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. 2022 Oct 11;22:780. doi: 10.1186/s12879-022-07765-w

Table 1.

characteristics and adverse reactions of participants

EC TST P
number 7351 (50.4%) 7228 (49.6%)
male 49.1% (3606/7351) 47.4% (3423/7228) 0.04
age 18.1 ± 0.8 18.1 ± 0.7 0.77
BMI 20.9 ± 3.1 20.9 ± 3.2 0.99
total ADR 1565 (21.3%) 2499 (34.6%) 0.000
bleeding 414 (5.63%) 467 (6.46%) 0.036
dermatodyschroia 314 (4.27%) 440 (6.09%) 0.000
induration 287 (3.90%) 933 (12.91%) 0.000
swelling 183 (2.49%) 258 (3.57%) 0.000
pain 117(1.59%) 115(1.59%) 0.998
pruritus 109 (1.48%) 112 (1.55%) 0.742
erythema 48(0.65%) 76(1.05%) 0.009
blistering 30 (0.41%) 27 (0.37%) 0.738
fatigue 18 (0.24%) 12 (0.17%) 0.294
headache 10 (0.14%) 12 (0.17%) 0.641
rash 9 (0.12%) 14 (0.19%) 0.278
nausea 6 (0.08%) 11 (0.15%) 0.212
dyspnea 6 (0.08%) 5 (0.07%) 0.784
vomiting 5 (0.07%) 5 (0.07%) 1.000*
body ache 4 (0.05%) 3 (0.04%) 1.000 #
palpitation 3 (0.04%) 5 (0.07%) 0.504 #
ulceration 2 (0.03%) 4 (0.06%) 0.449 #

*: Continuity correction; #: Fisher exact test