Rivaroxaban
Brand names: Xarelto
Rivaroxaban is a direct oral factor Xa inhibitor (DOAC) for atrial-fibrillation stroke prevention, VTE treatment/prevention and, at low dose, vascular protection.
Adult dose
Dose adjustments
CrCl 15–29 mL/min: use with caution; use not recommended if CrCl <15 mL/min. VTE prevention (surgery): no adjustment for CrCl 30–80 mL/min. DVT/PE treatment: no adjustment for CrCl 50–80 mL/min; for CrCl 15–49 mL/min give 15 mg twice daily for the first 3 weeks, then consider reducing 20 mg once daily to 15 mg once daily if bleeding risk outweighs recurrence risk. Particularly relevant in the elderly, who often have reduced renal function.
Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.
US labelling (FDA)
Reference — US labelling, may differ from UKNonvalvular Atrial Fibrillation : 15 or 20 mg, once daily with food ( 2.1 ) Treatment of DVT and/or PE : 15 mg orally twice daily with food for the first 21 days followed by 20 mg orally once daily with food for the remaining treatment ( 2.1 ) Reduction in the Risk of Recurrence of DVT and/or PE in patients at continued risk for DVT and/or PE : 10 mg once daily with or without food, after at least 6 months of standard anticoagulant treatment ( 2.1 ) Prophylaxis of DVT Following Hip or Knee Replacement Surgery : 10 mg orally once daily with or without food ( 2.1 ) Prophylaxis of VTE in Acutely Ill Medical Patients at Risk for Thromboembolic Complications Not at High Risk of Bleeding : 10 mg …
Source: US FDA prescribing information (openFDA / DailyMed), label dated 2026-01-16. Accessed 2026-06-12. US dosing and indications can differ from UK practice — use UK sources for prescribing decisions.
Contraindications
- Hypersensitivity to the active substance or any excipient
- Active clinically significant bleeding
- Lesion or condition at significant risk of major bleeding (e.g. recent/current GI ulceration, malignant neoplasm at high bleeding risk, recent brain/spinal injury or surgery, recent intracranial haemorrhage, known/suspected oesophageal varices, arteriovenous malformations, vascular aneurysms)
- Concomitant treatment with other anticoagulants, except when switching therapy or for catheter-patency UFH
- Hepatic disease associated with coagulopathy and clinically relevant bleeding risk (including cirrhosis Child-Pugh B and C)
- Pregnancy and breast-feeding
Side effects
- Bleeding (most common)
- Epistaxis
- Gastrointestinal tract haemorrhage
- Anaemia
- Mucosal bleeding (gingival, genitourinary)
Interactions
- Not recommended with systemic azole-antimycotics (ketoconazole, itraconazole, voriconazole, posaconazole) or HIV protease inhibitors (e.g. ritonavir) — strong combined CYP3A4 and P-gp inhibitors that raise rivaroxaban levels and bleeding risk
- Concomitant anticoagulants are contraindicated (except during switching)
- Combined P-gp and strong CYP3A inducers reduce rivaroxaban exposure and may increase thromboembolic risk
Clinical monograph
How it works
It directly inhibits factor Xa.
Prescribing in practice
- The higher treatment doses must be taken with food for adequate absorption; most indications are once daily.
- Dose-reduce in renal impairment and avoid if severe; avoid in significant hepatic impairment with coagulopathy.
- Bleeding is the main risk (andexanet alfa reversal where available).
Monitoring
Monitor renal and hepatic function and the full blood count; watch for bleeding.
Counselling the patient
- Take the higher treatment dose with food, at the same time each day.
- Report any bleeding.
- Tell clinicians you take it before procedures.
Evidence & guidelines
Effective for AF and VTE (ROCKET-AF, EINSTEIN; NICE NG196).
Reference: NICE NG196; EINSTEIN trials; ROCKET-AF trial; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- CHADS₂ Score for AF Stroke Risk · Stroke Risk
- ABC-Bleeding Score for Anticoagulated Atrial Fibrillation · Bleeding Risk
- GARFIELD-AF Risk Score for Atrial Fibrillation · Atrial Fibrillation
- DOAC Score for Selecting Direct Oral Anticoagulant in Non-Valvular AF · Anticoagulation
- ORBIT Bleeding Risk Score for Anticoagulation in AF Patients · Anticoagulation
- SMART Risk Score for Recurrent CVD · Cardiovascular Risk
- Falls Assessment in Older Adults · NICE CG161 2013
- Delirium Outside ICU · NICE CG103
- Comprehensive Geriatric Assessment (CGA) · BGS / NICE
- Delirium Assessment and Management · NICE CG103 2010
- Frailty Recognition and Management · BGS Frailty Framework / NHS NHSE
- Polypharmacy and Medicines Optimisation · STOPP/START v2 2014 / NICE NG5