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. 2020 May 19;11:710. doi: 10.3389/fphar.2020.00710

Table 4.

Characteristics of the reported adverse events.

Adverse events Total (n = 494) SOF + RBV (n = 162) SOF/DCV ± RBV (n = 41) OBV/PTV/r/DSV ± RBV (n = 212) EBR/GZR (n = 64) DCV + ASV (n = 15)
Fatigue 47 (9.5) 15 (9.3) 8 (19.5) 21 (9.9) 2 (3.1) 1 (6.7)
Headache 14 (2.8) 4 (2.5) 2 (4.9) 8 (3.8) 0 (0) 0 (0)
Dizziness 29 (5.9) 7 (4.3) 3 (7.3) 13 (6.1) 5 (7.8) 1 (6.7)
Insomnia 14 (2.8) 5 (3.1) 4 (9.8) 2 (4.7) 2 (3.1) 1 (6.7)
Diarrhea 3 (0.6) 1 (0.6) 0 (0) 1 (0.5) 1 (1.6) 0 (0)
Nausea 11 (2.2) 2 (1.2) 1 (2.4) 5 (2.4) 2 (3.1) 1 (6.7)
Vomiting 11 (2.2) 0 (0) 1 (2.4) 7 (3.3) 3 (4.7) 0 (0)
Anemia 37 (7.5) 21 (12.9) 5 (12.2) 11 (5.2) 0 (0) 0 (0)
Abnormal liver function 24 (4.9) 8 (4.9) 3 (7.3) 10 (4.7) 1 (1.6) 2 (13.3)

Data expressed as sample size and proportion (%).

SOF, sofosbuvir; RBV, ribavirin; DCV, daclatasvir; EBR/GZR, elbasvir/grazoprevir; OBV/PTV/r/DSV, ombitasvir/paritaprevir/ritonavir and dasabuvir; ASV, asunaprevir.