A Survey of the Side Effects of Pfizer/BioNTech COVID-19 Vaccine among Vaccinated Adults in Iraq

IF 0.6 Q4 Health Professions
Abubakir Saleh, N. Shabila
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Abstract

Background: Pfizer-BioNTech vaccine was one of the first vaccines developed for COVID-19 to be used in Iraq. While the benefits of the vaccine outweigh the risks, potential side effects remain major concerns for people and can increase vaccine hesitancy despite usually being short-lasting and mild. This study aimed to evaluate the side effects of Pfizer-BioNTech vaccination among vaccinated adults in Erbil city, Iraq. Methods: A cross-sectional study was carried out with a convenience sample of 401 subjects who received the Pfizer vaccine in nine public healthcare centres in Erbil, Iraq, on February 20th, 2022, and April 17th 2022. Data was collected through interviews with the patients using a questionnaire designed by the researchers; a p-value ≤ 0.05 was considered statistically significant. Results: The prevalence of side effects was 84.4%. Among participants who experienced side effects, the most common was pain at the injection site (93.1% for the first dose and 88% for the second dose). For the first dose, the onset of side effects on the vaccination day (day zero) was reported by 78.9% of those experiencing side effects, and the duration was one day for 45.4% of participants. Severity was rated as mild by 54.3%, and similar results were found for the second dose. Analgesics were used following the first dose by 47% of participants, which resulted in good relief for 96.6% of patients using them, and similar results were found for the second dose. Conclusions: Most participants who received the Pfizer-BioNTech vaccine experienced side effects, the most common of which was pain at the injection site, which was reported for both the first and second doses.
伊拉克接种辉瑞/生物技术公司 COVID-19 疫苗的成人副作用调查
背景:辉瑞- biontech疫苗是首批在伊拉克使用的COVID-19疫苗之一。虽然疫苗的益处大于风险,但潜在的副作用仍然是人们主要关注的问题,尽管通常持续时间短且轻微,但可能会增加对疫苗的犹豫。本研究旨在评估在伊拉克埃尔比勒市接种了辉瑞- biontech疫苗的成年人的副作用。方法:采用横断面研究方法,选取于2022年2月20日和2022年4月17日在伊拉克埃尔比勒市9个公共卫生中心接种辉瑞疫苗的401名受试者作为方便样本。数据是通过使用研究人员设计的问卷与患者进行访谈来收集的;p值≤0.05认为有统计学意义。结果:副反应发生率为84.4%。在有副作用的参与者中,最常见的是注射部位疼痛(第一次剂量为93.1%,第二次剂量为88%)。对于第一剂,78.9%的出现副作用的人报告在接种疫苗当天(第0天)出现副作用,45.4%的参与者报告副作用持续时间为一天。54.3%的严重程度被评为轻度,第二次剂量的结果相似。47%的参与者在第一次给药后使用了镇痛药,96.6%的患者使用了镇痛药,第二次给药时也发现了类似的结果。结论:大多数接受辉瑞- biontech疫苗的参与者都出现了副作用,其中最常见的是注射部位疼痛,这在第一次和第二次剂量中都有报道。
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来源期刊
Asia Pacific Journal of Health Management
Asia Pacific Journal of Health Management HEALTH POLICY & SERVICES-
CiteScore
1.10
自引率
16.70%
发文量
51
审稿时长
9 weeks
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