The most commonly reported side effects of iodipamide include depression, dry mouth, and duodenal ulcer perforation, based on 34 FDA adverse event reports from 2005 to 2025.
Percentages show how often each reaction appears relative to total reports for iodipamide.
These are voluntary reports and do not establish that iodipamide caused these reactions.
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Other drugs that appear in adverse event reports alongside iodipamide. 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.
67.6% of iodipamide adverse event reports involve female patients and 14.7% involve male patients. The largest age group is adult at 93%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking iodipamide when the adverse event was reported.
Iodipamide is sold under the brand name Cholografin Meglumine.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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