Table 3. Adverse events reported by ≥10% of patients for 12 weeks after initiation of gemcitabine.
Event, n (%) | Grade 1 | Grade 2 | Grade 3 | Grade 4 | Total, n (%) |
---|---|---|---|---|---|
Neutropenia | 3(25.0%) | 5(41.7%) | 2(16.7%) | 1(8.3%) | 11(91.7%) |
Leukopenia | 2(16.7%) | 8(66.7%) | 0 | 0 | 10(83.3%) |
Thrombocytopenia | 5(41.7%) | 1(8.3%) | 0 | 0 | 6(50.0%) |
Infection | 0 | 3(25.0%) | 2(16.7%) | 0 | 5(41.7%) |
Hb decrease | 2(16.7%) | 2(16.7%) | 0 | 0 | 4(33.3%) |
Hypoalbuminemia | 3(25.0%) | 1(8.3%) | 0 | 0 | 4(33.3%) |
Fatigue | 3(25.0%) | 1(8.3%) | 0 | 0 | 4(33.3%) |
ALT increase | 4(33.3%) | 0 | 0 | 0 | 4(33.3%) |
AST increase | 2(16.7%) | 1(8.3%) | 0 | 0 | 3(25.0%) |
Oral mucositis | 2(16.7%) | 0 | 0 | 0 | 2(16.7%) |
GGT increase | 2(16.7%) | 0 | 0 | 0 | 2(16.7%) |
ALP increase | 2(16.7%) | 0 | 0 | 0 | 2(16.7%) |
Anorexia | 2(16.7%) | 0 | 0 | 0 | 2(16.7%) |
Abbreviations: ALP, alkaline phosphatase; ALT, alanine aminotransferase; AST, aspartate aminotransferase; GGT, gamma-glutamyl transferase; Hb, hemoglobin.