Table 2. TEAEs occurring in ≥5% of patients (N=28).
| AEs | n (%) | |
| All grades | Grade 3 | |
| TEAE, treatment-emergent adverse events. No grade 4 and 5 adverse events occurred. | ||
| Diarrhea | 24 (85.7) | 11 (39.3) |
| Vomiting | 8 (28.6) | 1 (3.6) |
| Nausea | 7 (25.0) | 0 (0) |
| Decreased appetite | 5 (17.9) | 0 (0) |
| Upper respiratory tract infections | 4 (14.3) | 0 (0) |
| Dizziness | 4 (14.3) | 0 (0) |
| White blood cell count low | 3 (10.7) | 0 (0) |
| Cough | 3 (10.7) | 0 (0) |
| Abdominal pain | 3 (10.7) | 0 (0) |
| Dyspepsia | 3 (10.7) | 0 (0) |
| Pain in extremity | 2 (7.1) | 0 (0) |
| ALT increased | 2 (7.1) | 0 (0) |
| Fatigue | 2 (7.1) | 0 (0) |
| Hypertension | 2 (7.1) | 0 (0) |
| Skin itchiness | 2 (7.1) | 0 (0) |
| Rash | 2 (7.1) | 0 (0) |
| Headache | 2 (7.1) | 0 (0) |
| Anorexia | 2 (7.1) | 0 (0) |