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. 2022 Feb 9;3(4):e274–e283. doi: 10.1016/S2666-5247(21)00305-0

Table 4.

Solicited vaccination reactions after a booster dose of BNT162b2 after the initial receipt of a complete CoronaVac regimen

Age <60 years (n=28) Age ≥60 years (n=42) All (N=70*)
Any reaction 25 (89·3%) 31 (73·8%) 56 (80·0%)
Local reaction 24 (85·7%) 27 (64·3%) 51 (72·9%)
Pain 24 (85·7%) 25 (59·5%) 49 (70·0%)
Induration 6 (21·4%) 9 (21·4%) 15 (21·4%)
Redness 0 3 (7·1%) 3 (4·3%)
Systemic reaction 17 (60·7%) 12 (28·6%) 29 (41·4%)
Malaise 12 (42·9%) 7 (16·7%) 19 (27·1%)
Headache 12 (42·9%) 7 (16·7%) 19 (27·1%)
Myalgia 9 (32·1%) 0 9 (12·9%)
Joint pain 10 (35·7%) 0 10 (14·3%)
Fever and shivering 7 (25·0%) 0 7 (10·0%)
Shivering 3 (10·7%) 0 3 (4·3%)
Fever 6 (21·4%) 0 6 (8·6%)
Nausea 3 (10·7%) 0 3 (4·3%)
Vomiting 1 (3·6%) 0 1 (1·4%)
Dizziness 4 (14·3%) 0 4 (5·7%)
Diarrhoea 0 0 0
Stomach-ache 2 (7·1%) 0 2 (2·9%)

Data presented as n (%).

*

Of the 85 participants evaluated in this group, 70 responded to the survey after the booster dose.