TABLE IV.
Serious adverse events occurring in two or more patients
Event | Patient group [n(%)] | ||
---|---|---|---|
| |||
CLL (n=16) | iNHL (n=74) | Overall (n=90) | |
Any event | 6 (37.5) | 27 (36.5) | 33 (36.7) |
Pyrexia | 3 (18.8) | 6 (8.1) | 9 (10.0) |
Febrile neutropenia | 1 (6.3) | 4 (5.4) | 5 (5.6) |
Pneumonia | 0 | 3 (4.1) | 3 (3.3) |
Acute renal failure | 1 (6.3) | 2 (2.7) | 3 (3.3) |
Abdominal pain | 0 | 2 (2.7) | 2 (2.2) |
Hypotension | 1 (6.3) | 1 (1.4) | 2 (2.2) |
Nausea | 0 | 2 (2.7) | 2 (2.2) |
Pneumocystis jiroveci pneumonia | 0 | 2 (2.7) | 2 (2.2) |
Syncope | 0 | 2 (2.7) | 2 (2.2) |
Tumour lysis syndrome | 2 (12.5) | 0 | 2 (2.2) |
Vomiting | 0 | 2 (2.7) | 2 (2.2) |
CLL = chronic lymphocytic leukemia; iNHL = indolent non-Hodgkin lymphoma.