The most commonly reported side effects of trypan include toxic anterior segment syndrome, blindness, and corneal oedema, based on 50 FDA adverse event reports from 2010 to 2025.
Percentages show how often each reaction appears relative to total reports for trypan.
These are voluntary reports and do not establish that trypan caused these reactions.
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Other drugs that appear in adverse event reports alongside trypan. 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.
34.0% of trypan adverse event reports involve female patients and 54.0% 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 trypan when the adverse event was reported.
Trypan is sold under the brand name Membraneblue.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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