Table 4. Reactions and Health Impacts Reported in v-safe Respondents.
Reaction | Simultaneous influenza and COVID-19 mRNA booster vaccine received, aOR (95% CI)a,b (N = 92 023) | |
---|---|---|
Pfizer-BioNTech (n = 61 390) | Moderna (n = 30 633) | |
Any injection site reaction | 1.10 (1.08-1.12) | 1.05 (1.02-1.08) |
Any systemic reaction | 1.08 (1.06-1.10) | 1.11 (1.08-1.14) |
Any health impactc | 0.99 (0.97-1.02) | 1.05 (1.02-1.08) |
Unable to perform normal daily activities | 0.99 (0.97-1.01) | 1.04 (1.01-1.07) |
Unable to work or attend school | 1.04 (1.01– 1.07) | 1.08 (1.04-1.12) |
Needed medical care | 0.92 (0.84-1.01) | 0.94 (0.83-1.07) |
Includes persons who completed at least one v-safe health check-in survey on days 0 to 7 after vaccination. Odds ratios were adjusted for age at vaccination, sex, and week of vaccination.
Simultaneous vaccination was defined as persons who received a COVID-19 mRNA booster vaccine and seasonal influenza vaccine during the same visit. A booster dose was defined as dose 3 of a COVID-19 mRNA vaccine administered ≥5 months after dose 2, on or after booster doses were authorized for each manufacturer and age group.
Any health impact was defined as persons who reported they were unable to perform normal daily activities, missed work or school, or received care from a medical professional because of new symptoms or conditions.