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dc.rights.licenseopenen_US
dc.contributor.authorPRETA, Laure-Helene
dc.contributor.authorCONTEJEAN, Adrien
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorSALVO, Francesco
dc.contributor.authorTRELUYER, Jean Marc
dc.contributor.authorCHARLIER, Caroline
dc.contributor.authorCHOUCHANA, Laurent
dc.date.accessioned2022-06-14T15:09:27Z
dc.date.available2022-06-14T15:09:27Z
dc.date.issued2022-07
dc.identifier.issn0306-5251en_US
dc.identifier.urioai:crossref.org:10.1111/bcp.15280
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/140215
dc.description.abstractEnSeveral cases of herpes zoster (HZ) following mRNA COVID-19 vaccination (BNT162b2 and mRNA-1273) have been reported, and the first epidemiological evidence suggests an increased risk. We used the worldwide pharmacovigilance database VigiBase to describe HZ cases following mRNA COVID-19 vaccination. We performed disproportionality analyses (case/non-case statistical approach) to assess the relative risk of HZ reporting in mRNA COVID-19 vaccine recipients compared to influenza vaccine recipients and according to patient age. To 30 June 2021, of 716 928 reports with mRNA COVID-19 vaccines, we found 7728 HZ cases. When compared to influenza vaccines, mRNA COVID-19 vaccines were associated with a significantly higher reporting of HZ (reporting odds ratio 1.9, 95% CI 1.8–2.1). Furthermore, we found a reduced risk of reporting HZ among under 40-year-old persons compared to older persons (reporting odds ratio 0.39, 95% CI 0.36–0.41). Mild and infrequent HZ reactions may occur shortly after mRNA COVID-19 vaccination, at higher frequency than reported with influenza vaccination, especially in patients over 40 years old. Further analyses are needed to confirm this risk.
dc.language.isoENen_US
dc.sourcecrossref
dc.subject.enCOVID-19
dc.subject.enDisproportionality
dc.subject.enHerpes zoster
dc.subject.enmRNA vaccines
dc.subject.enPharmacovigilance
dc.title.enAssociation study between herpes zoster reporting and mRNA COVID‐19 vaccines (BNT162b2 and mRNA‐1273)
dc.typeArticle de revueen_US
dc.identifier.doi10.1111/bcp.15280en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologie
dc.identifier.pubmed35174524en_US
bordeaux.journalBritish Journal of Clinical Pharmacologyen_US
bordeaux.page3529-3534en_US
bordeaux.volume88en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue7en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamAHEAD_BPHen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcedissemin
hal.identifierhal-03696617
hal.version1
hal.date.transferred2022-06-17T22:22:07Z
hal.exporttrue
workflow.import.sourcedissemin
dc.rights.ccPas de Licence CCen_US
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