The most commonly reported side effects of suprofen include cardiac arrest, off label use, and acute kidney injury, based on 47 FDA adverse event reports from 2005 to 2025.
Percentages show how often each reaction appears relative to total reports for suprofen.
These are voluntary reports and do not establish that suprofen caused these reactions.
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Seriousness is determined by the reporter, not by OpenClaim.
Other drugs that appear in adverse event reports alongside suprofen. 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.
46.8% of suprofen adverse event reports involve female patients and 40.4% involve male patients. The largest age group is adult at 44%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking suprofen when the adverse event was reported.
Suprofen is sold under the brand name Profenal.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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