Smallpox vaccine adverse events among civilians--United States, March 4-10, 2003.
MMWR Morb Mortal Wkly Rep. 2003 Mar 14; 52(10):201-3.MM

Abstract

During the civilian smallpox vaccination program, CDC, the Food and Drug Administration, and state health departments are conducting surveillance for vaccine-associated adverse events. In the first stage of the program, active surveillance is being conducted for potentially life-threatening, moderate-to-severe, and other serious adverse events and for vaccinia transmission to contacts of vaccinees (Table). Nonserious events are reported through passive surveillance and are expected to be underreported. This report summarizes smallpox vaccine adverse events reported among civilians vaccinated as of March 7, 2003, and among contacts of vaccinees, received by CDC from the Vaccine Adverse Event Reporting System (VAERS) as of March 10.

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Publisher Full Text

Authors

Centers for Disease Control and Prevention (CDC)
No affiliation info available

MeSH

AdultAdverse Drug Reaction Reporting SystemsFemaleHealth PersonnelHumansMaleMiddle AgedMilitary PersonnelPopulation SurveillanceSmallpox VaccineUnited StatesVaccination

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

12653459