The most commonly reported side effects of ponesimod include product dose omission issue, fatigue, and dyspnoea, based on 322 FDA adverse event reports from 2020 to 2025. 3.1% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for ponesimod.
These are voluntary reports and do not establish that ponesimod caused these reactions.
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Other drugs that appear in adverse event reports alongside ponesimod. 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.
62.4% of ponesimod adverse event reports involve female patients and 17.4% involve male patients. The largest age group is adult at 95%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking ponesimod when the adverse event was reported.
Ponesimod is sold under the brand name Ponvory.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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