A longitudinal study to estimate adverse events following two doses of COVID-19 vaccination
Autor: | Saurabh Bobdey, Rajesh Sahu, Arun Kumar Yadav, S K Kaushik, K S Sreekanth, Niharika Nagari, Kunal Koundinya |
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Jazyk: | angličtina |
Rok vydání: | 2022 |
Předmět: | |
Zdroj: | Medical Journal of Dr. D.Y. Patil Vidyapeeth, Vol 15, Iss 8, Pp 334-338 (2022) |
Druh dokumentu: | article |
ISSN: | 2589-8302 2589-8310 |
DOI: | 10.4103/mjdrdypu.mjdrdypu_722_21 |
Popis: | Background: On March 30, 2020, coronavirus disease 19 was declared pandemic and many countries of the world started working on the development of vaccine soon after China released the genetic structure of severe acute respiratory syndrome coronavirus 2. Drugs Controller General of India on January 3, 2021, accorded emergency use authorization to Oxford-AstraZeneca's ChAdOx1 nCoV-19 vaccine and vaccination drive commenced in India on January 16, 2021. The present study was conducted to determine the incidence adverse event following immunization (AEFI) among recipients of the first and second dose of the vaccine. Materials and Methods: A longitudinal descriptive study was conducted among 2529 vaccine beneficiaries who were asked about the side effects at 24 and 72 h after the first dose and second dose of vaccination with ChAdOx1 nCoV-19 vaccine. Passive surveillance was also done for 4 months. Results: AEFI was reported in 27.59%, 38.4%, and 19.96% of vaccines after both doses, first dose, and second dose, respectively. 14% did not report any AEFI with either dose of vaccine. Younger people had higher rates of AEFIs with both the doses. Pain at injection site and fever |
Databáze: | Directory of Open Access Journals |
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