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