The most commonly reported side effects of miglitol include hepatic function abnormal, blood glucose increased, and liver disorder, based on 1,309 FDA adverse event reports from 2004 to 2025.
Percentages show how often each reaction appears relative to total reports for miglitol.
These are voluntary reports and do not establish that miglitol caused these reactions.
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Other drugs that appear in adverse event reports alongside miglitol. 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.
38.6% of miglitol adverse event reports involve female patients and 53.5% involve male patients. The largest age group is elderly at 62%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking miglitol when the adverse event was reported.
Showing 15 of 50 indications
Miglitol is sold under the brand name Miglitol.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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