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.

APIXABAN VIATRIS 2,5MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

apixaban viatris 2,5mg potahovaná tableta

viatris limited, dublin array - 17381 apixaban - potahovaná tableta - 2,5mg - apixaban

APIXABAN SANDOZ 2,5MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

apixaban sandoz 2,5mg potahovaná tableta

sandoz s.r.o., praha array - 17381 apixaban - potahovaná tableta - 2,5mg - apixaban

APIXABAN STADA 2,5MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

apixaban stada 2,5mg potahovaná tableta

stada arzneimittel ag, bad vilbel array - 17381 apixaban - potahovaná tableta - 2,5mg - apixaban

APIXABAN TEVA 2,5MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

apixaban teva 2,5mg potahovaná tableta

teva pharmaceuticals cr, s.r.o., praha array - 17381 apixaban - potahovaná tableta - 2,5mg - apixaban

APIXABAN FARMAPROJECTS 2,5MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

apixaban farmaprojects 2,5mg potahovaná tableta

farmaprojects s.a.u., barcelona array - 17381 apixaban - potahovaná tableta - 2,5mg - apixaban

CLOSDERIVE 10MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

closderive 10mg potahovaná tableta

swyssi ag, frankfurt am main array - 17116 rivaroxaban - potahovaná tableta - 10mg - rivaroxaban

CLOSDERIVE 15MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

closderive 15mg potahovaná tableta

swyssi ag, frankfurt am main array - 17116 rivaroxaban - potahovaná tableta - 15mg - rivaroxaban

CLOSDERIVE 20MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

closderive 20mg potahovaná tableta

swyssi ag, frankfurt am main array - 17116 rivaroxaban - potahovaná tableta - 20mg - rivaroxaban

ENKIA 15MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

enkia 15mg potahovaná tableta

medochemie ltd., limassol array - 17116 rivaroxaban - potahovaná tableta - 15mg - rivaroxaban