The most commonly reported side effects of cephapirin include chest discomfort, dyspnoea, and condition aggravated, based on 37 FDA adverse event reports from 2004 to 2024. 5.4% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for cephapirin.
These are voluntary reports and do not establish that cephapirin caused these reactions.
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Other drugs that appear in adverse event reports alongside cephapirin. 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.
32.4% of cephapirin adverse event reports involve female patients and 64.9% involve male patients. The largest age group is elderly at 52%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking cephapirin when the adverse event was reported.
Cephapirin is sold under the brand name Cephapirin Sodium.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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