The most commonly reported side effects of glutethimide include autism spectrum disorder, foetal exposure during pregnancy, and overdose, based on 19 FDA adverse event reports from 2004 to 2023.
Percentages show how often each reaction appears relative to total reports for glutethimide.
These are voluntary reports and do not establish that glutethimide caused these reactions.
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Other drugs that appear in adverse event reports alongside glutethimide. 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.
57.9% of glutethimide adverse event reports involve female patients and 31.6% involve male patients. The largest age group is adult at 86%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking glutethimide when the adverse event was reported.
Glutethimide is sold under the brand name Doriden.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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