Rivaroxaban Viatris (previously Rivaroxaban Mylan) Evropská unie - čeština - 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 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.

ALERGIMED 5MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

alergimed 5mg potahovaná tableta

medreg s.r.o., praha array - 16445 levocetirizin-dihydrochlorid - potahovaná tableta - 5mg - levocetirizin

DICLOFENAC TEVA 10MG/G Gel Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

diclofenac teva 10mg/g gel

teva b.v., haarlem nizozemsko - 9666 diklofenak-diethylamin - gel - 10mg/g - diklofenak

Varuby Evropská unie - čeština - EMA (European Medicines Agency)

varuby

tesaro bio netherlands b.v. - roupitant - vomiting; nausea; cancer - antiemetika a přípravky proti nevolnosti, - prevenci opožděné nevolnosti a zvracení spojenými s vysoce a středně emetogenní chemoterapii nádorů dospělých. varuby se podává jako součást kombinované terapie.

XPHE JUNIOR SE POR PLV SUS 1X500G Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

xphe junior se por plv sus 1x500g

potraviny pro zvlÁŠtnÍ lÉkaŘskÉ ÚČely (pzlÚ) (ČeskÁ atc skupina)

XPHE KID SE POR PLV SUS 1X500G Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

xphe kid se por plv sus 1x500g

potraviny pro zvlÁŠtnÍ lÉkaŘskÉ ÚČely (pzlÚ) (ČeskÁ atc skupina)

OMEPRAZOL AUROVITAS 20MG Enterosolventní tvrdá tobolka Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

omeprazol aurovitas 20mg enterosolventní tvrdá tobolka

laboratorios liconsa, s.a., madrid array - 8940 omeprazol - enterosolventní tvrdá tobolka - 20mg - omeprazol