Adverse events following influenza A (H1N1) 2009 monovalent vaccines reported to the Vaccine Adverse Event Reporting System, United States, October 1, 2009-January 31, 2010

被引:98
作者
Vellozzi, Claudia [1 ]
Broder, Karen R. [1 ]
Haber, Penina [1 ]
Guh, Alice [1 ]
Nguyen, Michael [2 ]
Cano, Maria [1 ]
Lewis, Paige [1 ]
McNeil, Michael M. [1 ]
Bryant, Marthe [2 ]
Singleton, James [3 ]
Martin, David [2 ]
DeStefano, Frank [1 ]
机构
[1] Ctr Dis Control & Prevent, Immunizat Safety Off, Div Hlth Care Qual Promot, Natl Ctr Emerging & Zoonot Infect Dis, Atlanta, GA 30333 USA
[2] US FDA, Off Biostat & Epidemiol, Ctr Biol Evaluat & Res, Rockville, MD 20857 USA
[3] Ctr Dis Control & Prevent, Immunizat Serv Div, Natl Ctr Immunizat & Resp Dis, Atlanta, GA 30333 USA
关键词
H1N1; vaccines; Vaccine safety; Post-marketing surveillance; GUILLAIN-BARRE-SYNDROME; SAFETY; CHILDREN; IMMUNIZATION; INTUSSUSCEPTION; ASSOCIATION; ANAPHYLAXIS; ADULTS;
D O I
10.1016/j.vaccine.2010.09.021
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The United States (US) influenza A (H1N1) 2009 monovalent (2009-H1N1) vaccination program began in October 2009. Reports to the vaccine adverse event reporting system (VAERS), a US spontaneous reporting system, were reviewed to identify potential rare events or unusual adverse event (AE) patterns after 2009-H1N1 vaccination. The adverse event profile after 2009-H1N1 vaccine in VAERS (similar to 10,000 reports) was consistent with that of seasonal influenza vaccines, although the reporting rate was higher after 2009-H1N1 than seasonal influenza vaccines, this may be, at least in part, a reflection of stimulated reporting. Death, Guillain-Barre syndrome and anaphylaxis reports after 2009-H1N1 vaccination were rare (each <2 per million doses administered). Published by Elsevier Ltd.
引用
收藏
页码:7248 / 7255
页数:8
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