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The Vaccine Adverse Event Reporting System (VAERS) Request

This is a saved request
Saved May 9, 2017, 5:39 PMMore Information
the link that creates this page
  • This dataset has been updated since this request was saved, which could lead to differences in results.
Dataset Documentation Other Data AccessData Use RestrictionsHow to Use WONDER
Make all desired selections and then click any Send button one time to send your request.
1. Organize table layout:Help
Notes:
• Data contains VAERS reports processed as of 6/14/2017.
• Must group by VAERS ID when selecting any of the Optional Measures.
• When grouping by VAERS ID, results are initially displayed with Events Reported, Percent, and totals not shown.
Optional Measures (Check box to include in results.)
 
 
 
 
 
 
 
DISCLAIMER: VAERS staff at CDC and the Food and Drug Administration (FDA) follow up on all serious adverse event reports to obtain additional medical, laboratory, and/or autopsy records to help understand the circumstances. However, VAERS public data do not generally change based on the information obtained during the follow-up process. There are limitations to VAERS data. A report to VAERS does not mean that the vaccine caused the adverse event, only that the adverse event occurred sometime after vaccination. Read more about interpreting VAERS data: More information.
2. Select symptoms:Help
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Items in the Selected Items box will be used for your request.
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Leave box empty, or use *All*, to select all values.