Table 4.
Adverse events, n (%) | Neratinib a (n = 15) | Lansoprazole b (n = 15) | Neratinib + Lansoprazole c (n = 15) | Total (n = 15) |
---|---|---|---|---|
Subjects with adverse events | 4 (27) | 1 (7) | 2 (13) | 5 (33) |
Diarrhoea | 1 (7) | 0 | 2 (13) | 3 (20) |
Flatulence | 2 (13) | 0 | 0 | 2 (13) |
Abdominal pain | 1 (7) | 0 | 0 | 1 (7) |
Fatigue | 1 (7) | 0 | 0 | 1 (7) |
Dizziness | 0 | 1 (7) | 0 | 1 (7) |
Headache | 1 (7) | 0 | 0 | 1 (7) |
Note: all events were mild
Postdose on Day 1/Period 1 to predose on Day 1/Period 2
Postdose on Day 1/Period 2 to predose neratinib on Day 5/Period 2
Postdose neratinib on Day 5/Period 2 to end of study