Abstract
Concern about side effects constitutes a major deterrent to patient compliance with influenza vaccination, yet there is a paucity of data about the occurrence of adverse reactions in the population targeted for immunization. We conducted a randomized, double-blind, crossover trial to compare the frequency of adverse reactions following administration of 1988-1989 trivalent split-antigen influenza vaccine and saline placebo. Outpatient veterans 65 years of age or over (n = 336) were recruited by mail and were randomly assigned to receive vaccine followed 2 weeks later by placebo injection or placebo followed 2 weeks later by vaccine. There was no significant difference between influenza vaccine and placebo with respect to the proportion of subjects reporting disability or systemic symptoms.
Original language | English (US) |
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Pages (from-to) | 1139-1141 |
Number of pages | 3 |
Journal | JAMA: The Journal of the American Medical Association |
Volume | 264 |
Issue number | 9 |
DOIs | |
State | Published - Sep 5 1990 |
ASJC Scopus subject areas
- Medicine(all)