i
Announcement: Implementation of the Vaccine Adverse Event Reporting System 2.0 Reporting Form
-
Jul 14 2017
Source: MMWR Morb Mortal Wkly Rep. 66(27):738.
Details:
-
Alternative Title:MMWR Morb Mortal Wkly Rep
-
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.
-
Subjects:
-
Pubmed ID:28704349
-
Pubmed Central ID:PMC5687587
-
Document Type:
-
Name as Subject:
-
Place as Subject:
-
Collection(s):
-
Main Document Checksum:
-
Download URL:
-
File Type: