The most commonly reported side effects of cefonicid include platelet count decreased, pyrexia, and white blood cell count decreased, based on 43 FDA adverse event reports from 2005 to 2024. 4.7% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for cefonicid.
These are voluntary reports and do not establish that cefonicid caused these reactions.
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Other drugs that appear in adverse event reports alongside cefonicid. 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.
51.2% of cefonicid adverse event reports involve female patients and 46.5% involve male patients. The largest age group is adult at 51%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking cefonicid when the adverse event was reported.
Showing 15 of 19 indications
Cefonicid is sold under the brand name Monocid.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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