Table 1 Clinical characteristics of reports with Pexidartinib from the FAERS database.

From: A disproportionality analysis of adverse events caused by pexidartinib from the FDA adverse event reporting system

Characteristic

Case Number, n

Proportion, %

Total

844

 

Gender

 Female

461

54.60%

 Male

283

33.50%

 Missing

100

11.80%

Weight

 <50 kg

1

0.10%

 >100 kg

12

1.40%

 50–100 kg

79

9.40%

 Missing

752

89.10%

Age

 <18

13

1.50%

 18–64.9

222

26.30%

 65–85

28

3.30%

 Missing

581

68.80%

Reporter’s type

 Consumer

424

50.20%

 Physician

212

25.10%

 Pharmacist

17

2.00%

 Other health-professional

191

22.60%

Outcomes

 Hospitalization—initial or prolonged

62

7.30%

 Disability

3

0.40%

 Life-threatening

1

0.10%

 Death

14

1.70%

 Other serious

99

11.70%

 Non-Serious

665

78.80%

Reported countries (top five)

 America

843

99.90%

 Italy

1

0.10%