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. 2015 Dec 3;10(12):e0143072. doi: 10.1371/journal.pone.0143072

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.