Investigation of Reported Anaphylaxis Post COVID-19 Vaccination in Subjects with History of Allergies and Anaphylaxis

Aditya P. Desai, Aryan P. Desai, Victoria Ochs, Prashant V. Desai
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Abstract

Two mRNA COVID-19 vaccines, Pfizer-BioNTech and Moderna, are currently approved in the United States, and one viral-vector vaccine, J&J/Janssen, is authorized for limited use. The Vaccine Adverse Event Reporting System (VAERS) database gathers reports of adverse effects, including anaphylaxis. In this manuscript, we provide a summary of reported incidence of anaphylaxis rates following administration of the two mRNA and one viral-vector COVID-19 vaccine. A detailed investigation of the relative risk of anaphylaxis for recipients with or without a prior history of allergy and/or anaphylaxis is also described. Overall reported incidence of anaphylaxis is 4.49 [95% CI: 0.25 – 8.73] cases per million doses administered. The reported risk of anaphylaxis is 1.83 times greater for recipients with prior allergies and no anaphylaxis but 17.70 times greater for recipients with prior allergies and anaphylaxis.
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有过敏史和过敏反应的受试者接种COVID-19疫苗后报告过敏反应的调查
两种mRNA - COVID-19疫苗辉瑞- biontech和Moderna目前已在美国获得批准,一种病毒载体疫苗强生/杨森获批有限使用。疫苗不良事件报告系统(VAERS)数据库收集不良反应报告,包括过敏反应。在这篇文章中,我们总结了两种mRNA和一种病毒载体COVID-19疫苗接种后报告的过敏反应发生率。对有或没有过敏史和/或过敏反应的接受者的相对风险的详细调查也被描述。总体报告的过敏反应发生率为4.49 [95% CI: 0.25 - 8.73]例/百万剂量。报告的过敏反应风险对于有过敏史和无过敏史的接受者是1.83倍,而对于有过敏史和过敏史的接受者是17.70倍。
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