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

作者： Claudia Vellozzi , Karen R. Broder , Penina Haber , Alice Guh , Michael Nguyen

DOI: 10.1016/J.VACCINE.2010.09.021

关键词:

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 system, were reviewed identify potential rare events or unusual (AE) patterns after 2009-H1N1 vaccination. profile VAERS (∼10,000 reports) was consistent with that of seasonal vaccines, although rate higher than this may be, at least part, reflection stimulated reporting. Death, Guillain-Barre syndrome and anaphylaxis reports (each <2 per million doses administered).

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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

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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

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