COVID-19 vaccines-related adverse events and associated factors reported among adult Egyptians

E. Ghazawy, A. Ewis, D. M. Khalil, S. Alkilany, Shaymaa Nafady, Hana Ewis, Momen Z. Mohammed, M. Abdelrehim
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Abstract

COVID-19 vaccine recipients are more likely to experience post-vaccination adverse events, which are considered the source of concerns about vaccine safety. This study aims to describe the utilization of COVID-19 vaccines and the associated adverse events and their possible predictors among adult Egyptians. An online cross-sectional study was designed to collect data through a Google Form questionnaire in November 2021. Adults who received at least one dose of the COVID-19 vaccine were asked to report their experience with vaccination and associated adverse events. A total of 853 participants were included in the study after receiving Sinopharm/Sinovac (63%), AstraZeneca (27%), Pfizer-BioNTech (4.8%), and other vaccines (5.2%). Around 50% of participants thought that COVID-19 vaccines were safe, 30.8% advised others with vaccination, and 68.3% reported post-vaccination adverse events. The most commonly encountered adverse symptoms were injection site pain (82.5%), fatigue (67.4%), flu-like symptoms (59.6%), and bone and muscle pains (59.6%). Most adverse events were less likely reported by Sinopharm/Sinovac recipients than recipients of other vaccines. The significant predictors for reporting adverse events were female gender, the first dose of vaccination, and vaccine type (AstraZeneca versus Sinopharm/Sinovac) with multivariable-adjusted OR (95% CI) = 1.85 (1.34-2.54); 2.01 (1.24–3.25), and 3.86 (2.54–5.86). Findings revealed that adverse events of COVID-19 vaccines are common. Sinopharm/Sinovac recipients were reported to have lesser adverse events than other recipients. However, serious reactions were rare which ensures the safety of all vaccine types among the adult Egyptian population.
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埃及成年人中报告的COVID-19疫苗相关不良事件及相关因素
COVID-19疫苗接种者更有可能出现疫苗接种后不良事件,这被认为是疫苗安全性问题的根源。本研究旨在描述埃及成年人COVID-19疫苗的使用情况、相关不良事件及其可能的预测因素。一项在线横断面研究旨在于2021年11月通过谷歌表单问卷收集数据。接受至少一剂COVID-19疫苗的成年人被要求报告他们的疫苗接种经历和相关不良事件。共有853名受试者在接受了国药/科兴(63%)、阿斯利康(27%)、辉瑞- biontech(4.8%)和其他疫苗(5.2%)后纳入研究。约50%的参与者认为COVID-19疫苗是安全的,30.8%的参与者建议他人接种疫苗,68.3%的参与者报告了疫苗接种后的不良事件。最常见的不良症状是注射部位疼痛(82.5%)、疲劳(67.4%)、流感样症状(59.6%)和骨骼和肌肉疼痛(59.6%)。大多数不良事件由国药/科兴疫苗接种者报告的可能性低于其他疫苗接种者。不良事件报告的显著预测因子为女性性别、首次接种疫苗剂量和疫苗类型(阿斯利康vs国药/科兴),多变量校正OR (95% CI) = 1.85 (1.34-2.54);2.01(1.24-3.25)和3.86(2.54-5.86)。调查结果显示,COVID-19疫苗的不良事件很常见。据报道,与其他接受者相比,国药/科兴接受者的不良事件较少。然而,严重的反应很少,这确保了所有类型的疫苗在埃及成年人口中的安全性。
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来源期刊
Journal of Public Health and Development
Journal of Public Health and Development Social Sciences-Health (social science)
CiteScore
0.50
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0.00%
发文量
64
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