High COVID‑19 volume did not align with its weak signal, while strong signals for the Lyme disease, rubella, and anthrax vaccines reflected specific populations, and no strong disproportionality signal was found.
Abstract
ABSTRACT Vaccination is a principal method of infectious disease prevention, but its association with rheumatoid arthritis (RA) remains controversial. This study assessed vaccine‑associated RA using the Vaccine Adverse Event Reporting System (VAERS). Data from 1990 to 2026 were extracted. Descriptive statistics, Weibull fitting, and disproportionality analysis using four methods, including the reporting odds ratio (ROR), along with subgroup analyses by age, sex, and pre‑/post‑COVID, were performed. Among 11,532,185 reports, 34,498 RA‑related adverse events (AEs) (0.03%) involved 5006 subjects. Females comprised 77.9% and 18–65 predominated. Serious outcomes occurred in 13.48%. Most AEs (47.49%) were musculoskeletal. 47.0% occurred within 7d (median 5.4), indicating early failure. The COVID‑19 vaccine had the most reports (n = 24,266) but a weak signal (ROR = 1.25); the Lyme disease vaccine (ROR = 27.81), the rubella vaccine (ROR = 5.69), and the anthrax vaccine (ROR = 3.90) exhibited the strongest signals. Subgroup signals: Lyme disease vaccine except 2021–2026; rubella vaccine only in females/≤17; anthrax vaccine in 18–64. RA‑related vaccine AEs are extremely rare, mainly musculoskeletal and within 1 week. High COVID‑19 volume did not align with its weak signal, while strong signals for the Lyme disease, rubella, and anthrax vaccines reflected specific populations. No strong disproportionality signal was found. However, VAERS is passive, cannot establish causality or confirm safety.
ABSTRACT Dupilumab is effective for the treatment of moderate‑to‑severe type 2 inflammatory diseases; however, its real‑world safety profile in pediatric patients remains to be further clarified. This retrospective pharmacovigilance study analyzed U.S. Food and Drug Administration Adverse Event Reporting System (FAERS)...
Xue-Qing Ma, Jiao-Jiao Fan, Ben Liu· Human Vaccines & Immunothera...· 2 citations
A retrospective pharmacovigilance study using FAERS data covering the period from 2004 Q1 to 2025 Q4 reveals a strong signal of haematological toxicity associated with antitumour agents, supporting enhanced routine monitoring to mitigate clinical risks.
Xing-Nong Xu, Lei Ma· Frontiers in Immunology· 0 citations
OBJECTIVE
We aimed to assess the association between COVID-19 vaccination status and COVID-19-related hospital admissions, need for mechanical ventilation or extracorporeal membrane oxygenation (ECMO), and death in people with autoimmune rheumatic conditions.
METHODS
We conducted a retrospective cohort study using Na...
Lesley E. Jackson, A. J. Anzalone, K. Saag et al.· Arthritis & Rheumatology· 0 citations
INTRODUCTION
Infection-related adverse events are an important safety concern in psoriasis therapy.
OBJECTIVE
To compare infection-related adverse-event reporting across mechanism-based therapy groups.
METHODS
We analyzed psoriasis-indicated US Food and Drug Administration Adverse Event Reporting System (FAERS) rep...
Shinwon Hwang, Yerim Kwak, Ye-On-Woo Jung et al.· Journal of dermatological tr...· 0 citations
PURPOSE
Dupilumab is a human monoclonal antibody used to treat various inflammatory conditions. The purpose of this study was to characterize the cumulative proportion of documented ocular adverse events after dupilumab initiation and compare outcomes between patients with atopic dermatitis (AD) and those treated for n...
Osama Elaraby, Karen M. Wai, Q. Nguyen et al.· Cornea· 0 citations
Eribulin is used to treat metastatic breast cancer, but its adverse event (AE) profile requires comprehensive analysis using FDA Adverse Event Reporting System (FAERS) data to guide clinical use. We analyzed eribulin-related AE reports in FAERS (Q1 2011 - Q2 2024). Disproportionality analyses (ROR, PRR, MGPS, BCPNN) id...
Yao Zhou, Jie Gong, Le-Le Shen et al.· PLoS ONE· 0 citations
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