The most commonly reported side effects of echothiophate include intraocular pressure increased, visual impairment, and eye pain, based on 166 FDA adverse event reports from 2005 to 2025. 10.2% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for echothiophate.
These are voluntary reports and do not establish that echothiophate caused these reactions.
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Other drugs that appear in adverse event reports alongside echothiophate. 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.
56.0% of echothiophate adverse event reports involve female patients and 36.1% involve male patients. The largest age group is elderly at 57%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking echothiophate when the adverse event was reported.
Showing 15 of 27 indications
Echothiophate is sold under the brand name Phospholine Iodide.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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