How to administer a Cordarone (Amiodarone) drip?

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Last updated: January 27, 2026View editorial policy

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How to Administer Cordarone (Amiodarone) Drip

For life-threatening ventricular arrhythmias, administer amiodarone as a 150 mg IV bolus over 10 minutes, followed by 1 mg/min for 6 hours, then 0.5 mg/min for the remaining 18 hours (total ~1,050 mg over 24 hours). 1, 2, 3

Initial Loading Protocol

Rapid Bolus Dose

  • Give 150 mg IV diluted in 100 mL D5W over 10 minutes for sustained monomorphic VT without severe hemodynamic compromise 1, 2, 3
  • For cardiac arrest with VF/pulseless VT unresponsive to defibrillation and epinephrine, use 300 mg IV/IO bolus, with a second 150 mg bolus if rhythm persists 2
  • Do not exceed an initial infusion rate of 30 mg/min 3

Maintenance Infusion Phases

First 6 hours: 1 mg/min (360 mg total) 1, 2, 3

Next 18 hours: 0.5 mg/min (540 mg total) 1, 2, 3

After 24 hours: Continue 0.5 mg/min (720 mg per 24 hours) for up to 2-3 weeks 3

Supplemental Dosing

  • For breakthrough VF or hemodynamically unstable VT, give 150 mg supplemental infusions (mixed in 100 mL D5W over 10 minutes) 3
  • The maintenance infusion rate may be increased to achieve effective arrhythmia suppression, but mean daily doses above 2,100 mg are associated with increased risk of hypotension 3

Critical Administration Requirements

Vascular Access and Concentration

  • Use a central venous catheter whenever possible 2, 3
  • For concentrations >2 mg/mL, a central line is mandatory 2, 3
  • For infusions >1 hour, do not exceed 2 mg/mL concentration unless using a central line, as peripheral vein phlebitis occurs frequently with higher concentrations 2, 3
  • Use an in-line filter during administration 3

Equipment and Solutions

  • Must use a volumetric infusion pump (not drop counters, which can underdose by up to 30%) 3
  • Administer in glass or polyolefin bottles containing D5W for infusions exceeding 2 hours 3
  • Do not use evacuated glass containers for admixing (may cause precipitation) 3
  • PVC tubing is acceptable (all clinical experience used PVC), though it leaches plasticizers including DEHP 3

Mandatory Monitoring During Infusion

Continuous ECG Monitoring

Monitor for the following dose-related adverse effects throughout the infusion 2, 4:

  • Hypotension (occurs in 16% of IV patients) 2, 4
  • Bradycardia (occurs in 4.9% of IV patients) 2, 4
  • AV block and heart block 2, 4
  • QT prolongation 2, 4

Vital Sign Parameters

  • Stop or slow infusion if:
    • Systolic blood pressure falls below 100 mm Hg 1
    • Heart rate drops below 50 bpm 1
  • Monitor for phlebitis at infusion site 2

Absolute Contraindications

Do not administer amiodarone without a functioning pacemaker in patients with: 2, 4

  • Second- or third-degree AV block 2, 4
  • Sick sinus syndrome 2
  • Severe sinus node dysfunction 2

Additional contraindications: 2

  • Acute inflammatory lung disease 2
  • Patients who have had a heart transplant 2

Critical Drug Interactions

Before Starting Infusion

Assess for concomitant medications that increase bradycardia risk 4:

  • Beta-blockers (create additive AV nodal suppression) 4
  • Calcium channel blockers (substantially increase risk of heart block during bolus) 4
  • Digoxin (reduce dose by 50% when starting amiodarone, as levels will double) 2, 4

During and After Infusion

  • Warfarin: Reduce dose by 33-50% and monitor INR at least weekly (interaction peaks at 7 weeks) 2
  • Avoid concomitant QT-prolonging drugs without expert consultation 2, 5

Special Populations

Hepatic Dysfunction

  • Use with extreme caution in hepatic dysfunction 2
  • Intravenous amiodarone loading infusions at much higher concentrations and rates than recommended have resulted in hepatocellular necrosis and acute renal failure, leading to death 3

Heart Failure

  • The standard bolus protocol remains appropriate for acute life-threatening arrhythmias in patients with severe heart failure 4
  • Amiodarone does not typically produce clinically significant cardiodepression in patients with left ventricular dysfunction 4

Elderly Patients

  • Dosing varies considerably depending on age, weight, and hepatic and renal function 1
  • Clinical monitoring is particularly important when changing to oral therapy 3

Transitioning to Oral Amiodarone

When switching from IV to oral amiodarone, the dose depends on duration of IV therapy 5, 3:

IV <1 week: Start 800-1,600 mg oral daily 5, 3

IV 1-3 weeks: Start 600-800 mg oral daily 5, 3

IV >3 weeks: Start 400 mg oral daily 5, 3

These recommendations account for the 50% bioavailability of oral amiodarone and the significant tissue stores already accumulated during IV therapy 5, 3

Common Pitfalls to Avoid

  • Never use drop counter infusion sets (causes up to 30% underdosing) 3
  • Never infuse concentrations >2 mg/mL peripherally for >1 hour (severe phlebitis risk) 2, 3
  • Never administer faster than 30 mg/min initially (risk of hepatocellular necrosis) 3
  • Never give to patients with high-degree AV block without a pacemaker (can cause complete heart block) 2, 4
  • Do not drink grapefruit juice during oral amiodarone therapy (inhibits CYP3A metabolism) 3

Duration of Therapy

  • Infusions may be used after an episode of VT/VF but should be discontinued after 6-24 hours and the need for further arrhythmia management assessed 1
  • A maintenance infusion of up to 0.5 mg/min can be continued for 2-3 weeks regardless of age, renal function, or left ventricular function 3
  • There has been limited experience with IV amiodarone for longer than 3 weeks 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Amiodarone Infusion Protocol for Life-Threatening Ventricular Arrhythmias

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Amiodarone Administration Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Amiodarone Loading Dose 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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