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Table 4 Adverse events by preferred term, regardless of relationship to everolimus

From: Assessing the outcomes of everolimus on renal angiomyolipoma associated with tuberous sclerosis complex in China: a two years trial

n(%)

 

Everolimus (N = 18)

All grades

Grade 3

Grade 4

Grade 5

Mucositis oral

18(100%)

2(11.1%)

Irregular menstruation

11(91.7%)

3(25.0%)

Abdominal pain

14(77.8%)

1(5.6%)

Hypertriglyceridemia

13(72.2%)

Headache

12(66.7%)

Diarrhea

11(61.1%)

Upper respiratory infection

10(55.6%)

Proteinuria

9(50%)

1(5.6%)

Malaise

9(50%)

Rash acneiform

8(44.4%)

Cholesterol high

8(44.4%)

Fever

6(33.3%)

Urinary tract infection

5(27.8%)

Hematuria

5(27.8%)

Alkaline phosphatase increased

5(27.8%)

Constipation

4(22.2%)

GGT increased

4(22.2%)

Hypophosphatemia

4(22.2%)

Seizures

3(16.7%)

Pneumonitis

2(11.1%)

1(5.6%)

1(5.6%)

Vomiting

2(11.1%)

1(5.6%)

Lymphocyte count decreased

2(11.1%)

Anemia

2(11.1%)

Renal hemorrhage

1(5.6%)

1(5.6%)

Neutrophil count decreased

1(5.6%)

Hyperuricemia

1(5.6%)

Creatinine increased

1(5.6%)