Rivaroxaban Viatris (previously Rivaroxaban Mylan)
Land: Den europeiske union
Språk: gresk
Kilde: EMA (European Medicines Agency)
Informasjon til brukeren
(PIL)
13-12-2023
Preparatomtale
(SPC)
13-12-2023
Offentlig vurderingsrapport
(PAR)
21-09-2023
Aktiv ingrediens:
rivaroxaban
Tilgjengelig fra:
Mylan Ireland Limited
ATC-kode:
B01AF01
INN (International Name):
rivaroxaban
Terapeutisk gruppe:
Αντιθρομβωτικοί παράγοντες
Terapeutisk område:
Venous Thromboembolism; Pulmonary Embolism; Acute Coronary Syndrome; Stroke; Coronary Artery Disease; Peripheral Arterial Disease; Atrial Fibrillation
Indikasjoner:
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.
Produkt oppsummering:
Revision: 4
Autorisasjon status:
Εξουσιοδοτημένο
Autorisasjon dato:
2021-11-12
Informasjon til brukeren
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Preparatomtale
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