Active telephone surveillance to evaluate adverse events among civilian smallpox vaccine recipients

Vaccine. 2006 Jan 23;24(4):476-84. doi: 10.1016/j.vaccine.2005.07.089. Epub 2005 Aug 30.

Abstract

Objective: Better characterize and monitor adverse events following Dryvax vaccinia vaccination in civilian health care workers and other first responders.

Design: Telephone interviews to ascertain adverse events experienced.

Results: Eight hundred twenty-five vaccinees, including 44 in the comparison group, were interviewed. At 10 days, 71.4% reported blisters, 35.1% reported bumps at the vaccination site, 48.5% swelling, 47.3% scab, tiredness/lethargy/fatigue (43.6%), headache (34.2%), lymph node swelling/tenderness (28.5%), muscle pain (23.1%), chills (14.4%), joint pain 11.8%, and fever >100 degrees F (12.5%). The 12.5% reported missing work because of vaccine adverse events. Most adverse events were anticipated and of short duration.

MeSH terms

  • Adverse Drug Reaction Reporting Systems
  • Contraindications
  • Humans
  • Interviews as Topic
  • Population Surveillance
  • Public Health Practice / standards*
  • Smallpox Vaccine / adverse effects*
  • Vaccination / adverse effects*

Substances

  • Smallpox Vaccine