Table 4.
Adverse events.
Adverse events | Observation group(n=29) | |
---|---|---|
Grade 1-2 AEs | ≥ Grade 3 AEs | |
Pruritus, Rash | 41.38% (12) | 3.45% (1) |
Hypertension | 34.48% (10) | 0 |
Abdominal pain, Diarrhea | 31.03% (9) | 6.90% (2) |
Fatigue | 31.03% (9) | 3.45% (1) |
Increased AST or ALT | 27.59% (8) | 0 |
Dry skin | 20.69% (6) | 3.45% (1) |
Decreased appetite | 17.24% (5) | 0 |
Stomatitis | 6.90% (2) | 0 |
AST, aspartate aminotransferase; ALT,alanine aminotransferase.