Side Effects Following Administration of the First Dose of Oxford-AstraZeneca's Covishield Vaccine in Bangladesh: A Cross-Sectional Study

In response to the raging COVID-19 pandemic, Bangladesh started its vaccine administration in early 2021; however, due to the rapid development and launch of the vaccines in the market, many people had concerns regarding the safety of these vaccines. The purpose of this study was to evaluate the sid...

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Main Authors: Nishat Jahan (Author), Fahad Imtiaz Rahman (Author), Poushali Saha (Author), Sadia Afruz Ether (Author), ASM Roknuzzaman (Author), Rapty Sarker (Author), Khondoker Tashya Kalam (Author), Kashfa Haq (Author), Julkar Nyeen (Author), Humayra Zaman Himi (Author), Md. Nazmul Hossain (Author), Mahtab Hossain Chowdhury (Author), Mostafa Moin Uddin (Author), Nur Haque Alam (Author)
Format: Book
Published: MDPI AG, 2021-10-01T00:00:00Z.
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100 1 0 |a Nishat Jahan  |e author 
700 1 0 |a Fahad Imtiaz Rahman  |e author 
700 1 0 |a Poushali Saha  |e author 
700 1 0 |a Sadia Afruz Ether  |e author 
700 1 0 |a ASM Roknuzzaman  |e author 
700 1 0 |a Rapty Sarker  |e author 
700 1 0 |a Khondoker Tashya Kalam  |e author 
700 1 0 |a Kashfa Haq  |e author 
700 1 0 |a Julkar Nyeen  |e author 
700 1 0 |a Humayra Zaman Himi  |e author 
700 1 0 |a Md. Nazmul Hossain  |e author 
700 1 0 |a Mahtab Hossain Chowdhury  |e author 
700 1 0 |a Mostafa Moin Uddin  |e author 
700 1 0 |a Nur Haque Alam  |e author 
245 0 0 |a Side Effects Following Administration of the First Dose of Oxford-AstraZeneca's Covishield Vaccine in Bangladesh: A Cross-Sectional Study 
260 |b MDPI AG,   |c 2021-10-01T00:00:00Z. 
500 |a 10.3390/idr13040080 
500 |a 2036-7449 
520 |a In response to the raging COVID-19 pandemic, Bangladesh started its vaccine administration in early 2021; however, due to the rapid development and launch of the vaccines in the market, many people had concerns regarding the safety of these vaccines. The purpose of this study was to evaluate the side effects that were experienced by the Bangladeshi residents after receiving the first dose of the Oxford-AstraZeneca's Covishield vaccine (ChAdOx1nCoV-19). The study was conducted using both online and printed questionnaires and the data were analysed using SPSS. The results included the responses of 474 vaccine recipients from March-April 2021. Pain at the site of injection, fever, myalgia, fatigue and headache were the most commonly reported symptoms, and the overall side effects were found to be significantly more prevalent in the younger population (<i>p</i> ≤ 0.05). These findings were consistent with the results indicated by the clinical trial of ChAdOx1nCoV-19. Logistic regression analysis further revealed that compared to people aged 70 years or above, the incidence of reported side effects was significantly higher in people aged 18-30 years (odds ratio (OR) = 8.56), 31-40 years, (OR = 5.05), 41-50 years (OR = 4.08), 51-60 years (OR = 3.77) and 61-70 years (OR = 3.67). In addition, a significantly higher percentage of female participants suffered from post-vaccination side effects compared to males (OR = 1.51). It was concluded that the Covishield vaccine was well-tolerated among people of different age groups. Nevertheless, further long-term follow-up study with a larger sample size is warranted to establish the long-term safety of the COVID-19 vaccine. 
546 |a EN 
690 |a COVID-19 
690 |a Covishield 
690 |a Oxford-AstraZeneca 
690 |a post-vaccination side effects 
690 |a Other systems of medicine 
690 |a RZ201-999 
655 7 |a article  |2 local 
786 0 |n Infectious Disease Reports, Vol 13, Iss 4, Pp 888-901 (2021) 
787 0 |n https://www.mdpi.com/2036-7449/13/4/80 
787 0 |n https://doaj.org/toc/2036-7449 
856 4 1 |u https://doaj.org/article/1c60c042c39248b9996e6e45ef046553  |z Connect to this object online.