Ontology highlight
ABSTRACT: Objective
To assess the short term safety of the COVID-19 vaccines Comirnaty (Pfizer-BioNTech BNT162b2) and Vaxzevria (AstraZeneca ChAdOx1) in Australia.Design
Prospective observational cohort study; online surveys by AusVaxSafety, a national active vaccine safety surveillance system, three and eight days after vaccination.Setting, participants
People aged 16 years or more who received COVID-19 vaccines at sentinel vaccination hubs, general practices, or Aboriginal Community Controlled Health Organisation clinics, 22 February - 30 August 2021.Main outcome measures
Primary outcome: proportion of respondents who reported any adverse event following immunisation (AEFI) 0-3 days after vaccination.Secondary outcomes
proportions of respondents who reported
SUBMITTER: Deng L
PROVIDER: S-EPMC9350119 | biostudies-literature | 2022 Aug
REPOSITORIES: biostudies-literature