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1407. Disproportionality Analysis of Safety with Nafcillin and Oxacillin with the FDA Adverse Event Reporting System (FAERS)

BACKGROUND: Antistaphylococcal penicillins including oxacillin and nafcillin are among the drugs of choice for severe and invasive MSSA infections. While alternative agents such as cefazolin are associated with improved safety compared with antistaphylococcal penicillins, comparative safety data bet...

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Autores principales: Timbrook, Tristan T, Sutton, Jesse, Spivak, Emily
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254277/
http://dx.doi.org/10.1093/ofid/ofy210.1238
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author Timbrook, Tristan T
Sutton, Jesse
Spivak, Emily
author_facet Timbrook, Tristan T
Sutton, Jesse
Spivak, Emily
author_sort Timbrook, Tristan T
collection PubMed
description BACKGROUND: Antistaphylococcal penicillins including oxacillin and nafcillin are among the drugs of choice for severe and invasive MSSA infections. While alternative agents such as cefazolin are associated with improved safety compared with antistaphylococcal penicillins, comparative safety data between individual antistaphylococcal penicillins is limited and has shown possible improved safety with oxacillin among adults. The objective of this study was to determine the relative adverse events (AEs) reporting for these agents among the FDA Adverse Event Reporting System (FAERS) database. METHODS: We reviewed adverse events reports from the FAERS database from Q4/2003-Q1/2018 and performed a disproportionality analysis of safety events for nafcillin and oxacillin including ADEs related to acute kidney injury (AKI), rash, hypokalemia, and hepatotoxicity. Measures of association evaluated included reporting odds ratio (ROR) and proportion reporting ratio (PRR). RESULTS: Reports of AKI were substantially more common with nafcillin (PRR 23.2, 95% CI 18.4––29.3) than oxacillin (PRR 10.9, 95% CI 7.6––15.5). Rash was slightly higher with nafcillin than oxacillin (PRR 3.7, 95% CI 2.8––5.1 vs. 2.6, 95% CI 1.8––3.8). Hypokalemia was substantially more common with nafcillin than oxacillin (PRR 11.8, 95% CI 7.1––19.4 vs. 1.6, 95% CI 0.4––6.4). Hepatotoxcitiy was slightly higher reported among nafcillin than oxacillin (PRR 25.3, 95% CI 14.5––44.3 vs. 12.9, 95% CI 5.8––28.6). Similar observations were seen with RORs (Figure 1). CONCLUSION: Oxacillin may be associated with overall improved safety compared with nafcillin based on reporting signals from FAERS. Our results support previous limited observational data. With the likely equal efficacy of these agents, clinicians may want to consider prescribing oxacillin over nafcillin if an antistaphylococcal penicillin is indicated for an invasive MSSA infection. However, given the limitations of reporting systems, further evaluation is warranted. DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-62542772018-11-28 1407. Disproportionality Analysis of Safety with Nafcillin and Oxacillin with the FDA Adverse Event Reporting System (FAERS) Timbrook, Tristan T Sutton, Jesse Spivak, Emily Open Forum Infect Dis Abstracts BACKGROUND: Antistaphylococcal penicillins including oxacillin and nafcillin are among the drugs of choice for severe and invasive MSSA infections. While alternative agents such as cefazolin are associated with improved safety compared with antistaphylococcal penicillins, comparative safety data between individual antistaphylococcal penicillins is limited and has shown possible improved safety with oxacillin among adults. The objective of this study was to determine the relative adverse events (AEs) reporting for these agents among the FDA Adverse Event Reporting System (FAERS) database. METHODS: We reviewed adverse events reports from the FAERS database from Q4/2003-Q1/2018 and performed a disproportionality analysis of safety events for nafcillin and oxacillin including ADEs related to acute kidney injury (AKI), rash, hypokalemia, and hepatotoxicity. Measures of association evaluated included reporting odds ratio (ROR) and proportion reporting ratio (PRR). RESULTS: Reports of AKI were substantially more common with nafcillin (PRR 23.2, 95% CI 18.4––29.3) than oxacillin (PRR 10.9, 95% CI 7.6––15.5). Rash was slightly higher with nafcillin than oxacillin (PRR 3.7, 95% CI 2.8––5.1 vs. 2.6, 95% CI 1.8––3.8). Hypokalemia was substantially more common with nafcillin than oxacillin (PRR 11.8, 95% CI 7.1––19.4 vs. 1.6, 95% CI 0.4––6.4). Hepatotoxcitiy was slightly higher reported among nafcillin than oxacillin (PRR 25.3, 95% CI 14.5––44.3 vs. 12.9, 95% CI 5.8––28.6). Similar observations were seen with RORs (Figure 1). CONCLUSION: Oxacillin may be associated with overall improved safety compared with nafcillin based on reporting signals from FAERS. Our results support previous limited observational data. With the likely equal efficacy of these agents, clinicians may want to consider prescribing oxacillin over nafcillin if an antistaphylococcal penicillin is indicated for an invasive MSSA infection. However, given the limitations of reporting systems, further evaluation is warranted. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6254277/ http://dx.doi.org/10.1093/ofid/ofy210.1238 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Timbrook, Tristan T
Sutton, Jesse
Spivak, Emily
1407. Disproportionality Analysis of Safety with Nafcillin and Oxacillin with the FDA Adverse Event Reporting System (FAERS)
title 1407. Disproportionality Analysis of Safety with Nafcillin and Oxacillin with the FDA Adverse Event Reporting System (FAERS)
title_full 1407. Disproportionality Analysis of Safety with Nafcillin and Oxacillin with the FDA Adverse Event Reporting System (FAERS)
title_fullStr 1407. Disproportionality Analysis of Safety with Nafcillin and Oxacillin with the FDA Adverse Event Reporting System (FAERS)
title_full_unstemmed 1407. Disproportionality Analysis of Safety with Nafcillin and Oxacillin with the FDA Adverse Event Reporting System (FAERS)
title_short 1407. Disproportionality Analysis of Safety with Nafcillin and Oxacillin with the FDA Adverse Event Reporting System (FAERS)
title_sort 1407. disproportionality analysis of safety with nafcillin and oxacillin with the fda adverse event reporting system (faers)
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254277/
http://dx.doi.org/10.1093/ofid/ofy210.1238
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