R. Michael Morse, MD; Gregg A. Valenzuela, MD; Todd P. Greenwald, MD; Philip J. Eulie, MD; Robert C. Wesley, MD; Richard W. McCallum, MD
Amiodarone, a benzofuran derivative structurally related to thyroxine, has been used to treat heart disease for 25 years. It is an amphophilic compound that may induce secondary phospholipidosis. It can produce adverse events in up to 74% of patients at 1 year and 94% of patients at 3 years (1, 2) in a log linear relation to the total dose or duration of therapy. Reported side effects include corneal microdeposits, renal dysfunction, hypertriglyceridemia, nausea and vomiting, and photodermatitis; mental symptoms, such as fatigue, paresthesias, and sleep disturbances, have also been described. Toxic effects include increased atrioventricular or intraventricular conduction delay,
R. Michael Morse, Gregg A. Valenzuela, Todd P. Greenwald, Philip J. Eulie, Robert C. Wesley, Richard W. McCallum. Amiodarone-Induced Liver Toxicity. Ann Intern Med. 1988;109:838–840. doi: 10.7326/0003-4819-109-10-838
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Published: Ann Intern Med. 1988;109(10):838-840.
Cardiology, Emergency Medicine, Gastroenterology/Hepatology, Liver Disease, Rhythm Disorders and Devices.
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