| Standard dosage | Initial load of 800–1600 mg/day for 1–3 weeks, followed by 200–600 mg/day |
| Contraindications | Significant bradycardia, pregnancy or breastfeeding, baseline pulmonary disease, baseline hepatic impairment, baseline thyroid disease |
| Main drug interactions | Drugs which are metabolized by CYP enzymes including warfarin (amiodarone is a potent inhibitor of CYP enzymes) and drugs which prolong the QT interval |
| Main side effects | Chronic interstitial pneumonitis, hyper- and hypothyroidism, hepatitis, corneal microdeposits, photosensitivity, skin discoloration, GI upset, QT prolongation and ventricular arrhythmias |
| Special points | Primarily a Class III agent (potassium channel blocker) but crosses all four classes. |
| Considered the most effective AAD. | |
| Has the least cardiac toxicity but the most extra-cardiac toxicity. | |
| Generally safe in heart failure, structural heart disease, and coronary artery disease. | |
| Monitoring recommendations include thyroid function tests every 6 months, liver function tests every 6 months, eye examination yearly, pulmonary function tests/chest x-ray yearly. | |
| Cost/cost-effectiveness | Generic (approximate cost $36 per month). Can be initiated on an outpatient basis. |