Table 1 Overview of female adverse event reports submitted for statins in FAERS.

From: Ovary and uterus related adverse events associated with statin use: an analysis of the FDA Adverse Event Reporting System

Counting numbers by age groups (years)

Statins as a class

Atorvastatin

Simvastatin

Rosuvastatin

Pravastatin

Lovastatin

Fluvastatin

Pitavastatin

Number of AE reports (n, %)

 Overall

151,924

64,177

44,586

28,991

10,810

4,965

1,591

916

 0–18

279 (0.18%)

102 (0.16%)

74 (0.17%)

39 (0.13%)

30 (0.28%)

25 (0.50%)

5 (0.31%)

2 (0.22%)

 19–39

2,663 (1.75%)

1,034 (1.61%)

915 (2.05%)

416 (1.43%)

197 (1.82%)

87 (1.75%)

48 (3.02%)

10 (1.09%)

40–59

30,198 (19.88%)

12,287 (19.15%)

9,150 (20.52%)

6,049 (20.87%)

2096 (19.39%)

1,082 (21.79%)

372 (23.38%)

167 (18.23%)

 ≥ 60

73,777 (48.56%)

30,003 (46.75%)

22,203 (49.80%)

14,032 (48.40%)

5,618 (51.97%)

2,344 (47.21%)

800 (50.28%)

528 (57.64%)

Number of ovary and uterus related PTs with positive signals (n)

 Overall

2

6

9

2

3

2

5

0

 0–18

1

0

0

0

0

0

0

0

 19–39

3

1

2

1

1

0

0

0

 40–59

6

5

9

2

2

4

2

0

 ≥ 60

6

5

8

0

1

1

3

0

 Total number

15

12

19

3

6

5

5

0

  1. FAERS FDA Adverse Event Reporting System, AE adverse event, PTs preferred terms.