Skip to main content

Table 3 Use of specific second-line anti-TB or antiretroviral medicines and the risk of moderate-to-severe adverse events

From: Occurrence and clinical management of moderate-to-severe adverse events during drug-resistant tuberculosis treatment: a retrospective cohort study

Anti-TB medicine

Number (%) treated with the medicine, N = 57

Univariate risk ratios

95% confidence interval

p-value

Amikacin

21 (36.8%)

1.5

0.8 – 2.6

0.18

Amoxicillin/Clavulanate

1 (1.8%)

0.0

-

0.36

Capreomycin

4 (7%)

1.1

0.4 – 3.1

0.86

Ciprofloxacin

19 (33.3%)

1.5

0.8 – 2.5

0.19

Clofazimine

1 (1.8%)

0

-

0.36

Cycloserine

27 (47.4%)

0.8

0.5 – 1.5

0.49

Ethambutol

35 (61.4%)

1.7

0.9 – 3.4

0.10

Ethionamide

52 (91.2%)

0.7

0.3 – 1.6

0.50

Isoniazid

4 (7%)

1.1

0.4 – 3.1

0.86

Kanamycin

30 (52.6%)

0.8

0.4 – 1.4

0.37

Levofloxacin

37 (64.9%)

0.6

0.4 – 1.1

0.11

Para aminosalicylic acid (PAS)

5 (8.8%)

1.4

0.6 – 2.9

0.50

Pyrazinamide

53 (93%)

0.9

0.3 – 2.5

0.86

Rifampicin

13 (22.8%)

0.8

0.4 – 1.7

0.56

Streptomycin

3 (5.3%)

0.7

0.1 – 3.6

0.66

Any HAART regimen

13 (22.8%)

0.8

0.4 – 1.7

0.56

Zidovudine (AZT)

5 (8.8%)

0.4

0.1 – 2.5

0.23

Stavudine (d4T)

6 (10.5%)

1.1

0.5 – 2.6

0.82

Efavirenz (EFV)

10 (17.5%)

0.9

0.4 – 1.9

0.70

Nevirapine (NVP)

3 (5.3%)

0.7

0.1 – 3.7

0.66