The most commonly reported side effects of bacampicillin include type iv hypersensitivity reaction, therapeutic product cross-reactivity, and rash maculo-papular, based on 30 FDA adverse event reports from 2005 to 2022.
Percentages show how often each reaction appears relative to total reports for bacampicillin.
These are voluntary reports and do not establish that bacampicillin caused these reactions.
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Other drugs that appear in adverse event reports alongside bacampicillin. 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.
66.7% of bacampicillin adverse event reports involve female patients and 33.3% involve male patients. The largest age group is adult at 74%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking bacampicillin when the adverse event was reported.
Bacampicillin is sold under the brand name Spectrobid.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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