The most commonly reported side effects of dexchlorpheniramine include pyrexia, off label use, and dyspnoea, based on 10,853 FDA adverse event reports from 2004 to 2025.
Percentages show how often each reaction appears relative to total reports for dexchlorpheniramine.
These are voluntary reports and do not establish that dexchlorpheniramine caused these reactions.
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Other drugs that appear in adverse event reports alongside dexchlorpheniramine. 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.
47.3% of dexchlorpheniramine adverse event reports involve female patients and 45.4% involve male patients. The largest age group is adult at 47%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking dexchlorpheniramine when the adverse event was reported.
Showing 15 of 377 indications
Dexchlorpheniramine is sold under the brand name Dexchlorpheniramine Maleate.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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