The most commonly reported side effects of dinoprost include foetal exposure during pregnancy, respiratory failure, and drug withdrawal syndrome neonatal, based on 32 FDA adverse event reports from 2004 to 2024.
Percentages show how often each reaction appears relative to total reports for dinoprost.
These are voluntary reports and do not establish that dinoprost caused these reactions.
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Other drugs that appear in adverse event reports alongside dinoprost. 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.
34.4% of dinoprost adverse event reports involve female patients and 56.3% involve male patients. The largest age group is adult at 54%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking dinoprost when the adverse event was reported.
Dinoprost is sold under the brand name Prostin F2 Alpha.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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