Warfarin Dose Calculator
INR-based warfarin dose adjustment with initiation dosing, drug/food interaction alerts, and evidence-based clinical guidance.
INR-Based Dose Adjustment
Warfarin Initiation (Crowther Protocol)
Initiation Protocol Overview
| Day | 5 mg Protocol | 10 mg Protocol |
|---|---|---|
| Day 1–2 | 5 mg daily | 10 mg daily |
| Day 3 | Check INR → adjust dose per algorithm | |
| Day 4–5 | Adjust based on INR; continue checking | |
| Day 5–7 | Check INR; aim for therapeutic range by days 5–7 | |
INR Monitoring Timeline
- Initiation (days 1–7): Check INR every 2–3 days
- Early stabilization (weeks 1–4): Check INR every 3–7 days
- Stable dose (weeks 4–12): Check INR every 1–2 weeks
- Established therapy: Check INR every 4–6 weeks if stable
- After any change: Recheck INR in 3–7 days (new meds, diet changes, dose adjustment)
Disclaimer: For educational purposes only. Not a substitute for clinical judgment. Warfarin dosing is highly individualized — always consider patient-specific factors including age, genetics, renal/hepatic function, nutritional status, and concomitant medications. Follow your institution's anticoagulation management protocols.
About This Tool
What Is Warfarin Dose Adjustment?
Warfarin (Coumadin) is a vitamin K antagonist anticoagulant used to prevent and treat thromboembolic events including stroke in atrial fibrillation, deep vein thrombosis (DVT), pulmonary embolism (PE), and mechanical heart valve thrombosis. Because warfarin has a narrow therapeutic index and highly variable pharmacokinetics, dosing must be individualized and guided by regular INR (International Normalized Ratio) monitoring.
How INR-Based Dose Adjustment Works
The INR measures the degree of anticoagulation — a higher INR means more anticoagulation. The goal is to maintain the INR within a target range that balances stroke/clot prevention against bleeding risk. Most indications target an INR of 2.0–3.0; mechanical heart valves (especially mitral) target 2.5–3.5. When INR falls outside the target, the weekly warfarin dose is adjusted by a percentage, typically 5–20%, depending on how far the INR deviates.
Who Needs Warfarin Dose Monitoring?
All patients taking warfarin require regular INR monitoring. This is especially critical during initiation (first 1–4 weeks), after dose changes, when new medications are started or stopped, during acute illness, and with significant dietary changes. Patients at highest risk for instability include the elderly, those with liver disease, heart failure, cancer, or multiple interacting medications.
🔑 Clinical Pearls
- Time in Therapeutic Range (TTR) is the key quality metric — aim for TTR >65%. Below this, consider switching to a DOAC if eligible.
- Warfarin has a 36–42 hour half-life — dose changes take 3–5 days to reach new steady state. Don't recheck INR too soon after adjustment.
- Genetic variability: CYP2C9 poor metabolizers and VKORC1 variants may need 50–75% lower doses. Consider genotyping in patients with unexpected sensitivity.
- Consistency over avoidance: Patients should not avoid vitamin K–rich foods; rather, they should maintain a consistent diet so the warfarin dose can be calibrated accordingly.
- The biggest interactor is amiodarone — when starting amiodarone, empirically reduce warfarin by 30–50% and check INR in 3–5 days.
Warfarin Initiation: The Crowther Protocol
The Crowther protocol provides evidence-based guidance for initiating warfarin therapy. A 5 mg starting dose is recommended for most patients, particularly the elderly (>60), malnourished patients, those with liver disease or heart failure, and patients on interacting drugs. A 10 mg loading dose may be used in younger, otherwise healthy patients without risk factors for warfarin sensitivity. INR should be checked on day 3, and the dose adjusted according to a nomogram.
When to Consider Alternatives to Warfarin
DOACs (apixaban, rivaroxaban, edoxaban, dabigatran) are preferred over warfarin for non-valvular AF and VTE in most patients per current guidelines. Warfarin remains the only appropriate anticoagulant for mechanical heart valves, moderate-to-severe mitral stenosis, and antiphospholipid syndrome (triple-positive). Consider switching to a DOAC if time in therapeutic range is consistently below 65%.
Key References
- Holbrook AM, et al. Systematic overview of warfarin and its drug and food interactions. Arch Intern Med. 2005;165(10):1095–1106.
- Ageno W, et al. Oral anticoagulant therapy — ACCP Evidence-Based Guidelines. Chest. 2012;141(2 Suppl):e44S–e88S.
- Stevens SM, et al. Antithrombotic therapy for VTE disease: CHEST Guideline Update. Chest. 2021;160(6):e545–e608.
- Crowther MA, et al. A randomized trial comparing 5-mg and 10-mg warfarin loading doses. Arch Intern Med. 1999;159(1):46–48.
- Witt DM, et al. Clinical pharmacy anticoagulation service outcomes. Chest. 2005;127(5):1515–1522.
Formula last verified: February 2026