Neonatal Drug Therapy Manual

Amiodarone

Disclaimer: Official controlled document is the CHEO and Ottawa Hospital online copy. It is the responsibility of user to ensure that any paper copy version is the same as the online version before use.

Alternate Name(s): 
Cordarone
Classification: 
Antiarrhythmic Agent
Original Date: 
July 2003
Revised Date: 
Dec 2023
Indications: 
  • Supraventricular arrhythmias such as junctional ectopic tachycardia (JET), atrial flutter, atrial tachycardia
  • Management of resistant, life-threatening ventricular arrhythmias
Administration: 
  • IV loading dose over 60 minutes followed by a continuous infusion
  • IV direct, intraosseous: in cardiac arrest only
  • PO
Dosage: 
  • IV:
    • Stable Arrhythmias
      • Loading dose: 5 mg/kg/dose over 60 minutes followed by an infusion
      • Continuous infusion: 5 - 15 mcg/kg/min
      • Dilution concentration: 0.6 - 6 mg/mL (use central line if concentration > 2 mg/mL)
    •  Pulseless VF or VT
      • 5 mg/kg rapid IV bolus or intraosseous
  • PO:
    • Loading dose: 10 mg/kg/day as a single daily dose or divided BID for 7 to 10 days
    • Maintenance dose: 5 mg/kg/day as a single daily dose
Side Effects: 
  • CVS: bradycardia, heart block, hypertension (may be related to infusion rate)
  • Endocrine: hypothyroidism, hyperglycemia, increased triglycerides
  • Hematologic: coagulation abnormalities, thrombocytopenia
  • Hepatic: liver enzymes elevated, severe hepatic toxicity
  • Local: phlebitis (concentrations 2.5 mg/mL may be less irritating)
  • Ocular: corneal microdeposits, halos or blurred vision, photophobia, optic neuropathy, optic neuritis
  • Respiratory: intersitital pneumonitis, hypersensitivity pneumonitis
Parameters to Monitor: 
  • HR, BP
  • CXR
  • CBC, thyroid function tests, liver function tests
  • Ophthalmologic exams

 

Reconstitution and Stability: 
  • Amidarone 50 mg/mL
    • Add 0.4 mL (20 mg) of amiodarone to 19.6 mL of D5W
    • Final concentration: 1 mg/mL
  • Amiodarone 50 mg/mL
    • Add 0.8 mL (40 mg) of amiodarone to 19.2 mL of D5W
    • Final concentration: 2 mg/mL (central line only)
  • Stability: 24 hours at room temperature in IV syringes or glass bottles
Compatibility: 
  • Solutions Compatible: D5W
  • Y-site Compatible: amphotericin B, dobutamine, dopamine, epinephrine, fentanyl, gentamicin, midazolam, milrinone, morphine, vancomycin

Incompatible: SMOF, TPN

Notes: 

May increase serum digoxin levels - reduce digoxin dose by 50% during concurrent therapy

References: 

-Taketomo CK, Hodding JH, Kraus DM. Pediatric Dosage Handbook 9th-11th Editions. Hudson: Lexi-Comp Inc.; 2002-2004.

-Trissel LA. Handbook on Injectable Drugs. 12th-13th Editions. Bethesda: American Society of Health-System Pharmacists; 2003-2005.

-King JC. King Guide to Parenteral Admixtures. Internet Edition.

-The Children's Hospital of Eastern Ontario Parenteral Drug Manual. Department of Pharmacy 2003.

The information contained on this website is provided for informational purposes only, as a guide to assist physicians, nurses and other healthcare providers in deciding on the appropriate care required for a particular patient. At all times, physicians, nurses and other healthcare providers must exercise their independent clinical judgment, based on their knowledge, training and experience, taking into account the specific facts and circumstances of each patient, when deciding on the appropriate course of investigation and/or treatment to recommend in a particular clinical situation.

CHEO has made every effort to ensure that the information contained on this website is as current and accurate as possible. However, changes can occur due to ongoing research and the constant influx of new information. Where possible, hospitals and healthcare practitioners should verify the information before acting on it.

Reliance on any information in this website is at the user's own risk. CHEO is not responsible or liable for any harm, loss or other consequences from the use or misuse of the information on this website.