Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

mylan ireland limited, dublin array - 14895 sodnÁ sŮl montelukastu - Žvýkací tableta - 5mg - montelukast

Evropská unie - čeština - EMA (European Medicines Agency)

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

Evropská unie - čeština - EMA (European Medicines Agency)

mylan ireland limited - sugammadex sodium - neuromuskulární blokáda - všechny ostatní terapeutické přípravky - 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.

Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

mylan ireland limited, dublin array - 14175 trihydrÁt natrium-alendronÁtu; 402 cholekalciferol - tableta - 70mg/2800iu - kyselina alendronovÁ a cholekalciferol

Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

mylan ireland limited, dublin array - 14175 trihydrÁt natrium-alendronÁtu; 402 cholekalciferol - tableta - 70mg/5600iu - kyselina alendronovÁ a cholekalciferol

Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

mylan ireland limited, dublin array - 17338 atomoxetin-hydrochlorid - tvrdá tobolka - 10mg - atomoxetin

Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

mylan ireland limited, dublin array - 17338 atomoxetin-hydrochlorid - tvrdá tobolka - 100mg - atomoxetin

Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

mylan ireland limited, dublin array - 17338 atomoxetin-hydrochlorid - tvrdá tobolka - 18mg - atomoxetin

Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

mylan ireland limited, dublin array - 17338 atomoxetin-hydrochlorid - tvrdá tobolka - 25mg - atomoxetin

Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

mylan ireland limited, dublin array - 17338 atomoxetin-hydrochlorid - tvrdá tobolka - 40mg - atomoxetin