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. 2012 Nov 14;2012(11):CD008079. doi: 10.1002/14651858.CD008079.pub2

Table 3.

Adverse events (reported by one trial)

Name of trial Adverse event Experimental arm (N) Control arm (N)
GCLLSG CLL 8
Cytokine release syndrome grade 3/4 1/404 0/396
Haematological toxicity grade 3/4 225/404 157/396
Leukocytopenia grade 3/4 97/404 48/396
Tumour lysis syndrome grade 3/4 1/404 2/396
Autoimmune haemolytic anaemia 22/404 27/396
Infection 103/404 85/396
REACH
Febrile neutropenia grade 3/4 33/274 32/272
Granulocytopenia grade 3/4 18/274 12/272
Hepatitis B grade 3/4 0/274 5/272
Pancytopenia grade 3/4 9/274 13/272
Pneumonia 15/274 17/272