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Table 4 New signal strength at the PT level for Furosemide, torsemide, and bumetanide

From: A disproportionality analysis of adverse events associated with loop diuretics in the FDA Adverse Event Reporting System (FAERS)

Drug

Preferred Term (PT)

N

ROR (95% CI)

p

Furosemide

Vitamin b1 deficiency

65

156.59(119.63, 204.97)

<0.01

Gastrointestinal tract mucosal pigmentation

38

145.61(102.63, 206.59)

<0.01

Wernicke’s encephalopathy

41

64.48(46.82, 88.81)

<0.01

Torsemide

Palisaded neutrophilic granulomatous dermatitis

6

1592.54(645.57, 3928.58)

<0.01

Systemic infection

28

108.04(74.3, 157.1)

<0.01

Respiratory tract haemorrhage

3

31.55(10.14, 98.15)

<0.01

Coarctation of the aorta

5

31.39(13.03, 75.61)

<0.01

Haematochezia

45

5.52(4.11, 7.39)

<0.01

Haematemesis

19

4.81(3.06, 7.54)

<0.01

Haematuria

18

3.34(2.1, 5.31)

<0.01

Pemphigoid

15

14.63(8.81, 24.3)

<0.01

Toxic epidermal necrolysis (TEN)

9

3.97(2.07, 7.64)

<0.01

Prothrombin time prolonged

7

7.01(3.34, 14.72)

<0.01

Bumetanide

Blood ketone body increased

3

109.76(35.28, 341.5)

<0.01

Metabolic encephalopathy

4

34.77(13.03, 92.8)

<0.01

Lip swelling

6

4.73(2.12, 10.54)

<0.01

Stevens-Johnson syndrome (SJS)

4

4.62(1.73, 12.32)

<0.01

Pemphigoid

3

11.5(3.71, 35.71)

<0.01