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Table 4 Adverse events while taking sirolimus according to the duration of treatment in patients with LAM

From: Long-term efficacy and safety of sirolimus therapy in patients with lymphangioleiomyomatosis

Time after sirolimus (years)

Number (%)

Year 1 (N = 107)

Year 2 (N = 70)

Year 3 (N = 53)

Year 4 (N = 30)

Mouth ulcer

73 (68.2)

33 (47.1)

22 (41.5)

7 (23.3)

Menstrual abnormality

62 (57.9)

34 (48.6)

16 (30.2)

8 (26.7)

Acne

37 (34.6)

22 (31.4)

12 (22.6)

3 (10.0)

Ovarian cystsa

17/55 (30.9)

10/37 (27.0)

6/25 (24.0)

1/8 (12.5)

Weakness

11 (10)

1 (1.4)

0

0

Peripheral edema

6 (5.6)

2 (2.9)

1 (1.9)

1 (3.3)

Diarrhea

6 (5.6)

1 (1.4)

0

0

Rash

5 (4.7)

0

0

1 (3.3)

Nausea

5 (4.7)

0

1 (1.9)

0

Weight loss

5 (4.7)

0

0

0

Arthralgia

4 (3.7)

0

0

1 (3.3)

Abdominal pain

3 (2.8)

2 (2.9)

0

0

Pruritus

3 (2.8)

1 (1.4)

0

0

Abdominal distention

2 (1.9)

0

0

0

Fever

2 (1.9)

0

0

0

Chest pain

2 (1.9)

1 (1.4)

1 (1.9)

1 (3.3)

Toothache

1 (0.9)

0

0

0

Gingival hyperplasia

1 (0.9)

0

0

0

Periodontitis

1 (0.9)

0

0

0

Herpes zoster

1 (0.9)

1 (1.4)

0

0

Alopecia

1 (0.9)

0

0

0

Headache

1 (0.9)

0

0

0

Dizziness

1 (0.9)

0

0

0

Palpitation

1 (0.9)

0

0

0

Myalgia

1 (0.9)

0

0

0

Tenosynovitis

1 (0.9)

0

0

0

  1. abased on patients evaluated