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Distribution of adverse events per study arm among all enrolled study participants
| 1 week group | 2 week group | 4 week group | 4 week plusIPV group | Total | |
|---|---|---|---|---|---|
|
| |||||
| Mild to moderate adverse events | |||||
| Burn injury | 0 | 0 | 0 | 1 | 1 |
| Conjunctivitis | 0 | 0 | 2 | 1 | 3 |
| Diarrhoea | 2 | 0 | 0 | 2 | 4 |
| Vaccine-related fever | 1 | 0 | 0 | 2 | 3 |
| Respiratory infection | 1 | 1 | 4 | 1 | 7 |
| Oral candidiasis | 0 | 1 | 0 | 1 | 2 |
| Skin infection | 1 | 0 | 2 | 1 | 4 |
| Measles | 0 | 1 | 0 | 0 | 1 |
| Varicella | 0 | 1 | 0 | 0 | 1 |
| Serious adverse events | |||||
| Pneumonia | 1 | 0 | 1 | 0 | 2 |
| Total | 6 | 4 | 9 | 9 | 28 |
Data are n.
