What is the recommended oral dosage of amiodarone (PO) for a patient with atrial fibrillation (AFib)?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: January 22, 2026View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Oral Amiodarone Dosing for Atrial Fibrillation

For maintenance of sinus rhythm in atrial fibrillation, start with an oral loading dose of 600 mg daily for one month (or 1000 mg daily for one week), followed by a maintenance dose of 100-400 mg daily, with most patients requiring 200 mg daily long-term. 1

Loading Phase

The loading strategy depends on clinical urgency and setting:

  • Standard outpatient loading: 600 mg daily for approximately one month to achieve a total accumulated dose of approximately 10 grams 1, 2
  • Accelerated inpatient loading: 1000 mg daily for one week, or alternatively 800-1600 mg daily in divided doses until 10 grams total is reached 1, 3
  • For atrial fibrillation specifically: 600-800 mg daily in divided doses until 10 grams total, then transition to maintenance 2, 3

The loading phase is critical because amiodarone has an extremely long half-life (15-100 days, mean 30 days), and the full antiarrhythmic effect takes days to weeks to develop despite adequate serum levels 2, 4

Maintenance Phase

After completing the loading dose:

  • Standard maintenance: 200-400 mg daily 1
  • Low-dose maintenance: 100-200 mg daily may be effective with fewer side effects 1, 3
  • For atrial fibrillation specifically: 200 mg daily is the typical target 2, 3

Low-dose amiodarone (≤200 mg daily) is increasingly preferred as it maintains efficacy while reducing the risk of extracardiac toxicity 1, 5

Efficacy Data

Amiodarone demonstrates superior efficacy compared to other antiarrhythmic agents:

  • 69% maintained sinus rhythm at 16 months versus 39% with propafenone or sotalol in the CTAF study 1
  • 62% remained in sinus rhythm at one year versus 23% with class I agents in the AFFIRM study 1, 2
  • Median time to AF recurrence of 487 days with amiodarone versus 74 days with sotalol 2
  • 79% long-term success rate in patients with refractory AF at mean 21-month follow-up 6

Patient Selection Considerations

Amiodarone is particularly appropriate as a first-line agent in specific populations:

  • Patients with structural heart disease: Left ventricular hypertrophy, heart failure, coronary artery disease, or previous MI, where amiodarone has low proarrhythmic risk 1
  • Reduced ejection fraction: Safe and effective even with LVEF ≤30% 7
  • Contraindications to class IC drugs: When flecainide or propafenone cannot be used 8

However, amiodarone is often considered second-line in patients without structural heart disease due to the risk of extracardiac toxicity 1

Predictors of Success

Factors associated with better outcomes:

  • Shorter duration of AF: Chronic AF >1 year has lower success (57%) but still reasonable efficacy 6
  • Smaller left atrial diameter: Larger atria predict lower conversion rates 6, 7, 8
  • Smaller left ventricular dimensions: Associated with better rhythm control 7

Critical Monitoring Requirements

During Loading Phase

  • Bradycardia and heart block: Occurs in 1-3% on oral therapy 2, 3
  • QT prolongation: Common but rarely causes torsades de pointes 1, 2
  • Hypotension: Particularly with higher loading doses 2, 3
  • ECG monitoring: Daily initially, then weekly during loading 2

Long-Term Monitoring

  • Pulmonary toxicity: Dose-dependent, requires periodic chest imaging 1
  • Thyroid dysfunction: Both hypo- and hyperthyroidism can occur 1
  • Hepatic toxicity: Monitor liver function tests 1
  • Ocular complications: Annual ophthalmologic examination 1
  • Photosensitivity: Counsel patients on sun protection 1

Important Drug Interactions

Amiodarone requires immediate dose adjustments of concomitant medications:

  • Warfarin: Reduce dose by 30-50% and check INR within 3-5 days, as amiodarone significantly increases INR 2, 3
  • Digoxin: Reduce dose by 50% immediately, as amiodarone doubles digoxin levels 2, 3
  • Other rate-control agents: Beta-blockers and calcium channel blockers may need dose reduction as amiodarone provides additional rate control 1, 2

Common Pitfalls to Avoid

  • Inadequate loading: Skipping or abbreviating the loading phase leads to delayed therapeutic effect and early recurrence 4
  • Premature discontinuation: 18% of patients stop amiodarone due to side effects, but many adverse effects are dose-dependent and manageable with dose reduction 1
  • Ignoring drug interactions: Failure to adjust warfarin or digoxin can lead to serious complications 2, 3
  • Expecting immediate effect: Most conversions occur after 6-8 hours, with maximal effects not attained before 90-150 days 4, 8

Additional Benefits

Beyond rhythm control, amiodarone provides:

  • Effective rate control: Often eliminates the need for additional rate-control medications 1
  • Improved quality of life: Associated with fewer AF-related procedures and lower costs 1
  • Improved ventricular function: In heart failure patients, successful rhythm control improves LVEF and reduces BNP levels 7

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Amiodarone Oral to Intravenous Equivalency

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Amiodarone Loading Dose Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Ten years of experience with amiodarone.

American heart journal, 1983

Research

Amiodarone for refractory atrial fibrillation.

The American journal of cardiology, 1986

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.