The most commonly reported side effects of hexaminolevulinate include pain, medication error, and micturition urgency, based on 45 FDA adverse event reports from 2011 to 2025. 20.0% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for hexaminolevulinate.
These are voluntary reports and do not establish that hexaminolevulinate caused these reactions.
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Other drugs that appear in adverse event reports alongside hexaminolevulinate. 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.
17.8% of hexaminolevulinate adverse event reports involve female patients and 20.0% involve male patients. The largest age group is elderly at 93%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking hexaminolevulinate when the adverse event was reported.
Hexaminolevulinate is sold under the brand name Cysview Kit.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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