Abstract
BackgroundCefepime is a fourth-generation cephalosporin antibiotic used for the treatment of neutropenic fever, pneumonia, and urinary tract infections. The safety of cefepime is now being questioned as it has recently been implicated as a possible cause for lesser known adverse effects, including neurotoxicity. The objective of this study was to evaluate the association between cefepime and neurotoxicity.MethodsAdverse drug reactions (ADRs) reported to the U.S. Food and Drug Administration (FDA) from January 1, 2015 to September 30, 2017 were extracted from the FDA’s Adverse Event Reporting System (FAERS). The Medical Dictionary for Regulatory Activities (MedDRA) was used to identify preferred terms that were subsequently used to create a neurotoxicity composite ADR. Reporting Odds Ratios (RORs) and corresponding 95% confidence intervals (95% CI) were calculated for the neurotoxicity composite ADR and for common preferred terms associated with neurotoxicity. An association was considered to be statistically significant if the 95% CI did not include 1.0.ResultsThe neurotoxicity composite ADR (consisting of 40+ MedDRA preferred terms) occurred in 13.9% (n = 209/1504) of cefepime reports. Cefepime was three times more likely to have a report of the neurotoxicity composite ADR as compared with other drugs in the FDA’s FAERS database (ROR, 2.90; 95% CI, 2.51–3.36). The most frequent individual MedDRA preferred terms for the neurotoxicity composite ADR included (in descending order): “confusional state” (3.1%, 46/1,504), “mental status changes” (2.8%, 42/1,504), “encephalopathy” (2.3%, 35/1,504), “seizure” (2.3%, 34/1,504), “myoclonus” (1.8%, 27/1,504), and “neurotoxicity” (1.2%, 18/1,504). The highest RORs with cefepime vs. other drugs were (in descending order): “myoclonus” 45.0 (30.6–66.1), “encephalopathy” 29.7 (21.2–41.6), “mental status changes” 27.8 (20.4–37.8), “neurotoxicity” 26.7 (16.7–42.6), “confusional state” 4.3 (3.2–5.7), and “seizure” 3.5 (2.5–4.9).ConclusionCefepime was associated with significantly higher odds of myoclonus, encephalopathy, mental status changes, neurotoxicity, confusional state, seizure, and a neurotoxicity composite ADR as compared with other drugs. Practitioners should use caution in initiating cefepime in those patients at risk of neurotoxicity and monitor closely for ADRs.Disclosures All authors: No reported disclosures.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.