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. 2013 Mar 21;13:136. doi: 10.1186/1471-2407-13-136

Table 2.

All-grade AEs occurring in ≥ 10% of patients and corresponding grades 3 and 4 AEs

 
Everolimus 10 mg/day (n = 64)
AE, n (%) All-grade Grade 3 Grade 4
Anemia
41 (64)
10 (16)
3 (5)
Hypertriglyceridemia
35 (55)
4 (6)
0 (0)
Mouth ulceration
34 (53)
2 (3)
0 (0)
Hyperglycemia
33 (52)
8 (13)
0 (0)
Hypercholesterolemia
32 (50)
0 (0)
0 (0)
Pyrexia
26 (41)
1 (2)
0 (0)
Increased blood lactate dehydrogenase
24 (38)
1 (2)
1 (2)
Fatigue
20 (31)
1 (2)
0 (0)
Increased gamma-glutamyltransferase
20 (31)
7 (11)
0 (0)
Rash
20 (31)
0 (0)
0 (0)
Increased blood creatinine
19 (30)
0 (0)
1 (2)
Cough
18 (28)
0 (0)
0 (0)
Increased aspartate aminotransferase
17 (27)
0 (0)
0 (0)
Increased alanine aminotransferase
15 (23)
1 (2)
0 (0)
Epistaxis
15 (23)
1 (2)
0 (0)
Hypocalcemia
14 (22)
0 (0)
0 (0)
Interstitial lung disease
14 (22)
1 (2)
0 (0)
Leukopenia
14 (22)
0 (0)
0 (0)
Pruritus
14 (22)
0 (0)
0 (0)
Peripheral edema
13 (20)
2 (3)
0 (0)
Decreased platelet count
13 (20)
1 (2)
0 (0)
Diarrhea
12 (19)
1 (2)
0 (0)
Dyspnea
12 (19)
1 (2)
4 (6)
Increased blood alkaline phosphatase
11 (17)
1 (2)
0 (0)
Hypokalemia
11 (17)
0 (0)
3 (5)
Lymphopenia
10 (16)
4 (6)
0 (0)
Nasopharyngitis
9 (14)
0 (0)
0 (0)
Dizziness
8 (13)
0 (0)
0 (0)
Insomnia
8 (13)
0 (0)
0 (0)
Increased blood creatine phosphokinase
7 (11)
0 (0)
0 (0)
Decreased appetite
7 (11)
1 (2)
0 (0)
Decreased hemoglobin
7 (11)
2 (3)
0 (0)
Hyponatremia
7 (11)
5 (8)
0 (0)
Nausea
7 (11)
0 (0)
0 (0)
Upper respiratory tract infection
7 (11)
0 (0)
0 (0)
Increased white blood cell count 7 (11) 0 (0) 0 (0)

AE, adverse event.