[Federal Register: April 21, 2006 (Volume 71, Number 77)] [Notices] [Page 20708] From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:fr21ap06-69] ----------------------------------------------------------------------- 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. ----------------------------------------------------------------------- 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 This proposed revised form is being withdrawn because FDA is no longer pursuing changes to the form.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