Table 3 Adverse events recorded during the study
Adverse events | DP (n, %) | AL (n, %) | Total (n, %) |
|---|---|---|---|
Abdominal pain | 9 (4.6) | 9 (4.8) | 18 (4.7) |
Dizziness | 5 (2.5) | 2 (1.1) | 7 (1.8) |
Diarrhoea | 4 (2) | 2 (1.1) | 6 (1.6) |
Vomiting | 4 (2) | 0 (0) | 4 (1) |
Pruritus | 3 (1.5) | 1 (0.5) | 4 (1) |
Nausea | 2 (1) | 2 (1.1) | 4 (1) |
Face oedema | 1 (0.5) | 0 (0) | 1 (0.3) |
Sleepiness | 1 (0.5) | 0 (0) | 1 (0.3) |
Insomnia | 0 (0) | 1 (0.5) | 1 (0.3) |