Table 3.
Treatment-emergent adverse events reported in at least 20% of patients
| Adverse event | All patients (N = 29)
|
||||
|---|---|---|---|---|---|
| Grade 1 n (%) | Grade 2 n (%) | Grade 3 n (%) | Grade 4 n (%) | All Grades n (%) | |
| Any | 4 (14) | 11 (38) | 11 (38) | 3 (10) | 29 (100) |
| Fatigue | 10 (35) | 3 (10) | 1 (3) | 0 (0) | 14 (48) |
| Nausea | 11 (38) | 3 (10) | 0 (0) | 0 (0) | 14 (48) |
| Diarrhea | 7 (24) | 3 (10) | 0 (0) | 0 (0) | 10 (35) |
| Cough | 8 (28) | 0 (0) | 0 (0) | 0 (0) | 8 (28) |
| Dyspnea | 6 (21) | 0 (0) | 1 (3) | 1 (3) | 8 (28) |
| Hypoesthesia | 5 (17) | 3 (10) | 0 (0) | 0 (0) | 8 (28) |
| Pyrexia | 5 (17) | 3 (10) | 0 (0) | 0 (0) | 8 (28) |
| Headache | 7 (24) | 0 (0) | 0 (0) | 0 (0) | 7 (24) |
| Peripheral edema | 7 (24) | 0 (0) | 0 (0) | 0 (0) | 7 (24) |
| Constipation | 5 (17) | 1 (3) | 0 (0) | 0 (0) | 6 (21) |
| Exertional dyspnea | 6 (21) | 0 (0) | 0 (0) | 0 (0) | 6 (21) |
| Paresthesia | 4 (14) | 2 (7) | 0 (0) | 0 (0) | 6 (21) |