The most commonly reported side effects of ceftazidime include off label use, pyrexia, and acute kidney injury, based on 9,152 FDA adverse event reports from 2004 to 2025. 9.5% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for ceftazidime.
These are voluntary reports and do not establish that ceftazidime caused these reactions.
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Other drugs that appear in adverse event reports alongside ceftazidime. 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.
39.7% of ceftazidime adverse event reports involve female patients and 50.5% involve male patients. The largest age group is adult at 45%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking ceftazidime when the adverse event was reported.
Showing 15 of 755 indications
Ceftazidime is sold under brand names including Tazidime In Plastic Container, Ceftazidime Sodium In Plastic Container.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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