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. 2022 Mar 6;47(3):356–365. doi: 10.4093/dmj.2022.0129

Table 4.

Summarized results of the interaction effect analysis

Interaction effects BP DVT LAD PE IS TP
T2DM×(mRNA-1273) (reference: T2DM× JNJ-78436735) 1.26 (0.40–3.97) 0.80 (0.22–2.91) 1.44 (0.46–5.42) 0.58 (0.20–1.65) 1.68 (0.32–10.16) 0.15 (0.02–0.80)a
T2DM×(BNT162b2) (reference: T2DM× JNJ-78436735) 2.17 (0.67–7.08) 4.69 (1.26–18.77)a 1.67 (0.54–6.24) 2.78 (0.90–8.86) 2.54 (0.45–16.84) 0.21 (0.02–1.34)
T2DM×(mRNA-1273) (reference: T2DM× BNT162b2) 0.58 (0.31–1.07) 0.17 (0.06–0.46)b 0.87 (0.60–1.25) 0.21 (0.08–0.48)b 0.66 (0.19–2.18) 0.72 (0.17–3.08)

The odds ratio was calculated by multiple logistic regression analysis for each severe adverse event after adjusting for sex (reference: female), age, onset days, and vaccine type (reference: JNJ-78436735) as covariates. In the case of cerebral venous sinus thrombosis and encephalitis myelitis encephalomyelitis, the frequency of occurrence was very small (10 or less, respectively); therefore, the results are not presented in the table.

BP, Bell’s palsy; DVT, deep vein thrombosis; LAD, lymphadenopathy; PE, pulmonary embolism; IS, ischemic stroke; TP, thrombocytopenia; T2DM, type 2 diabetes mellitus.

a

P<0.05,

b

P<0.001.