Serious adverse events rarely reported after trivalent inactivated influenza vaccine (TIV) in children 6-23 months of age

被引:31
作者
Rosenberg, Melissa
Sparks, Robert
McMahon, Ann [3 ]
Iskander, John [4 ]
Campbell, James D. [1 ]
Edwards, Kathryn M. [2 ]
机构
[1] Univ Maryland, Ctr Vaccine Dev, Sch Med, Dept Pediat, Baltimore, MD 21201 USA
[2] Vanderbilt Univ, Vanderbilt Vaccine Res Program, Sarah H Sell Chair Pediat, Nashville, TN 37232 USA
[3] US FDA, Div Adverse Event Anal 2, Off Surveillance & Epidemiol, CDER, Silver Spring, MD USA
[4] Ctr Dis Control & Prevent, Immunizat Safety Off, Off Chief Sci Officer, Atlanta, GA USA
关键词
Trivalent influenza vaccine; Vaccine Adverse Event Reporting System; Advisory Committee on Immunization; Practices; Serious adverse event; Causality; ANTHRAX VACCINE; SAFETY; BURDEN; SYSTEM; ILLNESS; AVEC;
D O I
10.1016/j.vaccine.2009.05.023
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In October 2003 the Advisory Committee on Immunization Practices (ACIP) recommended influenza vaccination for all children ages 6-23 months. We evaluated the safety of this recommendation by querying the Vaccine Adverse Events Reporting System (VAERS) for serious adverse events (SAE) reported between July 1, 2003 and June 30, 2006 in 6-23 month old infants after trivalent inactivated influenza vaccine (TIV). Cases were reviewed and the causal relationship with vaccine assessed. One hundred and four SAE were reported: median time from vaccination to SAE onset was one day. The two most commonly reported SAE disease categories were fever (N=52) and seizure (N=35). Causality assessment revealed that none of the SAE was definitely related to TIV. Although the number of SAE increased over time, the most common types of events remained unchanged with no new or unexpected safety concerns identified with expanded TIV use. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4278 / 4283
页数:6
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