The most commonly reported side effects of loracarbef include drug hypersensitivity, anaphylactic shock, and acute kidney injury, based on 86 FDA adverse event reports from 2004 to 2023.
Percentages show how often each reaction appears relative to total reports for loracarbef.
These are voluntary reports and do not establish that loracarbef caused these reactions.
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Other drugs that appear in adverse event reports alongside loracarbef. 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.
67.4% of loracarbef adverse event reports involve female patients and 22.1% involve male patients. The largest age group is adult at 68%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking loracarbef when the adverse event was reported.
Showing 15 of 22 indications
Loracarbef is sold under the brand name Lorabid.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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