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. 2024 Aug 20;15:1437267. doi: 10.3389/fimmu.2024.1437267

Table 5.

Reported vaccine-related adverse events by the groups among participants.

Adverse events SARS-CoV-2 + IIV4/PPV23 group N=203 SARS-CoV-2 + PPV23/IIV4 group N=206 SARS-CoV-2/IIV4+PPV23 group N=203 P value
n (%) n (%) n (%)
TOTAL 30(14.78) 28(13.59) 32(15.76) 0.834
Solicited adverse reactions 29(14.29) 27(13.11) 29(14.29) 0.925
Systematic 8(3.94) 7(3.40) 11(5.42) 0.594
 Fever 3(1.48) 2(0.97) 1(0.49) 0.707
 Cough 1(0.49) 2(0.97) 3(1.48) 0.707
 Headache 2(0.99) 0(0.00) 5(2.46) 0.038
 Nausea 2(0.99) 0(0.00) 1(0.49) 0.329
 Fatigue 4(1.97) 5(2.43) 5(2.46) 1.000
 Myalgia 2(0.99) 2(0.97) 7(3.45) 0.116
 Diarrhea 0(0.00) 1(0.49) 2(0.99) 0.551
 Myalgia 0(0.00) 0(0.00) 2(0.99) 0.219
Local 24(11.82) 24(11.65) 26(12.81) 0.951
 Pain 24(11.82) 21(10.19) 24(11.82) 0.829
 Rash 0(0.00) 1(0.49) 0(0.00) 1.000
 Pain 0(0.00) 3(1.46) 1(0.49) 0.331
 Induration 2(0.99) 9(4.37) 6(2.96) 0.111
Unsolicited adverse reactions 9(4.43) 5(2.43) 10(4.93) 0.360
Systematic 0(0.00) 0(0.00) 1(0.49) 0.663
 Fatigue 0(0.00) 0(0.00) 1(0.49) 0.663
 Myalgia 0(0.00) 0(0.00) 1(0.49) 0.663
Local 0(0.00) 1(0.49) 0(0.00) 1.000
 Pain 0(0.00) 1(0.49) 0(0.00) 1.000
Others 9(4.43) 4(1.94) 9(4.43) 0.305