Announcement: Implementation of the Vaccine Adverse Event Reporting System 2.0 Reporting Form

Details

• Journal Article:
  Morbidity and Mortality Weekly Report (MMWR)
• 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:
  Adverse Drug Reaction Reporting Systems Announcement Humans Vaccines
• Source:
  MMWR Morbidity Mortal Weekly Rep. 66(27):738.
• Series:
  Weekly Report: Morbidity and Mortality Weekly Report (MMWR)
• DOI:
  http://dx.doi.org/10.15585/mmwr.mm6627a5
• ISSN:
  0149-2195 (print) ; 1545-861X (digital)
• Pubmed ID:
  28704349
• Pubmed Central ID:
  PMC5687587
• Document Type:
  Journal Article
• Name as Subject:
  Vaccine Adverse Event Reporting System
• Place as Subject:
  United States
• Pages in Document:
  1 pdf page
• Volume:
  66
• Issue:
  27
• Collection(s):
  Morbidity and Mortality Weekly Report (MMWR)
• Main Document Checksum:
  urn:sha-512:0375a2f877ce4d180f3c999e7fda258a522970153b5707575ea2678c2035eecf35b6850a4fd7ec8232a68ed14307a7ae20e69414f78d6d955299d0f94e7d9f00
• Download URL:
  https://stacks.cdc.gov/view/cdc/54549/cdc_54549_DS1.pdf
• File Type:
  [PDF - 105.51 KB ]