMA (European Medicines Agency)

novartis europharm limited - indacaterol, glycopyrronium bromide, mometasone - asma - farmaci per le malattie respiratorie ostruttive, - 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.

Unione Europea - italiano - EMA (European Medicines Agency)

novartis europharm limited  - indacaterol, mometasone furoate - asma - farmaci per le malattie respiratorie ostruttive, - 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.

Unione Europea - italiano - EMA (European Medicines Agency)

novartis europharm limited  - indacaterol acetate, mometasone furoate - asma - farmaci per le malattie respiratorie ostruttive, - atectura 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.

Unione Europea - italiano - EMA (European Medicines Agency)

novartis europharm limited - glycopyrronium bromide, indacaterol (acetate), mometasone furoate - asma - farmaci per le malattie respiratorie ostruttive, - maintenance treatment of asthma in adults whose disease is not adequately controlled.

Unione Europea - italiano - EMA (European Medicines Agency)

novartis europharm limited - crizanlizumab - anemia, falce 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.

Unione Europea - italiano - EMA (European Medicines Agency)

novartis europharm limited  - capmatinib dihydrochloride monohydrate - carcinoma, polmone non a piccole cellule - agenti antineoplastici - 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.

Unione Europea - italiano - EMA (European Medicines Agency)

novartis europharm limited - travoprost - ocular hypertension; glaucoma, open-angle - ophthalmologicals, antiglaucoma preparations and miotics - diminuzione della pressione intraoculare elevata nei pazienti adulti con ipertensione oculare o glaucoma ad angolo aperto (vedere la sezione 5. riduzione della pressione intraoculare elevata in pazienti pediatrici di età compresa tra 3 anni < 18 anni con ipertensione oculare o glaucoma pediatrico.

Unione Europea - italiano - EMA (European Medicines Agency)

novartis europharm limited  - gozetotide - imaging dei radionuclidi - radiofarmaci diagnostici - questo medicinale è solo per uso diagnostico. 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.