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Antiarrhythmic (Class III) Pregnancy: Contraindicated in pregnancy except in exceptional circumstances. Amiodarone and N-desmethylamiodarone cross the placenta, achieving 10-25% of maternal plasma concentrations in the infant; hypothyroidism, bradycardia and prolonged QT intervals were observed in approximately 10% of newborns, with impaired growth and preterm birth also reported. Given the long half-life, women of child-bearing age would need to plan a pregnancy starting at least half a year after finishing therapy. Breast-feeding should be stopped if therapy is required.

Amiodarone (IV — ICU/Peri-Arrest)

Brand names: Cordarone

Used in: Atrial Fibrillation

Amiodarone is an antiarrhythmic used for serious atrial and ventricular arrhythmias, including peri-arrest and intensive-care settings, when other options are unsuitable.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: Loading dose 5 mg/kg bodyweight by intravenous infusion over a period of 20 minutes to 2 hours, as a dilute solution in 250 ml 5% dextrose
Route: Intravenous infusion via a central venous route; the peripheral venous route may be used for cardiopulmonary resuscitation in cardiac arrest related to ventricular fibrillation resistant to defibrillation
Frequency: Loading infusion over 20 minutes to 2 hours, then followed by a maintenance infusion; infusion rate adjusted on the basis of clinical response
Max: Loading may be followed by repeat infusion up to 1200 mg (approximately 15 mg/kg bodyweight) in up to 500 ml 5% dextrose per 24 hours. Maintenance maximum 1200 mg per 24 hours (maximum 8 ampoules). For direct injection the proposed dose of 5 mg/kg must not be exceeded.
Source quote (eMC §4.2): 'The standard recommended dose is 5mg/kg bodyweight given by intravenous infusion over a period of 20 minutes to 2 hours.' Amiodarone should only be used where facilities exist for cardiac monitoring, defibrillation and cardiac pacing, and only in a special care unit under continuous ECG and blood pressure monitoring. MAINTENANCE INFUSION: 10-20 mg per kg bodyweight in physiological glucose solution every 24 hours (on average 600 to 800 mg per 24 hours, up to a maximum of 1200 mg per 24 hours) for a few days. EXTREME CLINICAL EMERGENCY (slow injection): at the discretion of the clinician, 150-300 mg (or 2.5-5 mg/kg) in 10-20 ml 5% glucose over a minimum of 3 minutes; this should not be repeated for at least 15 minutes, and patients treated this way must be closely monitored, e.g. in an intensive care unit. CARDIOPULMONARY RESUSCITATION: the recommended dose for ventricular fibrillation / pulseless ventricular tachycardia resistant to defibrillation is 300 mg (or 5 mg/kg bodyweight) diluted in 20 ml 5% dextrose and rapidly injected; an additional 150 mg (or 2.5 mg/kg bodyweight) IV dose may be considered if ventricular fibrillation persists. For prolonged, refractory ventricular fibrillation after adrenaline and defibrillation: 300 mg as bolus injection, repeated if necessary with a 150 mg bolus injection. Amiodarone can cause severe irritation of the vein — adequate rinsing after bolus injection must be ensured, and peripheral administration should be followed by 200 ml of infusion fluid. DILUTION LIMITS: do not use concentrations below 300 mg per 500 ml; to prevent phlebitis do not use concentrations exceeding 3 mg/ml; do not add other medicinal products to the infusion fluid and do not give other substances in the same syringe. A central line is recommended whenever repeated or continuous infusions are intended. CHANGEOVER TO ORAL: as soon as an adequate response has been obtained (if possible commence oral maintenance on the first day of the infusion), oral therapy should be initiated concomitantly at the usual loading dose (200 mg three times a day), then phased out gradually. STATINS: in patients taking amiodarone with simvastatin, the simvastatin dose should not exceed 20 mg/day. ELDERLY: use the minimum effective dose; the elderly may be more susceptible to bradycardia and conduction defects if too high a dose is employed; pay particular attention to thyroid function monitoring. PAEDIATRIC: safety and efficacy in children have not been established, and because of the benzyl alcohol content intravenous amiodarone is CONTRAINDICATED in neonates, infants and children up to 3 years old — verify any paediatric use against a children's formulary.

Dose adjustments

Renal

eMC §4.2 states that although no dosage adjustment for patients with kidney or liver abnormalities has been defined during chronic treatment with oral amiodarone, close clinical monitoring is prudent for elderly patients.

Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.

US labelling (FDA)

Reference — US labelling, may differ from UK

Dosage must be individualized based on severity of arrhythmia and response. Use the lowest effective dose. Obtain baseline chest x-ray, pulmonary function tests, thyroid function tests, and liver aminotransferases. Correct hypokalemia, hypomagnesemia, and hypocalcemia before initiating treatment. Initiate treatment with a loading dose of 800 to 1600 mg/day until initial therapeutic response occurs (usually 1 to 3 weeks). Once adequate arrhythmia control is achieved, or if side effects become prominent, reduce Pacerone tablets dose to 600 to 800 mg/day for one month and then to the maintenance dose, usually 400 mg/day. ( 2 ) Recommended Dosage: Initiate treatment with a loading dose of 800 …

Source: US FDA prescribing information (openFDA / DailyMed), label dated 2024-02-02. Accessed 2026-06-12. US dosing and indications can differ from UK practice — use UK sources for prescribing decisions.

Contraindications

  • Known hypersensitivity to iodine or to amiodarone, or to any of the excipients (one ampoule contains approximately 56 mg iodine)
  • Sinus bradycardia, sino-atrial heart block; in severe conduction disturbances (high grade AV block, bifascicular or trifascicular block) or sinus node disease, use only in conjunction with a pacemaker
  • Combination with drugs which may induce torsades de pointes
  • Severe respiratory failure, circulatory collapse or severe arterial hypotension; hypotension, heart failure and cardiomyopathy are also contraindications when amiodarone is used as a bolus injection
  • Evidence or history of thyroid dysfunction (thyroid function tests should be performed where appropriate prior to therapy)
  • Neonates, infants and children up to 3 years old (presence of benzyl alcohol)
  • Pregnancy, except in exceptional circumstances; lactation (allowed only in special life-threatening circumstances)
  • The SPC notes that not all of the above contraindications apply to the use of amiodarone for cardiopulmonary resuscitation of shock-resistant ventricular fibrillation

Side effects

  • Injection site reactions — pain, erythema, oedema, necrosis, extravasation, inflammation, induration, thrombophlebitis, phlebitis, cellulitis (common)
  • Bradycardia, generally moderate (common); very rarely marked bradycardia or sinus arrest requiring discontinuation, especially with sinus node dysfunction or in elderly patients
  • Hypothyroidism, and hyperthyroidism which is sometimes fatal (common)
  • Corneal micro-deposits at the anterior surface of the cornea, found in almost every patient; may cause coloured halos in dazzling light or blurred vision, usually regressing 6-12 months after discontinuation (very common)
  • Extrapyramidal tremor (common), usually regressing after dose reduction or withdrawal
  • Onset or worsening of arrhythmia, sometimes followed by cardiac arrest (very rare); torsades de pointes (frequency not known)

Interactions

  • Drugs which may induce torsades de pointes — combination is contraindicated (eMC §4.3)
  • Simvastatin — increased risk of myopathy/rhabdomyolysis; the simvastatin dose should not exceed 20 mg/day and other statins should be used at low dosage (eMC §4.4)
  • QT-prolonging drugs — class I and III antiarrhythmics, lithium, certain phenothiazines, tricyclic antidepressants, certain fluoroquinolone and macrolide antibiotics, azole antifungals, halogenated inhalation anaesthetic agents: increased risk of torsade de pointes; avoid concomitant use (US label §7)
  • Negative chronotropes — digoxin, beta blockers, verapamil, diltiazem, clonidine, ivabradine: bradycardia, sinus arrest and AV block; monitor heart rate (US label §7)
  • CYP450 inhibitors — grapefruit juice, certain fluoroquinolone and macrolide antibiotics, azole antifungals, cimetidine, certain protease inhibitors: increased amiodarone exposure; avoid concomitant use (US label §7)
  • Ciclosporin — increased plasma ciclosporin levels with elevated creatinine despite dose reduction; monitor levels and renal function (US label §7)
  • NOTE: the fetched eMC bundle did not include §4.5, so entries marked 'US label' come from US prescribing information and must be checked against the UK SPC §4.5

Clinical monograph

How it works

A predominantly class III antiarrhythmic (potassium-channel blockade prolonging repolarisation) with additional sodium, calcium and beta-blocking effects, slowing conduction and prolonging refractoriness.

Prescribing in practice

  • It has a very long half-life and extensive tissue accumulation, so effects and interactions persist for weeks after stopping.
  • Serious organ toxicities occur with longer use — thyroid (over- and under-active), pulmonary fibrosis, hepatotoxicity, corneal deposits, photosensitivity and skin discolouration.
  • Major interactions include warfarin and digoxin (reduce their doses) and other QT-prolonging drugs; give intravenous amiodarone via a central line where possible.

Monitoring

Baseline and periodic thyroid and liver function and a chest X-ray; review for visual, pulmonary or skin effects; monitor ECG (QT) and interacting-drug levels (INR, digoxin).

Counselling the patient

  • Use sun protection — it can make you burn easily and can discolour the skin.
  • Report breathlessness or cough, or symptoms of thyroid problems.
  • Mention it to clinicians for a long time after stopping, as it lingers and interacts.

Evidence & guidelines

Used for serious arrhythmias including peri-arrest (Resuscitation Council UK), reserved because of its toxicity profile.

Reference: Resuscitation Council UK ALS 2021; MHRA Amiodarone Safety Update; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.