| アブストラクト | BACKGROUND: REBYOTA and VOWST are the first FDA-approved live biotherapeutic products (LBPs) for recurrent Clostridioides difficile infection (rCDI). Prior FDA safety alerts (2019-2020) regarding invasive infections from investigational fecal microbiota transplantation underscore the need for post-marketing surveillance of these novel products. AIMS: To characterize the real-world safety profiles of REBYOTA and VOWST using the FDA Adverse Event Reporting System (FAERS) and compare them against established CDI therapeutics. METHODS: We performed disproportionality analysis of FAERS data (Q1;2020-Q4;2025). REBYOTA and VOWST were identified as primary suspect drugs using BLA numbers and drug name matching. Comparators included fidaxomicin, bezlotoxumab, and vancomycin (CDI-filtered). Four methods were applied: reporting odds ratio (ROR), proportional reporting ratio, information component, and empirical Bayes geometric mean. Signals required >/=2 methods agreement. RESULTS: We identified 231 REBYOTA and 813 VOWST primary suspect reports, yielding 18 and 54 disproportionality signals, respectively. Both products' signals were consistent with known gastrointestinal adverse events. No signals were detected for bacteremia, septic shock, or anaphylaxis. Death was reported at lower-than-expected frequency for VOWST (ROR 0.29; 95% CI 0.15-0.53). A VOWST-specific UTI cluster (Klebsiella UTI ROR 405.73; Pseudomonal UTI ROR 168.54) was identified; head-to-head comparison showed no significant UTI difference versus REBYOTA (ROR 1.39, NS), suggesting stimulated reporting bias rather than a biological signal. Route-dependent adverse event profiles differed between oral VOWST and rectal REBYOTA. CONCLUSIONS: FDA-approved LBPs demonstrate reassuring post-marketing safety profiles without transmitted infection signals. The extreme VOWST UTI signal is likely attributable to FDA-mandated expedited reporting obligations rather than a causal drug effect. |
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| ジャーナル名 | The American journal of gastroenterology |
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| Pubmed追加日 | 2026/7/21 |
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| 投稿者 | Gong, Eun Jeong; Bang, Chang Seok; Lee, Jae Jun; Baik, Gwang Ho |
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| 組織名 | Department of Internal Medicine, Hallym University College of Medicine,;Chuncheon, Korea.;Institute for Liver and Digestive Diseases, Hallym University, Chuncheon, Korea.;Institute of New Frontier Research, Hallym University College of Medicine,;Department of Anesthesiology and Pain Medicine, Hallym University College of;Medicine, Chuncheon, Korea. |
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| Pubmed リンク | https://www.ncbi.nlm.nih.gov/pubmed/42479871/ |
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