TMPPM 2008 > Appendices > Immunizations > Immunizations Overview

H.1.1 Vaccine Adverse Event Reporting System (VAERS)

The National Childhood Vaccine Injury Act of 1986 (NCVIA) requires health-care providers to report:

•Any reaction listed by the vaccine manufacturer as a contraindication to subsequent doses of the vaccine.

•Any reaction listed in the Reportable Events Table that occurs within the specified time period after vaccination.

•A copy of the Reportable Events Table can be obtained by calling VAERS at 1-800-822-7967 or by downloading it from vaers.hhs.gov/pubs.htm.

Clinically significant adverse events should be reported even if it is unclear whether a vaccine caused the event.

Note: Documentation of the injection site is recommended, but not required. For additional information regarding documentation, providers can refer to www.hrsa.gov/vaccinecompensation/filing_claim.htm and www.cdc.gov/od/science/iso/professional_info
/providers_role.htm.