The most commonly reported side effects of retapamulin include application site irritation, burning sensation, and application site pain, based on 718 FDA adverse event reports from 2007 to 2023. 7.5% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for retapamulin.
These are voluntary reports and do not establish that retapamulin caused these reactions.
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Other drugs that appear in adverse event reports alongside retapamulin. 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.
44.6% of retapamulin adverse event reports involve female patients and 25.2% 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 retapamulin when the adverse event was reported.
Showing 15 of 78 indications
Retapamulin is sold under the brand name Altabax.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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