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551. A Multistate Investigation of Serious Adverse Events, Including Deaths, Following Ceftriaxone Injections, September 2024–June 2025

Title: 551. A Multistate Investigation of Serious Adverse Events, Including Deaths, Following Ceftriaxone Injections, September 2024–June 2025
Authors: Pierce, Rebecca; Agarwal, Radhika; Kayira, Dumbani; Lyles, Jennifer Lind; Sivilus, Maribeth; Morrison, Melissa A; Stubblefield, Andrew W; Roderick, Melanie; Landers, Karen; Harris, Scott; Dulski, Theresa; Garner, Kelley; Bhattarai, Rachana; Stoltey, Juliet; Biehle, Lauren; Czaja, Christopher A; Hoffner, Joshua T; Charles, Argentina; Wagner, JoAnna; Gulley, Trent; Beeman, Haley; Thoroughman, Douglas A; Curran, Michael J; Flinchum, Andrea H; Salinas, Andrea; Lee, Grace; Moore, Riley; Brennan, Brenda M; Patel, Gargi; Mehr, Jason; Tran, Dat; Breitenstein, Liz; Sinkevitch, Jenna N; Tressler, Stacy; Kinsey, Cara Bicking; Tori, Marco; Wilson, Christopher; Godwin, Simone; Miller, Malakai; Adre, Cullen; Hussaini, Shehzana; Hembree, Carolyn; Lafferty, Allison G; Bernard, Shaina; Ruelle, Shannon; Loh, Mark P; Biochemistry, B S; Garner, Kimberly; Beganovic, Maya; GopalaSwamy, Ramesh
Source: Open Forum Infectious Diseases ; volume 13, issue Supplement_1 ; ISSN 2328-8957
Publisher Information: Oxford University Press (OUP)
Publication Year: 2026
Description: Wednesday, October 22, 2025: 11:30 AM Background: Serious adverse events (SAEs) related to ceftriaxone, a widely used cephalosporin antibiotic, are considered rare. After a 2024 SAE cluster in Alabama, the Centers for Disease Control and Prevention (CDC), with state/local partners and the US Food and Drug Administration (FDA), conducted a nationwide investigation of SAEs, including deaths, among patients who received ceftriaxone.Table.Clinical summary of serious adverse event cases (n=26), September 2024–June 2025Abbreviations: SAE: serious adverse event, ACH: acute care hospital, ED: emergency department, OP: outpatient clinic, F: female, M: male, Pt: patient (used when sex not reported); NR: not reported, NOS: not otherwise specified, EKG: electrocardiogram, PEA: pulseless electrical activity, IV: intravenous, IM: intramuscular, N/A: not applicable, PMH: past medical history, CA: cancer, CAD: coronary artery disease, CHF: congestive heart failure, CKD/ESRD: chronic kidney disease or end stage renal disease; COPD: chronic obstructive pulmonary disease, DM: diabetes mellitus, HTN: hypertension, HLD: hyperlipidemia, dx: disease CPR: cardiopulmonary resuscitation.Figure 1a-b.Epidemic curve: Frequency of reported serious adverse event cases following ceftriaxone administration from September 2024 to June 2025, by event month and US region (a) or ceftriaxone manufacturer (b), n=26Figure includes SAEs meeting CDC case definition: Adverse events following injectable ceftriaxone exposure, occurring after September 1, 2024, which: 1) occurred within 6 hours after receipt of injectable ceftriaxone in a non-ICU setting, 2) resulted in death or required cardiopulmonary resuscitation (CPR), and 3) were not attributed by the treating provider(s) to a cause other than ceftriaxone administration (such as known infection, other underlying medical condition, or exposure to a medication or medical product other than ceftriaxone). Figure 1a (left) displays epidemic curve by US Census Bureau region, reflecting case-patient ...
Document Type: article in journal/newspaper
Language: English
DOI: 10.1093/ofid/ofaf695.024
Availability: https://doi.org/10.1093/ofid/ofaf695.024; https://academic.oup.com/ofid/article-pdf/13/Supplement_1/ofaf695.024/66343447/ofaf695.024.pdf
Rights: https://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.13258502
Database: BASE