Zdrowie i gospodarka · 20.11.2001

Vaccine Adverse Event Reporting System; Revised Form VAERS-2; Availability

The Food and Drug Administration (FDA) is announcing the availability of a proposed revised form entitled "Vaccine Adverse Event Reporting System" (Form VAERS-2) dated July 2001. This proposed revised form is intended to facilitate electronic reporting. The form has been revised by deleting data fields that FDA considers redundant or unnecessary, and by adding or revising data fields to ensure reporting clarity.