Direct oral anticoagulant (DOAC) — Factor Xa inhibitor
Pregnancy: Contraindicated — no data on fetal safety; LMWH is the anticoagulant of choice in pregnancy.
Rivaroxaban
Brand names: Xarelto
Adult dose
Dose: AF (stroke prevention): 20 mg once daily with evening meal; VTE treatment: 15 mg BD for 21 days then 20 mg OD
Route: Oral (with food — improves absorption, especially >10 mg doses)
Frequency: Once daily (AF/VTE maintenance); twice daily (VTE initial 21 days)
Max: 20 mg once daily
AF: 20 mg OD with evening meal (15 mg OD if eGFR 15–49). VTE: 15 mg BD with food for 21 days, then 20 mg OD with food. Post-orthopaedic thromboprophylaxis: 10 mg OD for 14–35 days. Reversal: andexanet alfa (expensive, limited availability) or 4-factor PCC.
Paediatric dose
Route: Oral
Frequency: Twice daily
Max: Weight and indication specific
Paediatric VTE (≥2 years, EINSTEIN-Jr): weight-based dosing. Body weight-based equivalents to adult doses used. Specialist haematology guidance required.
Dose adjustments
Renal
AF: reduce to 15 mg OD if eGFR 15–49. Avoid if eGFR <15. VTE: avoid if eGFR <30.
Hepatic
Avoid in moderate-severe hepatic impairment (Child-Pugh B/C).
Clinical pearls
- Meals essential with doses ≥10 mg (bioavailability doubles with food)
- GI bleeding risk higher than apixaban — consider apixaban for patients with prior GI bleed
- Anti-Xa assay can measure levels if needed (not routine)
- Perioperative management: stop 24h before (low bleeding risk) or 48h before (high bleeding risk) procedure
- Reversal: andexanet alfa (AnexXa) licensed but expensive; 4-factor PCC (Octaplex/Beriplex) if andexanet unavailable
Contraindications
- Active significant bleeding
- Lesion at risk of clinically significant bleeding
- Hepatic disease with coagulopathy
- Pregnancy
Side effects
- Bleeding (all sites — GI most common with rivaroxaban)
- Anaemia
- Nausea
- Elevated liver enzymes
- Skin reactions
Interactions
- Strong CYP3A4 and P-gp inhibitors (ketoconazole, ritonavir) — significantly increase rivaroxaban levels (avoid)
- Strong CYP3A4 and P-gp inducers (rifampicin, carbamazepine, phenytoin) — significantly reduce levels (avoid)
- Other anticoagulants and antiplatelet drugs — increased bleeding risk
- NSAIDs — increased GI bleeding risk
Monitoring
- eGFR and LFTs annually
- Signs of bleeding
- Compliance (twice-daily dosing adherence check)
- Haemoglobin
Reference: BNFc; BNF; NICE NG196; EINSTEIN trials; ROCKET-AF trial. Verify against your local formulary and the latest BNF before prescribing.
Related
Curated clinical cross-links plus same-class fallbacks.
Calculators
- 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
Drugs
Pathways
- Falls Assessment in Older Adults · NICE CG161 2013
- 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
- Acute Heart Failure · ESC 2021 Heart Failure Guidelines; NICE NG106