Table 2 Adverse events with everolimus plus fulvestrant.

From: Fulvestrant and everolimus efficacy after CDK4/6 inhibitor: a prospective study with circulating tumor DNA analysis

Adverse events

All grades

Grade 3 and 4

Number of patients N = 57

%

Number of patients N = 57

%

Hyperglycemia

13

22.8

0

0

Mucositis

39

68.4

6

10.5

Pneumonitis

9

15.8

1

1.8

Decreased weight

18

31.6

1

1.8

Nausea

8

14.0

0

0

Rash

18

31.6

0

0

Diarrhea

13

22.8

0

0

Constipation

6

10.5

0

0

hypercholesterolemia

16

28.1

0

0

Neutropenia

4

7.0

1

1.8

Hypertriglyceridemia

15

26.3

2

3.5

Alanine aminotransferase increased

15

26.3

0

0

Asthenia

27

47.4

0

0

Dyspnea

15

26.3

0

0