The most commonly reported side effects of benoxinate include toxic anterior segment syndrome, aqueous fibrin, and inflammation, based on 164 FDA adverse event reports from 2004 to 2025.
Percentages show how often each reaction appears relative to total reports for benoxinate.
These are voluntary reports and do not establish that benoxinate caused these reactions.
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Other drugs that appear in adverse event reports alongside benoxinate. 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.
43.3% of benoxinate adverse event reports involve female patients and 26.2% involve male patients. The largest age group is elderly at 60%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking benoxinate when the adverse event was reported.
Showing 15 of 33 indications
Benoxinate is sold under the brand name Fluorescein Sodium And Benoxinate Hydrochloride.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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