Европска Унија - Италијански - EMA (European Medicines Agency)

mylan s.a.s - ritonavir - infezioni da hiv - antivirali per uso sistemico - ritonavir è indicato in combinazione con altri agenti antiretrovirali per il trattamento di pazienti con infezione da hiv 1 (adulti e bambini di età pari o superiore ai 2 anni).

Европска Унија - Италијански - EMA (European Medicines Agency)

mylan ireland limited - il triossido di arsenico - leucemia, promielocitica, acuta - agenti antineoplastici - il triossido di arsenico mylan è indicato per l'induzione della remissione e di consolidamento in pazienti adulti con:- di nuova diagnosi in basso a intermedio rischio di leucemia promielocitica acuta (apl) (numero di globuli bianchi, ≤ 10 x 103/µl) in combinazione con acido all trans retinoico (atra)- recidivato/refrattario leucemia promielocitica acuta (apl) (precedente trattamento che deve aver incluso un retinoide e chemioterapia), caratterizzata dalla presenza di t(15;17) traslocazione e/o la presenza di leucemia promielocitica/recettore dell'acido retinoico alfa (pml/rar alfa) gene. il tasso di risposta di altri mieloide acuta leucemia sottotipi di triossido di arsenico non ha beenexamined.

Европска Унија - Италијански - EMA (European Medicines Agency)

mylan ireland limited - rivaroxaban - venous thromboembolism; pulmonary embolism; acute coronary syndrome; stroke; coronary artery disease; peripheral arterial disease; atrial fibrillation - agenti antitrombotici - rivaroxaban mylan co-administered with acetylsalicylic acid (asa) alone or with asa plus clopidogrel or ticlopidine, is indicated for the prevention of atherothrombotic events in adult patients after an acute coronary syndrome (acs) with elevated cardiac biomarkers.  rivaroxaban mylan co-administered with acetylsalicylic acid (asa), is indicated for the prevention of atherothrombotic events in adult patients with coronary artery disease (cad) or symptomatic peripheral artery disease (pad) at high risk of ischaemic events.  ------prevention of venous thromboembolism (vte) in adult patients undergoing elective hip or knee replacement surgery.  treatment of deep vein thrombosis (dvt) and pulmonary embolism (pe), and prevention of recurrent dvt and pe in adults. -------adults prevention of stroke and systemic embolism in adult   patients with non-valvular atrial fibrillation with one or more risk factors, such as congestive heart failure, hypertension, age ≥ 75 years, diabetes mellitus, prior stroke or transient ischaemic attack. paediatric population treatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing from 30 kg to 50 kg after at least 5 days of initial parenteral anticoagulation treatment. paediatric population treatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing more than 50 kg after at least 5 days of initial parenteral anticoagulation treatment.

Европска Унија - Италијански - EMA (European Medicines Agency)

mylan ireland limited - sugammadex sodium - blocco neuromuscolare - tutti gli altri prodotti terapeutici - reversal of neuromuscular blockade induced by   rocuronium or vecuronium in adults. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Европска Унија - Италијански - EMA (European Medicines Agency)

mylan ireland limited - sitagliptin hydrochloride monohydrate, metformin hydrochloride - diabete mellito, tipo 2 - farmaci usati nel diabete - for adult patients with type 2 diabetes mellitus:sitagliptin/metformin hydrochloride mylan is indicated as an adjunct to diet and exercise to improve glycaemic control in patients inadequately controlled on their maximal tolerated dose of metformin alone or those already being treated with the combination of sitagliptin and metformin. sitagliptin/metformin hydrochloride mylan is indicated in combination with a sulphonylurea (i. , triplice terapia di associazione) in aggiunta alla dieta e all'esercizio fisico in pazienti non adeguatamente controllati il loro dosaggio massimo tollerato di metformina ed una sulfonilurea. sitagliptin/metformin hydrochloride mylan is indicated as triple combination therapy with a peroxisome proliferator-activated receptor gamma (pparg) agonist (i. , a thiazolidinedione) as an adjunct to diet and exercise in patients inadequately controlled on their maximal tolerated dose of metformin and a pparg agonist. sitagliptin/metformin hydrochloride mylan is also indicated as add-on to insulin (i. , triple combination therapy) as an adjunct to diet and exercise to improve glycaemic control in patients when stable dose of insulin and metformin alone do not provide adequate glycaemic control.

Швајцарска - Италијански - Swissmedic (Swiss Agency for Therapeutic Products)

viatris pharma gmbh - moxonidinum - compresse rivestite con film - moxonidinum 0.2 mg, lactosum monohydricum 95.8 mg, povidonum k 25, crospovidonum, magnesii stearas, Überzug: hypromellosum, ethylcellulosum, macrogolum 6000, talcum, e 171, e 172 (rubrum), pro compresso obducto. - antihypertonicum - synthetika

Швајцарска - Италијански - Swissmedic (Swiss Agency for Therapeutic Products)

viatris pharma gmbh - moxonidinum - compresse rivestite con film - moxonidinum 0.3 mg, lactosum monohydricum 95.7 mg, povidonum k 25, crospovidonum, magnesii stearas, Überzug: hypromellosum, ethylcellulosum, macrogolum 6000, talcum, e 171, e 172 (rubrum), pro compresso obducto. - antihypertonicum - synthetika

Швајцарска - Италијански - Swissmedic (Swiss Agency for Therapeutic Products)

viatris pharma gmbh - moxonidinum - compresse rivestite con film - moxonidinum 0.4 mg, lactosum monohydricum 95.60 mg, povidonum k 25, crospovidonum, magnesii stearas, Überzug: hypromellosum, ethylcellulosum, macrogolum 6000, talcum, e 171, e 172 (rubrum), pro compresso obducto. - antihypertonicum - synthetika

Швајцарска - Италијански - Swissmedic (Swiss Agency for Therapeutic Products)

viatris pharma gmbh - exemestanum - compresse rivestite con film - exemestanum 25 mg, mannitolum, hypromellosum, crospovidonum, polysorbatum 80, cellulosum microcristallinum, carboxymethylamylum natricum a, magnesii stearas, silica colloidalis anhydrica, Überzug: carmellosum natricum, maltodextrinum, glucosum monohydricum 0.441 mg, acidum stearicum, e 171, e 172 (flavum), pro compresso obducto corresp. natrium 0.15 - 0.25 mg. - 2nd e 3rd line terapia avanzata di mamma-ca nelle pazienti in postmenopausa - synthetika

Швајцарска - Италијански - Swissmedic (Swiss Agency for Therapeutic Products)

viatris pharma gmbh - emtricitabinum, tenofovirum disoproxilum - compresse rivestite con film - emtricitabinum 200 mg, tenofovirum disoproxilum 245 mg ut tenofoviri disoproxili maleas 300 mg, cellulosum microcristallinum, hydroxypropylcellulosum substitutum humile, silica colloidalis anhydrica, lactosum monohydricum 82.79 mg, magnesii stearas, e 172 (rubrum), Überzug: lactosum monohydricum 10.78 mg, hypromellosum, triacetinum, e 133, e 171, e 172 (flavum), pro compresso obducto. - l'infezione da hiv - synthetika