The most commonly reported side effects of iothalamate include incorrect route of drug administration, incorrect route of drug administration, and dyspnoea, based on 120 FDA adverse event reports from 2004 to 2025.
Percentages show how often each reaction appears relative to total reports for iothalamate.
These are voluntary reports and do not establish that iothalamate caused these reactions.
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Other drugs that appear in adverse event reports alongside iothalamate. 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.
35.8% of iothalamate adverse event reports involve female patients and 33.3% involve male patients. The largest age group is adult at 70%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking iothalamate when the adverse event was reported.
Showing 15 of 39 indications
Iothalamate is sold under brand names including Glofil-125, Conray 30, Conray 325.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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