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. 2022 May 12;10:877232. doi: 10.3389/fpubh.2022.877232

Table 4.

Multivariate logistic regression analyses showing adverse effects associated to the vaccine brand received by the physical therapists who participated in the study.

Adverse effects AZ (n = 406) PB (n = 141) OR (95% CI) p Mo (n = 34) OR (95% CI) p
Pain at the place where the vaccine was administered
   Yes 330 (81.3) 112 (79.4) 1.61 (0.77–3.36) 0.203 29 (85.3) 0.93 (0.30–2.90) 0.894
Fever
   Yes 231 (56.9) 44 (31.2) 0.67 (0.40–1.13) 0.132 15 (44.1) 1.43 (0.60–3.40) 0.421
Headache
   Yes 219 (53.9) 42 (29.8) 0.49 (0.31–0.77) 0.002* 13 (38.2) 0.69 (0.32–1.50) 0.351
Vomiting
   Yes 28 (6.9) 2 (1.4) 0.48 (0.11–2.13) 0.332 1 (2.9) 1.22 (0.14–10.5) 0.858
Tiredness
   Yes 264 (65.0) 82 (58.2) 1.48 (0.89–2.44) 0.129 18 (52.9) 0.92 (0.42–2.05) 0.844
Shivering
   Yes 208 (51.2) 29 (20.6) 0.34 (0.20–0.58) <0.001* 8 (23.5) 0.32 (0.12–0.82) 0.017*
Generalized muscle pain
   Yes 212 (52.2) 50 (35.5) 0.90 (0.54–1.49) 0.678 6 (17.6) 0.23 (0.08–0.62) 0.004*
Inflammation of the ganglia
   Yes 36 (8.9) 6 (4.3) 0.56 (0.22–1.44) 0.229 5 (14.7) 0.12 (0.01–1.22) 0.353

Data shown as n (percent within the vaccine brand). OR = calculated for each answer as compared to all the others; p = calculated for the Chi-square test group. The negative response to the presence of the adverse effect was taken as the reference value for the multivariate logistic regression analysis. AZ, AstraZeneca-Oxford; PB, Pfizer-BioNTech. Mo, Moderna.

*

p <0.05 Chi-square calculated as contingency table.