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Table 2 Most frequent (≥10% of patients) treatment-emergent adverse events of any grade in the safety population

From: Efficacy and safety of rucaparib in previously treated, locally advanced or metastatic urothelial carcinoma from a phase 2, open-label trial (ATLAS)

TEAE

Overall (N = 97)

Any grade, n (%)

Grade ≥3, n (%)

Asthenia/fatigue

56 (57.7)

8 (8.2)

Nausea

41 (42.3)

1 (1.0)

Anemiaa

35 (36.1)

20 (20.6)

Decreased appetite

28 (28.9)

2 (2.1)

Thrombocytopeniab

22 (22.7)

11 (11.3)

Vomiting

22 (22.7)

1 (1.0)

Blood creatinine increased

21 (21.6)

1 (1.0)

Constipation

21 (21.6)

3 (3.1)

ALT/AST increased

17 (17.5)

5 (5.2)

Dysgeusia

16 (16.5)

0

Dyspnea

13 (13.4)

3 (3.1)

Weight decreased

13 (13.4)

0

Diarrhea

12 (12.4)

1 (1.0)

Urinary tract infection

12 (12.4)

4 (4.1)

Abdominal pain

11 (11.3)

1 (1.0)

Hypophosphatemia

10 (10.3)

5 (5.2)

Dehydration

10 (10.3)

2 (2.1)

Insomnia

10 (10.3)

0

Pyrexia

10 (10.3)

1 (1.0)

  1. ALT alanine aminotransferase; AST aspartate aminotransferase; TEAE treatment-emergent adverse event.
  2. Visit cutoff date: February 20, 2020.
  3. a Combined term for anemia or decreased hemoglobin.
  4. b Combined term for thrombocytopenia or decreased platelets.