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. 2011 Jul 20;10:198. doi: 10.1186/1475-2875-10-198

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)