Cordarone (Amiodarone) Intravenous Dosing
For life-threatening ventricular arrhythmias or hemodynamically stable wide-complex tachycardia, administer a 150 mg IV bolus over 10 minutes, followed by 1 mg/min infusion for 6 hours, then 0.5 mg/min for 18 hours, delivering approximately 1 gram in the first 24 hours. 1
Standard IV Dosing Protocol
Rapid Loading Phase
- Initial bolus: 150 mg diluted in 100 mL of 5% dextrose (D5W) administered over 10 minutes 1
- This bolus may be repeated after 10-30 minutes if breakthrough arrhythmias occur 2
- For cardiac arrest or immediately life-threatening situations, the 150 mg bolus can be given over 10-15 minutes and repeated after 1 hour if needed 1
Maintenance Infusion
- Early maintenance: 1 mg/min for 6 hours (delivers approximately 360 mg) 2, 1
- Late maintenance: 0.5 mg/min for the remaining 18 hours (delivers approximately 540 mg) 2, 1
- Total 24-hour dose: Approximately 1000 mg from combined bolus and infusions 1
- Maximum cumulative dose: Do not exceed 2.2 grams within any 24-hour period 1
Administration Requirements
- Must use 5% dextrose in water (D5W) as the diluent; normal saline or lactated Ringer's causes precipitation 1
- Concentration should not exceed 2 mg/mL unless administered through a central venous catheter 1
- Use a central line whenever possible, as peripheral vein phlebitis occurs frequently with concentrations >2 mg/mL 1
- Use an in-line filter during administration 1
Onset of Action and Clinical Expectations
The antiarrhythmic effect typically becomes apparent 20-30 minutes after IV administration 2, 1. However, most conversions to sinus rhythm occur after 6-8 hours and often require at least 1 gram total dose 1. This delayed onset makes amiodarone less appropriate as a first-line agent unless the patient is clinically stable 1.
Critical Monitoring Requirements
Continuous Monitoring Mandatory
- ECG monitoring: Heart rate, AV conduction abnormalities, PR interval, QRS duration, and QT prolongation 1
- Blood pressure: Hypotension occurs in 16-26% of patients receiving IV amiodarone 1
- Heart rate: Bradycardia develops in 4.9% of patients, regardless of dose 1
When to Reduce or Stop Infusion
- If bradycardia or heart block develops, discontinue the infusion or reduce the rate immediately 1
- If heart rate decreases by 10 beats per minute, reduce the infusion rate 1
- Monitor for second- or third-degree heart block, which represents an absolute contraindication to continued therapy without pacemaker support 1
Relative Contraindications Requiring Extreme Caution
IV amiodarone should be used with extreme caution and is relatively contraindicated in the following situations unless the arrhythmia is immediately life-threatening and no safer alternatives exist: 1
- Baseline heart rate <60 bpm (especially <57 bpm) 1
- Systolic blood pressure <100 mmHg 1
- Moderate or severe left ventricular dysfunction 1
- Second- or third-degree heart block without a pacemaker 1
High-Risk Drug Interactions
- Concomitant rate-control medications (beta-blockers, calcium channel blockers, digoxin) create additive effects and significantly increase bradycardia risk 1
- Reduce digoxin dose by 50% when starting amiodarone, as digoxin levels predictably double 1, 3
- Reduce warfarin dose by one-third to one-half and monitor INR at least weekly for the first 6 weeks, as interaction effects don't peak until 7 weeks 1, 3
Alternative Agents for Hemodynamically Stable Wide-Complex Tachycardia
Given amiodarone's delayed onset and potential for hypotension/bradycardia, consider these alternatives first in stable patients: 1
- Procainamide: 20-50 mg/min until arrhythmia suppression, hypotension develops, QRS widens by ≥50%, or cumulative dose of 17 mg/kg is reached 1
- Lidocaine: Initial IV dose of 1-1.5 mg/kg when amiodarone is unavailable 1
- Beta-blockers or calcium channel blockers may be better tolerated for rate control 1
Electrical Cardioversion Priority
If the patient becomes hemodynamically unstable at any point during pharmacologic therapy, immediate electrical cardioversion should be prioritized over continued drug administration. 1
Transitioning to Oral Therapy
When converting from IV to oral amiodarone, base the oral dose on duration of IV therapy: 4
- IV therapy <1 week: 800-1,600 mg oral daily 4
- IV therapy 1-3 weeks: 600-800 mg oral daily 4
- IV therapy >3 weeks: 400 mg oral daily 4
The extremely long half-life (average 58 days, range 15-100 days) creates significant overlap between IV and oral dosing 1, 3.
Common Pitfalls to Avoid
- Do not use normal saline or lactated Ringer's as diluent—only D5W 1
- Do not exceed 2 mg/mL concentration in peripheral lines 1
- Do not forget to adjust digoxin and warfarin doses when initiating amiodarone 1, 3
- Do not administer to patients with baseline bradycardia unless pacemaker is in place or situation is immediately life-threatening 1
- Patients must not consume grapefruit or grapefruit juice during therapy, as it inhibits CYP3A-mediated metabolism and increases plasma levels 1