Table 3.

Treatment-related adverse events

Adverse eventAll HSCT (N = 28)Mild-moderate-severe VOD/SOS (n = 11)Very severe VOD/SOS (n = 17)
Hypotension, n (%) 3 (11) 3 (18) 
Lower gastrointestinal hemorrhage, n (%) 1 (4) 1 (6) 
Epistaxis, n (%) 5 (18) 1 (9) 4 (24) 
Grade III/IV pulmonary hemorrhage, n (%) 1 (4) 1 (6) 
Grade III/IV upper gastrointestinal hemorrhage, n (%) 1 (4) 1 (6) 
Hematuria, n (%) 12 (43) 3 (27) 9 (53) 
Adverse eventAll HSCT (N = 28)Mild-moderate-severe VOD/SOS (n = 11)Very severe VOD/SOS (n = 17)
Hypotension, n (%) 3 (11) 3 (18) 
Lower gastrointestinal hemorrhage, n (%) 1 (4) 1 (6) 
Epistaxis, n (%) 5 (18) 1 (9) 4 (24) 
Grade III/IV pulmonary hemorrhage, n (%) 1 (4) 1 (6) 
Grade III/IV upper gastrointestinal hemorrhage, n (%) 1 (4) 1 (6) 
Hematuria, n (%) 12 (43) 3 (27) 9 (53) 

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