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. 2020 Mar 2;16(10):2456–2464. doi: 10.1080/21645515.2020.1727697

Table 3.

Percentages of subjects experiencing mild to moderate (and severe) solicited systemic adverse events within 14 days of vaccination (safety analysis set)

  Percentages of subjects in each group with solicited systemic adverse events (severe in parentheses)
  Group A
Shantha Liquid
1 Dose
(n = 197)
Group B
Shantha Liquid
2 Doses
(n = 97)
Group A + B
Shantha Liquid
1 or 2 Doses
(n = 294)
Group C
IDT Liquid
2 Doses
(n = 100)
Group D
IDT Lyophilized
2 Doses
(n = 602)
  Dose 1 Placebo Dose 1 Dose 2 Dose 1 Dose 2 Dose 1 Dose 2 Dose 1 Dose 2
Headache 31.4
(3.1)
16.8
(3.2)
30.5
(5.3)
21.7
(2.4)
31.1
(3.8)
18.5
(2.9)
29.6
(1.0)
18.0
(3.4)
32.8
(1.9)
20.0
(2.9)
Asthenia 20.4
(2.1)
9.7
(1.3)
20.0
(0)
10.8
(1.2)
20.3.
(1.4)
10.1
(1.3)
18.4
(1.0)
13.5
(1.1)
19.6
(2.1)
10.8
(0.6)
Malaise 21.5
(3.7)
12.9
(1.3)
7.4
(0)
10.8
(1.2)
21.3
(2.8)
12.2
(1.3)
16.3
(1.0)
13.5
(2.2)
19.1
(1.7)
11.8
(1.0)
Myalgia 23.0
(1.0)
14.2
(1.3)
31.6
(2.1)
18.1
(2.4)
25.9
(1.4)
15.5
(1.7)
22.4
(2.0)
18.0
(0)
25.8
(1.0)
15.7
(0.4)
Fever 1.6
(0)
0
(0)
1.1
(0)
2.4
(0)
1.4
(0)
0.8
(0)
1.0
(0)
0
(0)
1.4
(0)
0.4
(0)

Severe fever described as body temperature >39.0ºC. Severe headache, asthenia, malaise, and myalgia all described as that preventing normal activity.