The most commonly reported side effects of dydrogesterone include maternal exposure during pregnancy, exposure during pregnancy, and off label use, based on 241 FDA adverse event reports from 2004 to 2025.
Percentages show how often each reaction appears relative to total reports for dydrogesterone.
These are voluntary reports and do not establish that dydrogesterone caused these reactions.
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Other drugs that appear in adverse event reports alongside dydrogesterone. 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.
83.8% of dydrogesterone adverse event reports involve female patients and 6.2% involve male patients. The largest age group is adult at 84%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking dydrogesterone when the adverse event was reported.
Showing 15 of 72 indications
Dydrogesterone is sold under the brand name Gynorest.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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