Table 1.
Indication | Rivaroxaban dose regimen | Dose adjustments | Duration |
---|---|---|---|
Prevention of stroke and systemic embolism in patients with atrial fibrillation at moderate to high stroke riska | 20 mg od | 15 mg od in patients with CrCl 15–49 mL/min | Ongoing provided the risk of stroke outweighs the risk of bleedingb |
Prevention of venous thromboembolism in patients who have undergone major hip or knee replacement surgery | 10 mg od | None | 12–14 days after knee replacement 35 days after hip replacement |
Treatment of deep vein thrombosis and pulmonary embolism and prevention of recurrent venous thromboembolism |
15 mg bid for 3 weeks (acute treatment) 20 mg od thereafter (secondary prevention) |
Nonec | Generally at least 3 months but to continue as long as the risk of recurrent VTE outweighs the risk of bleedingd |
Prevention of atherothrombotic events in patients with recent acute coronary syndrome and elevated cardiac biomarkers (Europe only)e | 2.5 mg bid in combination with single or dual antiplatelet therapyf | None | Based on the individual patient’s risk of ischemic events against bleeding risks |
bid twice daily, CrCl creatinine clearance, od once daily
aCHA2DS2-VASc score recommended to assess stroke risk [80]
bHAS-BLED score may be useful for determining bleeding risk [80]
cNo routine dose reduction but consider 15 mg od in patients with moderate renal impairment (CrCl 30–49 mL/min) with a high bleeding risk (Europe only) [1]
dClinical risk scores and risk factors for bleeding can be useful for assessment [49, 50]
eCardiac biomarkers are troponin or creatinine kinase-MB [1]
fAcetylsalicylic acid with or without a thienopyridine (clopidogrel or ticlopidine) [1]