Skip to content
LexBuild

Vaccine Adverse Event Reporting; Revised Form VAERS-2; Withdrawal of Proposed Revised Form

---
identifier: "/us/fr/E6-5970"
source: "fr"
legal_status: "authoritative_unofficial"
title: "Vaccine Adverse Event Reporting; Revised Form VAERS-2; Withdrawal of Proposed Revised Form"
title_number: 0
title_name: "Federal Register"
section_number: "E6-5970"
section_name: "Vaccine Adverse Event Reporting; Revised Form VAERS-2; Withdrawal of Proposed Revised Form"
positive_law: false
currency: "2006-04-21"
last_updated: "2006-04-21"
format_version: "1.1.0"
generator: "[email protected]"
agency: "Health and Human Services Department"
document_number: "E6-5970"
document_type: "notice"
publication_date: "2006-04-21"
agencies:
  - "Health and Human Services Department"
  - "Food and Drug Administration"
fr_citation: "71 FR 20708"
fr_volume: 71
docket_ids:
  - "Docket No. 2001N-0464 (formerly Docket No. 01N-0464)"
fr_action: "Notice; withdrawal."
---

#  Vaccine Adverse Event Reporting; Revised Form VAERS-2; Withdrawal of Proposed Revised Form

**AGENCY:**

Food and Drug Administration, HHS.

**ACTION:**

Notice; withdrawal.

**SUMMARY:**

The Food and Drug Administration (FDA) is announcing the withdrawal of a proposed revised form that was issued in the *Federal Register* on November 20, 2001.

**DATES:**

April 21, 2006.

**FOR FURTHER INFORMATION CONTACT:**

Joseph L. Okrasinski, Jr., Center for Biologics Evaluation and Research (HFM-17), Food and Drug Administration, 1401 Rockville Pike, Suite 200N, Rockville, MD 20852-1448, 301-827-6210.

**SUPPLEMENTARY INFORMATION:**

In a notice published in the *Federal Register* of November 20, 2001 (66 FR 58153), FDA announced the availability of a proposed revised form entitled “Vaccine Adverse Event Reporting System” (Form VAERS-2) dated July 2001. This proposed revised form is being withdrawn because FDA is no longer pursuing changes to the form.

Dated: April 12, 2006.

Jeffrey Shuren,

Assistant Commissioner for Policy.