Table 2.
Frequency of adverse events by time since vaccination
0–30 min |
31 min to 3 days |
4–14 days |
Overall (0–14 days) |
|||||
---|---|---|---|---|---|---|---|---|
Response rate | Frequency | Response rate | Frequency | Response rate | Frequency | Response rate | Frequency | |
Adults (≥18 years, n=1207) | ||||||||
Arthralgia | 100% | 0 | 97% | 80 (7%) | 96% | 1 (<1%) | 93% | 81 (7%) |
Diarrhoea | 100% | 0 | 97% | 3 (<1%) | 96% | 0 | 93% | 3 (<1%) |
Fatigue | 100% | 1 (<1%) | 97% | 118 (10%) | 96% | 1 (<1%) | 94% | 119 (10%) |
Fever | 100% | 0 | 97% | 1 (<1%) | 96% | 0 | 93% | 1 (<1%) |
Headache | 100% | 0 | 97% | 180 (15%) | 96% | 0 | 94% | 180 (16%) |
Induration | 100% | 0 | 97% | 1 (<1%) | 96% | 0 | 93% | 1 (<1%) |
Injection pain | 100% | 1 (<1%) | 97% | 37 (3%) | 96% | 0 | 93% | 38 (3%) |
Muscle pain | 100% | 0 | 97% | 157 (13%) | 96% | 0 | 94% | 157 (14%) |
Myalgia | 100% | 0 | 97% | 149 (13%) | 96% | 0 | 94% | 149 (13%) |
Vomiting | 100% | 0 | 97% | 2 (<1%) | 96% | 0 | 93% | 2 (<1%) |
Other adverse events | 100% | 2 (<1%) | 97% | 29 (2%) | 96% | 2 (<1%) | 93% | 33 (3%) |
Any adverse events* | 100% | 3 (<1%) | 97% | 408 (35%) | 96% | 4 (<1%) | 94% | 412 (36%) |
Children (6–17 years, n=303) | ||||||||
Arthralgia | 100% | 0 | 94% | 1 (<1%) | >99% | 0 | 93% | 1 (<1%) |
Diarrhoea | 100% | 0 | 94% | 2 (1%) | >99% | 0 | 93% | 2 (1%) |
Fatigue | 100% | 0 | 94% | 3 (1%) | >99% | 1 (<1%) | 93% | 3 (1%) |
Fever | 100% | 0 | 94% | 0 | >99% | 0 | 93% | 0 |
Headache | 100% | 0 | 94% | 33 (12%) | >99% | 1 (<1%) | 93% | 34 (12%) |
Induration | 100% | 0 | 94% | 0 | >99% | 0 | 93% | 0 |
Injection pain | 100% | 0 | 94% | 0 | >99% | 0 | 93% | 0 |
Muscle pain | 100% | 0 | 94% | 10 (4%) | >99% | 0 | 94% | 10 (4%) |
Myalgia | 100% | 0 | 94% | 9 (3%) | >99% | 0 | 94% | 9 (3%) |
Vomiting | 100% | 0 | 94% | 0 | >99% | 0 | 93% | 0 |
Other adverse events | 100% | 0 | 94% | 3 (1%) | >99% | 1 (<1%) | 93% | 4 (1%) |
Any adverse events* | 100% | 0 | 94% | 47 (17%) | >99% | 2 (1%) | 94% | 47 (17%) |
Data are % or n (%). Response rates were used to calculate the percentage of events for each line.
Response rate calculated as the proportion of individuals who answered all adverse event fields or reported at least one adverse events.