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Table 2 Comparison of adverse events and serious adverse events between the low-dose and conventional-dose groups

From: Efficacy and safety of low-dose Sirolimus in Lymphangioleiomyomatosis

Type of event

Total

Low-dose

Conventional-dose

Number of patients

39

20

19

Adverse events

35 (89.7)

17 (85.0)

18 (94.7)

 Hypercholesterolaemia

17 (43.6)

7 (35.0)

10 (52.6)

 Stomatitis

14 (35.9)

10 (50.0)*

4 (21.1)

 URI

9 (23.0)

3 (15.0)

6 (31.6)

 Diarrhoea

7 (17.9)

4 (20.0)

3 (15.8)

 Headache

5 (12.8)

4 (20.0)

1 (5.3)

 Vaginal bleeding

5 (12.8)

1 (5.0)

4 (21.1)

 Acneiform lesions

4 (10.3)

3 (15.0)

1 (5.3)

 UTI

4 (10.3)

2 (10.0)

2 (10.5)

Serious adverse events

7 (17.9)

3 (15.0)

4 (21.1)

 Infectiona

4 (10.3)

3 (15.0)

1 (5.3)

 Pneumothorax

3 (7.7)

1 (5.0)

2 (10.5)

 Malignancyb

1 (2.3)

0 (0.0)

1 (5.3)

  1. Data are presented as number (%)
  2. Abbreviations: URI upper respiratory infection, UTI urinary tract infection
  3. *P < .1 (compared with conventional-dose group)
  4. aInfection included pneumonia (n = 3) and cellulitis (n = 1)
  5. bThyroid cancer