The most commonly reported side effects of deserpidine include fatigue, dry mouth, and middle insomnia, based on 26 FDA adverse event reports from 2004 to 2024.
Percentages show how often each reaction appears relative to total reports for deserpidine.
These are voluntary reports and do not establish that deserpidine caused these reactions.
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Other drugs that appear in adverse event reports alongside deserpidine. 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.
65.4% of deserpidine adverse event reports involve female patients and 26.9% involve male patients. The largest age group is elderly at 67%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking deserpidine when the adverse event was reported.
Deserpidine is sold under the brand name Oreticyl Forte.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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