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Announcement: Implementation of the Vaccine Adverse Event Reporting System 2.0 Reporting Form
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Jul 14 2017
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Source: MMWR Morbidity Mortal Weekly Rep. 66(27):738.
[PDF-105.51 KB]
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Journal Article:Morbidity and Mortality Weekly Report (MMWR)
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Description:The Vaccine Adverse Event Reporting System (VAERS), co-managed by CDC and the Food and Drug Administration (FDA), is the national postmarketing safety monitoring system that accepts reports about adverse events that occur after administration of U.S.-licensed vaccines (1,2). On June 30, 2017, CDC and FDA implemented a revised reporting form and a new process for submitting reports to VAERS. Persons reporting adverse events are now able to use the VAERS 2.0 online reporting tool to submit reports directly online; alternatively, they may download and complete the writable and savable VAERS 2.0 form and submit it using an electronic document upload feature.
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ISSN:0149-2195 (print);1545-861X (digital);
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Pubmed ID:28704349
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Pubmed Central ID:PMC5687587
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Pages in Document:1 pdf page
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Volume:66
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Issue:27
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