The most commonly reported side effects of gepotidacin include small for dates baby, neonatal respiratory distress syndrome, and hyperbilirubinaemia neonatal, based on 14 FDA adverse event reports from 2012 to 2025.
Percentages show how often each reaction appears relative to total reports for gepotidacin.
These are voluntary reports and do not establish that gepotidacin caused these reactions.
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Other drugs that appear in adverse event reports alongside gepotidacin. 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.
28.6% of gepotidacin adverse event reports involve female patients and 64.3% involve male patients. The largest age group is adult at 42%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking gepotidacin when the adverse event was reported.
Gepotidacin is sold under the brand name Blujepa.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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