What is the recommended infusion protocol for Amiodarone (antiarrhythmic medication)?

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Last updated: December 4, 2025View editorial policy

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Amiodarone Infusion Protocol

For life-threatening ventricular arrhythmias, administer an initial loading dose of 150 mg IV over 10 minutes, followed by 1 mg/min for 6 hours, then 0.5 mg/min for the remaining 18 hours, with a maximum total dose of 2.2 g over 24 hours. 1, 2

Initial Loading Protocol

The FDA-approved dosing regimen delivers approximately 1000 mg over the first 24 hours using this three-phase approach: 2

  • Rapid loading bolus: 150 mg IV over 10 minutes (can be repeated once if VF/pulseless VT persists) 1, 2
  • Slow loading infusion: 1 mg/min for 6 hours (360 mg total) 1, 2
  • Maintenance infusion: 0.5 mg/min for the remaining 18 hours (540 mg total) 1, 2

For cardiac arrest with VF/pulseless VT unresponsive to defibrillation and epinephrine, use 300 mg IV/IO bolus over 10 minutes, with a second 150 mg bolus if the rhythm persists. 3

Breakthrough Arrhythmia Management

If breakthrough episodes of hemodynamically unstable VT or VF occur during maintenance infusion: 2

  • Administer supplemental 150 mg boluses mixed in 100 mL D5W over 10 minutes 2
  • The maintenance infusion rate may be increased to achieve effective arrhythmia suppression 2
  • Do not exceed 2.2 g total dose in 24 hours 1, 2

Administration Requirements

Critical administration details to prevent complications: 2

  • Use a volumetric infusion pump (drop counter sets can underdose by up to 30%) 2
  • Administer through a central venous catheter whenever possible 2
  • Use an in-line filter during administration 2
  • For concentrations >2 mg/mL, a central line is mandatory 2
  • For infusions >1 hour, do not exceed 2 mg/mL concentration unless using a central line (higher concentrations cause severe peripheral vein phlebitis) 1, 2
  • Administer in glass or polyolefin bottles containing D5W for infusions exceeding 2 hours 2
  • Never use evacuated glass containers (causes precipitation) 2

Monitoring During Infusion

Watch closely for these dose-related adverse effects: 1, 4

  • Hypotension (occurs in 16% of IV patients; most common adverse effect) 1, 4
  • Bradycardia (occurs in 4.9% of IV patients) 4
  • AV block and heart block 1, 4
  • QT prolongation (common but rarely causes torsades de pointes) 4
  • Phlebitis at infusion site 1

The initial infusion rate should never exceed 30 mg/min to minimize hypotension risk. 2

Extended Maintenance Therapy

After the first 24 hours: 2

  • Continue 0.5 mg/min (720 mg per 24 hours) using 1-6 mg/mL concentration 2
  • Maintenance infusion can continue for 2-3 weeks regardless of age, renal function, or left ventricular function 2
  • Limited experience exists beyond 3 weeks of continuous IV therapy 2

Common Pitfalls to Avoid

Do not use faster infusion rates or higher concentrations than recommended - this has resulted in hepatocellular necrosis, acute renal failure, and death. 2 Mean daily doses above 2100 mg are associated with increased hypotension risk. 2

The drug shows considerable interindividual variation in response, requiring close monitoring with dose adjustment. 2 PVC tubing leaches plasticizers (DEHP) when using higher concentrations and lower flow rates, though all clinical experience has been with PVC tubing at the recommended concentrations. 2

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Amiodarone Therapy Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Amiodarone Oral to Intravenous Equivalency

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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