Skip to main content

Table 9 Adverse events in each group while on ATT

From: Efficacy and safety of thrice weekly DOTS in tuberculosis patients with and without HIV co-infection: an observational study

 

HIV + (n = 150)

HIV- (n = 155)

Overall (n = 305)

Total patients experiencing adverse event(s)

69 (46.0%)

74 (47.7%)

143 (46.9%)

Total patients experiencing serious adverse event(s)

44 (29.3%)

3 (1.9%)

47 (15.4%)

IRIS*

14 (9.3%)

0

14 (4.6%)

Anaemia (new on treatment)*

9 (6.0%)

0

9 (3.0%)

Drug-induced hepatotoxicity*

5 (3.3%)

0

5 (1.6%)

Isoniazid-induced psychosis*

1 (0.7%)

0

1 (0.3%)

Stevens-Johnson syndrome*

1 (0.7%)

0

1 (0.3%)

Peripheral neuropathy*

2 (1.3%)

0

2 (0.7%)

Haemoptysis*

0

6 (3.9%)

0

Itch

9 (6.0%)

2 (1.3%)

11 (3.6%)

Rash

11 (7.3%)

2 (1.3%)

13 (4.3%)

Nausea/vomiting

47 (31.3%)

71 (45.8%)

118 (38.7%)

Diarrhoea

17 (11.3%)

24 (15.5%)

41 (13.4%)

Abdominal pain

17 (11.3%)

26 (16.8%)

43 (14.1%)

  1. * Classified as serious adverse events.