Factors influencing adverse events following COVID-19 vaccination
| Autor: | Paola Villanueva, Ellie McDonald, Julio Croda, Mariana Garcia Croda, Margareth Dalcolmo, Glauce dos Santos, Bruno Jardim, Marcus Lacerda, David J. Lynn, Helen Marshall, Roberto D. Oliveira, Jorge Rocha, Alice Sawka, Fernando Val, Laure F. Pittet, Nicole L. Messina, Nigel Curtis |
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| Jazyk: | angličtina |
| Rok vydání: | 2024 |
| Předmět: | |
| Zdroj: | Human Vaccines & Immunotherapeutics, Vol 20, Iss 1 (2024) |
| Druh dokumentu: | article |
| ISSN: | 21645515 2164-554X 2164-5515 |
| DOI: | 10.1080/21645515.2024.2323853 |
| Popis: | ABSTRACTVarious novel platform technologies have been used for the development of COVID-19 vaccines. In this nested cohort study among healthcare workers in Australia and Brazil who received three different COVID-19-specific vaccines, we (a) evaluated the incidence of adverse events following immunization (AEFI); (b) compared AEFI by vaccine type, dose and country; (c) identified factors influencing the incidence of AEFI; and (d) assessed the association between reactogenicity and vaccine anti-spike IgG antibody responses. Of 1302 participants who received homologous 2-dose regimens of ChAdOx1-S (Oxford-AstraZeneca), BNT162b2 (Pfizer-BioNTech) or CoronaVac (Sinovac), 1219 (94%) completed vaccine reaction questionnaires. Following the first vaccine dose, the incidence of any systemic reaction was higher in ChAdOx1-S recipients (374/806, 46%) compared with BNT162b2 (55/151, 36%; p = 0.02) or CoronaVac (26/262, 10%; p |
| Databáze: | Directory of Open Access Journals |
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