Unione Europea - italiano - EMA (European Medicines Agency)

novartis europharm limited - vildagliptin - diabete mellito, tipo 2 - farmaci usati nel diabete - vildagliptin is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:as monotherapy in patients in whom metformin is inappropriate due to contraindications or intolerance. in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control (see sections 4. 4, 4. 5 e 5. 1 per i dati disponibili su diverse combinazioni).

Unione Europea - italiano - EMA (European Medicines Agency)

novartis europharm limited - erenumab - emicrania - analgesici - aimovig è indicato per la profilassi dell'emicrania negli adulti che hanno almeno 4 emicrania giorni al mese quando iniziare il trattamento con aimovig.

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 - 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  - 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.

Unione Europea - italiano - EMA (European Medicines Agency)

novartis europharm limited  - lutetium (177lu) vipivotide tetraxetan - prostatica neoplasie, castrazione-resistente - radiofarmaci terapeutici - 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.