The most commonly reported side effects of iotrolan include posterior reversible encephalopathy syndrome, dizziness, and anterior spinal artery syndrome, based on 8 FDA adverse event reports from 2004 to 2021.
Percentages show how often each reaction appears relative to total reports for iotrolan.
These are voluntary reports and do not establish that iotrolan caused these reactions.
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Other drugs that appear in adverse event reports alongside iotrolan. 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.
87.5% of iotrolan adverse event reports involve female patients and 12.5% involve male patients. The largest age group is adult at 86%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking iotrolan when the adverse event was reported.
Iotrolan is sold under the brand name Osmovist 190.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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