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. 2010 Jul 31;67(5):1119–1128. doi: 10.1007/s00280-010-1405-y

Table 2.

Number of patients with drug-related adverse events

Adverse events b.i.d. t.i.d. Total no. (%) n = 24
200 mg/m2 × 2
n = 3
400 mg/m2 × 2
n = 6
500 mg/m2 × 2
n = 3
200 mg/m2 × 3
n = 6
400 mg/m2 × 3
n = 6
G1 G2 G3 G4 G1 G2 G3 G4 G1 G2 G3 G4 G1 G2 G3 G4 G1 G2 G3 G4
Discoloration urine/stool 3 6 3 6 6 24 (100)
Blood albumin decreased 1 1 2 2 1 2 5 1 3 2 20 (83.3)
Malaise 1 1 4 3 6 3 18 (75.0)
Diarrhea 1 1 5 1 4 1 3 1 17 (70.8)
Alkaline phosphatase increased 1 6 1 2 2 1 13 (54.2)
Anorexia 2 2 1 1 2 2 1 1 12 (50.0)
Abdominal pain 2 1 2 1 2 1 2 11 (45.8)
Nauseous 1 2 1 3 1 1 9 (37.5)
Vomiting 1 2 2 3 8 (33.3)
Headache 1 2 1 1 2 7 (29.2)
Serum total protein decreased 1 1 1 1 1 1 7 (29.2)
γ-glutamyltransferase increased 1 2 1 2 6 (25.0)
Face edema 1 2 3 6 (25.0)
Back pain 1 1 1 2 5 (20.8)
Abdominal pain upper 1 1 1 2 5 (20.8)
Pleural effusion 1 1 1 1 1 5 (20.8)
Dyspnea 1 1 (4.2)
Hypoxia 1 1 (4.2)
Pericardial effusion 1 1 (4.2)
No. maximum grade 0 3 0 0 0 5 1 0 0 3 0 0 1 5 0 0 0 5 0 1

b.i.d. TSU-68 administration of twice-daily, t.i.d. TSU-68 administration of thrice-daily, G grade