The most commonly reported side effects of histrelin include device breakage, procedural complication, and incorrect drug administration duration, based on 1,099 FDA adverse event reports from 2004 to 2025. 14.0% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for histrelin.
These are voluntary reports and do not establish that histrelin caused these reactions.
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Other drugs that appear in adverse event reports alongside histrelin. 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.
54.7% of histrelin adverse event reports involve female patients and 34.8% involve male patients. The largest age group is child at 68%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking histrelin when the adverse event was reported.
Showing 15 of 51 indications
Histrelin is sold under the brand name Vantas.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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