What is the recommended IV (intravenous) amiodarone loading dose and 24-hour infusion regimen for treating arrhythmias?

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Last updated: November 13, 2025View editorial policy

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IV Amiodarone Loading Dose and 24-Hour Infusion Regimen

For chemical or electrical cardioversion of arrhythmias, administer 150 mg IV over 10 minutes as the loading dose, followed by 1 mg/min infusion for 6 hours (360 mg), then 0.5 mg/min for the remaining 18 hours (540 mg), with a maximum total dose of 2.2 g over 24 hours. 1, 2, 3

Standard Dosing Protocol

The recommended first 24-hour regimen consists of three distinct phases:

  • Loading dose: 150 mg IV over 10 minutes 1, 2, 3
  • Early maintenance: 1 mg/min for 6 hours (total 360 mg) 1, 2, 3
  • Late maintenance: 0.5 mg/min for 18 hours (total 540 mg) 1, 2, 3
  • Total 24-hour dose: Approximately 1050 mg, not to exceed 2.2 g 1, 2, 3

Supplemental Dosing for Breakthrough Arrhythmias

If breakthrough ventricular fibrillation or hemodynamically unstable ventricular tachycardia occurs during the infusion:

  • Administer an additional 150 mg IV bolus over 10 minutes 3
  • Mix in 100 mL D5W to minimize hypotension risk 3
  • This supplemental dose can be repeated as needed while staying within the 2.2 g/24-hour maximum 3

Administration Requirements

Critical administration details to prevent complications:

  • Use a volumetric infusion pump (never drop counters, which can underdose by up to 30%) 3
  • Administer through a central venous catheter whenever possible 2, 3
  • Use an in-line filter during administration 3
  • For concentrations >2 mg/mL, a central line is mandatory to prevent phlebitis 3
  • Maximum initial infusion rate: 30 mg/min 3
  • Prepare in glass or polyolefin bottles with D5W (not evacuated glass containers) 3

Continuation Beyond 24 Hours

After the initial 24 hours, the maintenance infusion can be continued:

  • Continue at 0.5 mg/min (720 mg per 24 hours) 3
  • May increase rate to achieve effective arrhythmia suppression 3
  • Can be safely continued for 2-3 weeks regardless of age, renal function, or left ventricular function 3
  • Mean daily doses above 2100 mg are associated with increased hypotension risk 3

Monitoring Requirements During Infusion

Essential monitoring parameters include:

  • Continuous cardiac monitoring for bradycardia and AV block 2
  • Regular blood pressure monitoring for hypotension (occurs in 16% of patients) 1, 2
  • ECG monitoring for QT prolongation 2
  • Hypotension is the most common serious adverse effect during IV administration 1, 4

Clinical Context and Efficacy

The timing and dose are critical for efficacy:

  • Cardioversion to sinus rhythm typically occurs after 6-8 hours 2
  • Often requires ≥1000 mg total dose for successful conversion 2
  • Conversion rates: 34-69% with bolus-only regimens, 55-95% with bolus plus continuous infusion 2, 5
  • Higher doses (>1500 mg/day) are superior to placebo for recent-onset atrial fibrillation 5

Common Pitfalls to Avoid

  • Do not use drop counter infusion sets - they can underdose by 30% due to altered surface properties 3
  • Do not exceed 3 mg/mL concentration without a central line - peripheral vein phlebitis occurs frequently at higher concentrations 3
  • Do not infuse faster than 30 mg/min initially - rapid infusions have caused hepatocellular necrosis and acute renal failure 3
  • Do not use PVC containers for mixing - incompatibility may cause precipitation 3

Special Populations

Amiodarone is particularly valuable in specific clinical scenarios:

  • Patients with structural heart disease where class IC drugs are contraindicated 2, 5
  • Patients with left ventricular dysfunction 2, 5
  • Hemodynamically stable monomorphic ventricular tachycardia 1
  • Pre-excited atrial arrhythmias with rapid ventricular rates 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Amiodarone Administration Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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.

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