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Table 3 Characteristics of the discontinued cases, categorized into events

From: Interstitial pneumonia and other adverse events in riluzole-administered amyotrophic lateral sclerosis patients: a retrospective observational study

The reason of discontinuation of riluzole

n (rate vs. all, %)

Sex (Male, %)

Onset of ALS

Duration from the beginning of riluzole (days, median, IQR)

Duration of ALS at withdrew riluzole (years, median, IQR)

Past histories (n)

Age (years old, median, IQR)

Elevated liver enzymes

5 (5.4)

80

65 (56–67)

11 (7.3–14)

1 (1–2)

Diabetes/HT/HL (4), Reflux esophagitis (1), Heavy drinker (1)

IP

4 (4.3)

50

65.5 (55–73.3)

60 (48.5–82.5)

2 (1.8–2.5)

past smoker (2)

Appetite loss / Nausea

3 (3.3)

33

64 (62–71)

2 (2–5.5)

3 (2–4)

Depressive status (2)

Dizziness

2 (2.2)

50

69 (66–72)

4 and 90–120, respectively

2 and 20 years, respectively

 

General malaise

1 (1.1)

0

67

90

3

 

Paresthesia of tongue

1 (1.1)

100

53

180

1

Psoriasis vulgaris

Urinary urgency

1 (1.1)

100

70

0–3

2

 
  1. The most frequent cause of discontinuation was elevation of liver enzymes (n = 5/92, 5.4%) followed by IP, nausea or appetite loss, dizziness, general malaise, tongue paresthesia, or urinary urgency. In two cases, the drug was discontinued because of progression of bulbar palsy. Median disease duration was 2 years (IQR, 1–3; range, 0–20). All adverse events occurred within 6 months of riluzole initiation, with half of the events occurring within 14 days