Table 4

Adverse events associated with dasatinib in the total population (n = 186) at 8-months' follow-up

Nonhematologic toxicity*All gradesGrades 3 to 4
Headache 63 (34) 2 (1) 
Diarrhea 56 (30) 4 (2) 
Fatigue 52 (28) 2 (1) 
Dyspnea 51 (27) 6 (3) 
Rash 41 (22) 1 (0.5) 
Asthenia 37 (20) 3 (2) 
Nausea 36 (19) 2 (1) 
Pleural effusion 35 (19) 6 (3) 
Peripheral edema 33 (18) 0 (0) 
Serum chemistry   
    Elevated bilirubin 26 (14) 0 (0) 
    Elevated activity of ALAT 96 (52) 3 (2) 
    Elevated activity of ASAT 111 (60) 4 (2) 
Cytopenias grade 3 to 4   
    Leukocytopenia NA 46 (25) 
    Neutropenia NA 92 (49) 
    Thrombocytopenia NA 88 (47) 
    Anemia NA 40 (22) 
Nonhematologic toxicity*All gradesGrades 3 to 4
Headache 63 (34) 2 (1) 
Diarrhea 56 (30) 4 (2) 
Fatigue 52 (28) 2 (1) 
Dyspnea 51 (27) 6 (3) 
Rash 41 (22) 1 (0.5) 
Asthenia 37 (20) 3 (2) 
Nausea 36 (19) 2 (1) 
Pleural effusion 35 (19) 6 (3) 
Peripheral edema 33 (18) 0 (0) 
Serum chemistry   
    Elevated bilirubin 26 (14) 0 (0) 
    Elevated activity of ALAT 96 (52) 3 (2) 
    Elevated activity of ASAT 111 (60) 4 (2) 
Cytopenias grade 3 to 4   
    Leukocytopenia NA 46 (25) 
    Neutropenia NA 92 (49) 
    Thrombocytopenia NA 88 (47) 
    Anemia NA 40 (22) 

Results shown as number (%).

ALAT indicates alanine aminotransferase; ASAT, aspartate aminotransferase; and NA, not applicable.

*

Nonhematologic adverse events experienced by ≥10% of patients.

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