Vaccine side-effects and SARS-CoV-2 infection after vaccination in users of the COVID Symptom Study app in the UK: a prospective observational study

Cristina Menni(King's College London), Kerstin Kläser(King's College London), Anna May(ZOE (United Kingdom)), Lorenzo Polidori(ZOE (United Kingdom)), Joan Capdevila Pujol(ZOE (United Kingdom)), Panayiotis Louca(King's College London), Carole H. Sudre(King's College London), Long H. Nguyen(Harvard University), David A. Drew(Harvard University), Jordi Merino(Harvard University), Christina Hu(ZOE (United Kingdom)), Somesh Selvachandran(ZOE (United Kingdom)), Michela Antonelli(King's College London), Benjamin Murray(King's College London), Liane S. Canas(King's College London), Erika Molteni(King's College London), Mark S. Graham(King's College London), Marc Modat(King's College London), Amit D. Joshi(Massachusetts General Hospital), Massimo Mangino(Guy's and St Thomas' NHS Foundation Trust), Alexander Hammers(King's College London), Anna L. Goodman(Guy's and St Thomas' NHS Foundation Trust), Andrew T. Chan(Massachusetts General Hospital), Jonathan Wolf(ZOE (United Kingdom)), Claire J. Steves(King's College London), Ana M. Valdes(Nottingham Biomedical Research Centre), Sébastien Ourselin(King's College London), Tim D. Spector(King's College London)
The Lancet Infectious Diseases
April 27, 2021
Cited by 1,082Open Access
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Abstract

BACKGROUND: The Pfizer-BioNTech (BNT162b2) and the Oxford-AstraZeneca (ChAdOx1 nCoV-19) COVID-19 vaccines have shown excellent safety and efficacy in phase 3 trials. We aimed to investigate the safety and effectiveness of these vaccines in a UK community setting. METHODS: ), and comorbidities (binary variable, with or without comorbidities). FINDINGS: Between Dec 8, and March 10, 2021, 627 383 individuals reported being vaccinated with 655 590 doses: 282 103 received one dose of BNT162b2, of whom 28 207 received a second dose, and 345 280 received one dose of ChAdOx1 nCoV-19. Systemic side-effects were reported by 13·5% (38 155 of 282 103) of individuals after the first dose of BNT162b2, by 22·0% (6216 of 28 207) after the second dose of BNT162b2, and by 33·7% (116 473 of 345 280) after the first dose of ChAdOx1 nCoV-19. Local side-effects were reported by 71·9% (150 023 of 208 767) of individuals after the first dose of BNT162b2, by 68·5% (9025 of 13 179) after the second dose of BNT162b2, and by 58·7% (104 282 of 177 655) after the first dose of ChAdOx1 nCoV-19. Systemic side-effects were more common (1·6 times after the first dose of ChAdOx1 nCoV-19 and 2·9 times after the first dose of BNT162b2) among individuals with previous SARS-CoV-2 infection than among those without known past infection. Local effects were similarly higher in individuals previously infected than in those without known past infection (1·4 times after the first dose of ChAdOx1 nCoV-19 and 1·2 times after the first dose of BNT162b2). 3106 of 103 622 vaccinated individuals and 50 340 of 464 356 unvaccinated controls tested positive for SARS-CoV-2 infection. Significant reductions in infection risk were seen starting at 12 days after the first dose, reaching 60% (95% CI 49-68) for ChAdOx1 nCoV-19 and 69% (66-72) for BNT162b2 at 21-44 days and 72% (63-79) for BNT162b2 after 45-59 days. INTERPRETATION: Systemic and local side-effects after BNT162b2 and ChAdOx1 nCoV-19 vaccination occur at frequencies lower than reported in phase 3 trials. Both vaccines decrease the risk of SARS-CoV-2 infection after 12 days. FUNDING: ZOE Global, National Institute for Health Research, Chronic Disease Research Foundation, National Institutes of Health, UK Medical Research Council, Wellcome Trust, UK Research and Innovation, American Gastroenterological Association.


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