Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

aurobindo pharma b.v. baarnsche dijk 1 3741 ln baarn - rivaroxaban 20 mg/stuk ; rivaroxaban 15 mg/stuk - filmomhulde tablet - cellulose, microkristallijn (e 460) ; croscarmellose natrium (e 468) ; hypromellose, type 2910 (3 - 15 mpa.s) (e 464) ; ijzeroxide rood (e 172) ; lactose 1-water ; macrogol 3350 ; magnesiumstearaat (e 470b) ; natriumlaurilsulfaat (e 487) ; polyvinylalcohol, gedeeltelijk gehydrolyseerd (e1203) ; talk (e 553 b) ; titaandioxide (e 171) - rivaroxaban

Europese Unie - Nederlands - EMA (European Medicines Agency)

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

België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

sandoz sa-nv - rivaroxaban 15 mg - filmomhulde tablet - 15 mg - rivaroxaban 15 mg - rivaroxaban

België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

sandoz sa-nv - rivaroxaban 20 mg - filmomhulde tablet - 20 mg - rivaroxaban 20 mg - rivaroxaban

België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

sandoz sa-nv - rivaroxaban 10 mg - filmomhulde tablet - 10 mg - rivaroxaban 10 mg - rivaroxaban

België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

sandoz gmbh - rivaroxaban 15 mg - filmomhulde tablet - 15 mg - rivaroxaban 15 mg - rivaroxaban

België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

sandoz gmbh - rivaroxaban 20 mg - filmomhulde tablet - 20 mg - rivaroxaban 20 mg - rivaroxaban

België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

krka d.d. novo mesto d.d. - rivaroxaban 2,5 mg - filmomhulde tablet - 2,5 mg - rivaroxaban 2.5 mg - rivaroxaban

België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

krka d.d. novo mesto d.d. - rivaroxaban 10 mg - filmomhulde tablet - 10 mg - rivaroxaban 10 mg - rivaroxaban

België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

krka d.d. novo mesto d.d. - rivaroxaban 15 mg - filmomhulde tablet - 15 mg - rivaroxaban 15 mg - rivaroxaban