Rivaroxaban Viatris (previously Rivaroxaban Mylan) Unió Europea - eslovac - EMA (European Medicines Agency)

rivaroxaban viatris (previously rivaroxaban mylan)

mylan ireland limited - rivaroxaban - venous thromboembolism; pulmonary embolism; acute coronary syndrome; stroke; coronary artery disease; peripheral arterial disease; atrial fibrillation - antitrombotické činidlá - 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.

Sugammadex Mylan Unió Europea - eslovac - EMA (European Medicines Agency)

sugammadex mylan

mylan ireland limited - sugammadex sodium - neuromuskulárna blokáda - všetky ostatné terapeutické produkty - 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.

Deferasirox Mylan Unió Europea - eslovac - EMA (European Medicines Agency)

deferasirox mylan

mylan pharmaceuticals limited - deferasirox - iron overload; beta-thalassemia - Žehlička chelatačné činidlá - deferasirox mylan je uvedené forthe liečba chronického preťaženia železom vzhľadom na časté krvné transfúzie (≥7 ml/kg/mesiac balené červených krviniek) u pacientov s beta thalassaemia major vo veku 6 rokov a olderthe liečba chronického preťaženia železom v dôsledku krvnej transfúzie, ak deferoxamínu terapia je kontraindikovaný alebo je nedostatočné v týchto skupín pacientov:v pediatrických pacientov s beta thalassaemia hlavných s preťaženia železom vzhľadom na časté krvné transfúzie (≥7 ml/kg/mesiac balené červených krviniek) vo veku 2 až 5 rokov,u dospelých a pediatrických pacientov s beta thalassaemia hlavných s preťaženia železom kvôli zriedkavé krvné transfúzie (.

Montelukast Mylan 10 mg Eslovàquia - eslovac - ŠÚKL (Štátny ústav pre kontrolu liečiv)

montelukast mylan 10 mg

mylan ireland limited, Írsko - montelukast - 14 - bronchodilatantia, antiasthmatica

Metformin Mylan XR 750 mg Eslovàquia - eslovac - ŠÚKL (Štátny ústav pre kontrolu liečiv)

metformin mylan xr 750 mg

mylan ireland limited, Írsko - metformín - 18 - antidiabetica (vrÁtane inzulÍnu)

Metformin Mylan XR 500 mg Eslovàquia - eslovac - ŠÚKL (Štátny ústav pre kontrolu liečiv)

metformin mylan xr 500 mg

mylan ireland limited, Írsko - metformín - 18 - antidiabetica (vrÁtane inzulÍnu)