
The most commonly reported side effects of ethiodized include off label use, product use in unapproved indication, and liver abscess, based on 1,522 FDA adverse event reports from 2004 to 2025.
Percentages show how often each reaction appears relative to total reports for ethiodized.
These are voluntary reports and do not establish that ethiodized caused these reactions.
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Other drugs that appear in adverse event reports alongside ethiodized. 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.
28.6% of ethiodized adverse event reports involve female patients and 54.3% involve male patients. The largest age group is adult at 51%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking ethiodized when the adverse event was reported.
Showing 15 of 131 indications
Ethiodized is sold under the brand name Lipiodol.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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