[Federal Register Volume 71, Number 77 (Friday, April 21, 2006)]
[Notices]
[Page 20708]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: E6-5970]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. 2001N-0464 (formerly Docket No. 01N-0464)]


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

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice; withdrawal.

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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revised form is being withdrawn because FDA is no longer pursuing 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.
[FR Doc. E6-5970 Filed 4-20-06; 8:45 am]
BILLING CODE 4160-01-S