Table 5.
Summary of most frequently reported drug-related clinical adverse events* (≥10% of subjects)
| APL N = 24 | LPV/r N = 23 | APL + LPV/r N = 22 | |
|---|---|---|---|
| Any event | 12/24 (50%) | 11/23 (48%) | 11/22 (50%) |
| Gastrointestinal | |||
| Loose stools | 11/24 (46%) | 4/23 (17%) | 5/23 (23%) |
| Nausea | 5/24 (21%) | 4/23 (17%) | 7/22 (32%) |
| Abdominal pain | 1/24 (4%) | 4/23 (17%) | 1/22 (5%) |
| Vomiting | 0/24 (0%) | 0/23 (0%) | 3/22 (14%) |
| Diarrhoea | 1/24 (4%) | 4/23 (17%) | 0/22 (0%) |
| Metabolism and nutrition | |||
| Anorexia | 0/24 (0%) | 0/23 (0%) | 4/22 (18%) |
All adverse events classified as grade 1. APL, Aplaviroc; LPV, lopinavir.