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. 2022 Feb 21;94(6):2453–2459. doi: 10.1002/jmv.27655

Table 3.

Types of AEFI reported among the study participants (N = 1826)

Type of AEFI Total (N = 1826), N (%) First dose (N = 23), N (%) Second dose (N = 1303), N (%) value
Pain at the injection site 267 (14.6) 134 (25.6) 133 (10.2) <0.001
Tenderness/soreness 78 (4.3) 23 (4.4) 55 (4.2) 0.898
Redness/erythema 4 (0.2) 1 (0.2) 3 (0.2) 1.000
Swelling/induration 11 (0.6) 6 (1.1) 5 (0.4) 0.057
Itching/pruritus associated with injection 1 (0.1) 1 (0.2) 0 (0.0) 0.286
Pain 10 (0.5) 5 (1.0) 5 (0.4) 0.134
Fever 178 (9.7) 55 (10.5) 123 (9.4) 0.483
Nausea/vomiting 8 (0.4) 4 (0.8) 4 (0.3) 0.181
Headache 104 (5.7) 37 (7.1) 67 (5.1) 0.107
Fatigue 88 (4.8) 19 (3.6) 69 (5.3) 0.134
Muscle pain/myalgia 107 (5.9) 27 (5.2) 80 (6.1) 0.422
Rash 13 (0.7) 1 (0.2) 12 (0.9) 0.094
Joint pain 2 (0.1) 2 (0.4) 0 (0.0) 0.026
Others 3 (0.1) 1 (0.2) 2 (0.2) 0.857
Individuals having any AEFI 544 (29.8) 199 (38.1) 345 (26.4) <0.001

Abbreviation: AEFI, adverse events following immunization.