The most commonly reported side effects of repository include fatigue, weight increased, and malaise, based on 6,298 FDA adverse event reports from 2006 to 2025. 7.8% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for repository.
These are voluntary reports and do not establish that repository caused these reactions.
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Seriousness is determined by the reporter, not by OpenClaim.
Other drugs that appear in adverse event reports alongside repository. 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.
63.7% of repository adverse event reports involve female patients and 32.8% involve male patients. The largest age group is adult at 67%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking repository when the adverse event was reported.
Showing 15 of 324 indications
Repository is sold under the brand name H.p. Acthar Gel.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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