Table 4.
Adverse events.
| Adverse events (n, %) | All patients (n = 35) | rhTPO group (n = 20) | Non-rhTPO group (n = 15) | p-value |
|---|---|---|---|---|
| Infection rate | 4 (11.4%) | 2 (10.0%) | 2 (13.3%) | 0.980 |
| Drug-related liver injury | 5 (14.3%) | 3 (15.0%) | 2 (13.3%) | 0.991 |
| Drug-related renal injury | 2 (5.7%) | 1 (5.0%) | 1 (6.7%) | 0.979 |
| Fatigue | 3 (8.6%) | 2 (10.0%) | 1 (6.7%) | 0.809 |
| Gastrointestinal disorders (diarrhea, nausea, and abdominal pain) | 7 (20.0%) | 4 (20.0%) | 3 (20%) | 1.000 |
| Intracranial hemorrhage | 1 (2.6%) | 1 (5.0%) | 0 (0%) | 0.999 |
rhTPO, recombinant human thrombopoietin.