The most commonly reported side effects of glatiramer include injection site pain, multiple sclerosis relapse, and injection site reaction, based on 62,243 FDA adverse event reports from 2004 to 2025. 6.5% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for glatiramer.
These are voluntary reports and do not establish that glatiramer caused these reactions.
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Other drugs that appear in adverse event reports alongside glatiramer. 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.
76.0% of glatiramer adverse event reports involve female patients and 18.5% involve male patients. The largest age group is adult at 87%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking glatiramer when the adverse event was reported.
Showing 15 of 211 indications
Glatiramer is sold under the brand name Copaxone.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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