CDC Wonder Vaccine Adverse Event Reporting System

The Vaccine Adverse Event Reporting System (VAERS) online database on CDC WONDER provides counts and percentages of adverse event case reports after vaccination, received since January 1990 through last month. Data are available by symptom, vaccine product, manufacturer, onset interval, outcome category, year and month vaccinated, year and month reported, age, sex and state / territory. The Vaccine Adverse Event Reporting System is a cooperative program for vaccine safety of the Centers for Disease Control and Prevention (CDC) and the Food and Drug Administration (FDA). VAERS is a post-marketing safety surveillance program, collecting information about adverse events (possible side effects) that occur after the administration of US licensed vaccines. Data are from the US Department of Health and Human Services (DHHS), Public Health Service (PHS), Food and Drug Administration (FDA)/ Centers for Disease Control (CDC), Vaccine Adverse Event Reporting System (VAERS).

Data and Resources

Field Value
Groups
  • AmeriGEOSS
  • National Provider
  • North America
Tags
  • amerigeo
  • amerigeoss
  • ckan
  • geo
  • geoss
  • national
  • north-america
  • united-states
isopen False
license_id other-license-specified
license_title other-license-specified
maintainer admin
maintainer_email HealthData@hhs.gov
metadata_created 2025-11-29T13:44:10.211542
metadata_modified 2025-11-29T13:44:10.211546
notes <p>The Vaccine Adverse Event Reporting System (VAERS) online database on CDC WONDER provides counts and percentages of adverse event case reports after vaccination, received since January 1990 through last month. Data are available by symptom, vaccine product, manufacturer, onset interval, outcome category, year and month vaccinated, year and month reported, age, sex and state / territory. The Vaccine Adverse Event Reporting System is a cooperative program for vaccine safety of the Centers for Disease Control and Prevention (CDC) and the Food and Drug Administration (FDA). VAERS is a post-marketing safety surveillance program, collecting information about adverse events (possible side effects) that occur after the administration of US licensed vaccines. Data are from the US Department of Health and Human Services (DHHS), Public Health Service (PHS), Food and Drug Administration (FDA)/ Centers for Disease Control (CDC), Vaccine Adverse Event Reporting System (VAERS).</p>
num_resources 1
num_tags 8
title CDC Wonder Vaccine Adverse Event Reporting System