The most commonly reported side effects of aceclidine include ocular hyperaemia, instillation site irritation, and visual impairment, based on 176 FDA adverse event reports from 2013 to 2025. 6.8% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for aceclidine.
These are voluntary reports and do not establish that aceclidine caused these reactions.
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Other drugs that appear in adverse event reports alongside aceclidine. 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.
56.3% of aceclidine adverse event reports involve female patients and 37.5% involve male patients. The largest age group is adult at 87%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking aceclidine when the adverse event was reported.
Aceclidine is sold under the brand name Vizz.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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