The most commonly reported side effects of ertugliflozin include nausea, product dose omission issue, and vomiting, based on 1,249 FDA adverse event reports from 2013 to 2025. 3.9% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for ertugliflozin.
These are voluntary reports and do not establish that ertugliflozin caused these reactions.
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Other drugs that appear in adverse event reports alongside ertugliflozin. 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.
49.3% of ertugliflozin adverse event reports involve female patients and 45.2% involve male patients. The largest age group is adult at 68%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking ertugliflozin when the adverse event was reported.
Showing 15 of 43 indications
Ertugliflozin is sold under the brand name Segluromet.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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