Table 3. Grade ≥3 TEAEs and serious TEAEs with ≥10% incidence.
Adverse events | Niraparib 300 mg (n=20) | |
---|---|---|
Grade ≥3 TEAEs | 17 (85.0) | |
Anemia | 11 (55.0) | |
Platelet count decreased | 6 (30.0) | |
Neutrophil count decreased | 4 (20.0) | |
Lymphocyte count decreased | 2 (10.0) | |
Weight decreased | 2 (10.0) | |
White blood cell count decreased | 2 (10.0) | |
Serious TEAEs observed in ≥10% of patients | 8 (40.0) | |
Anemia | 2 (10.0) | |
Platelet count decreased | 2 (10.0) |
Values are presented as number (%) of patients. TEAEs were defined as adverse events that occurred after administration of the first dose of study drug and are shown by MedDRA Preferred Term.
MedDRA, Medical Dictionary for Regulatory Activities; TEAE, treatment-emergent adverse event.