Table 3 Summary of solicited adverse events safety population.

From: A Phase 3, randomized, non-inferiority study of a heterologous booster dose of SARS CoV-2 recombinant spike protein vaccine in adults

 

ChAdOx1 nCoV-19 Prime cohort

BBV152 Prime cohort

SII-NVX-CoV2373

(N = 92)

n (%) [E]

ChAdOx1 nCoV-19

(N = 94)

n (%) [E]

SII-NVX-CoV2373

(N = 92)

n (%) [E]

BBV152

(N = 94)

n (%) [E]

Participants with at Least One Solicited Adverse Event

33 (35.9) [69]

29 (30.9) [61]

34 (37.0) [84]

43 (45.7) [87]

Participants with at Least One Local Solicited AE

18 (19.6) [26]

24 (25.5) [28]

20 (21.7) [29]

36 (38.3) [43]

Injection Site Pain

17 (18.5) [17]

24 (25.5) [24]

20 (21.7) [20]

35 (37.2) [35]

Injection Site Tenderness

5 (5.4) [5]

3 (3.2) [3]

4 (4.3) [4]

6 (6.4) [6]

Injection Site Swelling

3 (3.3) [3]

0

3 (3.3) [3]

1 (1.1) [1]

Injection Site Erythema

1 (1.1) [1]

0

1 (1.1) [1]

0

Injection Site Induration

0

1 (1.1) [1]

1 (1.1) [1]

1 (1.1) [1]

Participants with at Least One Systematic Solicited AE

24 (26.1) [43]

17 (18.1) [33]

25 (27.2) [55]

25 (26.6) [44]

Headache

12 (13.0) [12]

11 (11.7) [11]

13 (14.1) [13]

9 (9.6) [9]

Arthralgia

7 (7.6) [7]

6 (6.4) [6]

5 (5.4) [5]

5 (5.3) [5]

Fatigue

7 (7.6) [7]

6 (6.4) [6]

11 (12.0) [11]

11 (11.7) [11]

Malaise

5 (5.4) [5]

4 (4.3) [4]

12 (13.0) [12]

7 (7.4) [7]

Myalgia

5 (5.4) [5]

3 (3.2) [3]

7 (7.6) [7]

5 (5.3) [5]

Fever

5 (5.4) [5]

0

4 (4.3) [4]

4 (4.3) [4]

Vomiting

1 (1.1) [1]

2 (2.1) [2]

1 (1.1) [1]

1 (1.1) [1]

Nausea

1 (1.1) [1]

1 (1.1) [1]

2 (2.2) [2]

2 (2.1) [2]

  1. n number of participants, E number of events.