The most commonly reported side effects of memantine include death, fall, and off label use, based on 27,915 FDA adverse event reports from 2004 to 2025. 4.7% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for memantine.
These are voluntary reports and do not establish that memantine caused these reactions.
Report severity
Seriousness is determined by the reporter, not by OpenClaim.
Other drugs that appear in adverse event reports alongside memantine. 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.
50.5% of memantine adverse event reports involve female patients and 41.7% involve male patients. The largest age group is elderly at 83%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking memantine when the adverse event was reported.
Showing 15 of 475 indications
Memantine is sold under the brand name Memantine Hydrochloride And Donepezil Hydrochloride.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
Ask OpenClaim about your specific drug combination. Get a sourced report using FDA data, drug labels, and medical literature.