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Adverse events during the follow-up period (>10%).
| Adverse Events | Any Grade (%) | Grade ≥ 3 (%) |
|---|---|---|
| Hypertension | 17 (42.5%) | 3 (7.5%) |
| Proteinuria | 16 (40.0%) | 6 (15.0%) |
| Edema | 15 (37.5%) | 1 (2.5%) |
| Fever | 13 (32.5%) | - |
| Fatigue | 11 (27.5%) | - |
| Pruritus | 10 (25.0%) | - |
| Decreased appetite | 7 (17.5%) | 1 (2.5%) |
| Hand-foot skin reaction | 5 (12.5%) | - |
| Nasal bleeding | 5 (12.5%) | 1 (2.5%) |
| Rash | 4 (10.0%) | - |
| Thyroid function abnormality | 4 (10.0%) | - |
| Stomatitis | 4 (10.0%) | - |
