The most commonly reported side effects of gadobenate include nephrogenic systemic fibrosis, pain, and nausea, based on 4,338 FDA adverse event reports from 2005 to 2025.
Percentages show how often each reaction appears relative to total reports for gadobenate.
These are voluntary reports and do not establish that gadobenate caused these reactions.
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Other drugs that appear in adverse event reports alongside gadobenate. 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.
54.8% of gadobenate adverse event reports involve female patients and 36.2% involve male patients. The largest age group is adult at 73%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking gadobenate when the adverse event was reported.
Showing 15 of 444 indications
Gadobenate is sold under the brand name Multihance Multipack.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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