Amiodarone (IV — ICU/Peri-Arrest)
Brand names: Cordarone
Amiodarone is an antiarrhythmic used for serious atrial and ventricular arrhythmias, including peri-arrest and intensive-care settings, when other options are unsuitable.
Adult dose
Dose adjustments
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 UKDosage 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.
- NYHA Heart Failure Classification · Heart Failure
- Gupta Perioperative Risk for MI or Cardiac Arrest (MICA) · Perioperative Risk
- GO-FAR Score for Post-CPR Survival · Resuscitation
- CART Score for Cardiac Arrest Risk Triage · Resuscitation
- CAHP Cardiac Arrest Hospital Prognosis Score · Cardiac Arrest
- RESCUE-IHCA Score for ECPR in In-Hospital Cardiac Arrest · Cardiac Arrest