The most commonly reported side effects of omidenepag include cataract, anaphylactic reaction, and macular oedema, based on 52 FDA adverse event reports from 2023 to 2025.
Percentages show how often each reaction appears relative to total reports for omidenepag.
These are voluntary reports and do not establish that omidenepag caused these reactions.
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Seriousness is determined by the reporter, not by OpenClaim.
Other drugs that appear in adverse event reports alongside omidenepag. 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.
71.2% of omidenepag adverse event reports involve female patients and 23.1% involve male patients. The largest age group is elderly at 64%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking omidenepag when the adverse event was reported.
Omidenepag is sold under the brand name Omlonti.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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