The most commonly reported side effects of iodine include skin irritation, thermal burn, and blister, based on 185 FDA adverse event reports from 2004 to 2025.
Percentages show how often each reaction appears relative to total reports for iodine.
These are voluntary reports and do not establish that iodine caused these reactions.
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Other drugs that appear in adverse event reports alongside iodine. Drugs flagged as a suspected cause appear in the first column. Drugs taken at the same time but not suspected appear in the second.
Also suspected
Taken alongside
Co-occurrence in adverse event reports does not establish a drug interaction. Patients often take multiple medications, and these lists reflect prescribing patterns rather than causal relationships. Consult a healthcare provider about potential drug interactions.
44.9% of iodine adverse event reports involve female patients and 26.5% involve male patients. The largest age group is adult at 67%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking iodine when the adverse event was reported.
Iodine is sold under the brand name Duraprep.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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