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Table 3 Adverse Events

From: The efficacy of paritaprevir/ritonavir/ombitasvir+dasabuvir and ledipasvir/sofosbuvir is comparable in patients who failed interferon-based treatment with first generation protease inhibitors - a multicenter cohort study

Parameter

Boceprevir-experienced

Telaprevir-experienced

 

LDV/SOF

(n = 63)

PrOD

(n = 64)

LDV/SOF

(n = 105)

PrOD

(n = 103)

Patients with at least one AE, n (%)

24 (38.1%)

28 (43,8%)

44 (41.9%)

45 (43.7%)

 RBV-containing regimen

18 (28.6%)

19 (29.7%)

31 (29.5%)

33 (32%)

Most common AEs (> 5%), n (%)

 Fatigue

15 (23.8%)

17 (26.6%)

27 (25.7%)

30 (29.1%)

 Anaemia

9 (14.3%)

13 (20.3%)

15 (14.3%)

22 (21.4%)

 Headache

8 (12.7%)

11 (17.2%)

10 (9.5%)

12 (11.7%)

 Nausea

4 (6.3%)

4 (6.3%)

7 (6.7%)

8 (7.8%)

Serious AEs, n (%)

1 (1.6%)

1 (1.6%)

2 (1.9%)

1 (1%)

Deaths

1 (1.6%)

0 (0%)

2 (1.9%)

0 (0%)