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. 2012 Feb 28;31(1):77–84. doi: 10.1007/s10637-012-9801-2

Table 2.

Treatment-related adverse eventsa

Adverse event No. (%) of patients (N = 6)
ALT increased 3 (50.0)
AST increased 2 (33.3)
Hemoglobin decreased 2 (33.3)
Decreased appetite 2 (33.3)
Epistaxis 2 (33.3)
Angina pectoris 1 (16.7)
Conjuctival hemorrhage 1 (16.7)
Eye pain 1 (16.7)
Mouth hemorrhage 1 (16.7)
Nausea 1 (16.7)
Fatigue 1 (16.7)
Pain 1 (16.7)
Liver disorder 1 (16.7)
Blood albumin decreased 1 (16.7)
Blood alkaline phosphatase increased 1 (16.7)
Blood glucose increased 1 (16.7)
Blood magnesium increased 1 (16.7)
Blood sodium increased 1 (16.7)
Platelet count decreased 1 (16.7)
WBC count decreased 1 (16.7)
Headache 1 (16.7)
Depression 1 (16.7)
Dyspnea 1 (16.7)
Pleural effusion 1 (16.7)
Hemorrhage 1 (16.7)

ALT alanine aminotransferase; AST aspartate aminotransferase; WBC white blood cell

aRelated is defined as possibly, probably, or definitely related to study drug