Table 1. Characteristics of included studies.
Author name | Year | Setting | Groups | Sample size | Dose of favipiravir | Mean age in years | Males, % | Mild cases, % | Moderate cases, % |
Bosaeed et al. [14] | 2022 | Multi-center | Favipiravir | 112 | First day: 1800 mg and 800 mg from day 2 onwards | 36.5 | 67.10% | 100% | 0% |
Control | 119 | ||||||||
Chuah et al. [15] | 2022 | Multi-center | Favipiravir | 250 | First day: 1800 mg and 800 mg from day 2 onwards | 62.5 | 48.40% | 49.80% | 50.20% |
Control | 250 | ||||||||
Holubar et al. [16] | 2022 | Single center | Favipiravir | 59 | First day: 1800 mg and 800 mg from day 2 onwards | 43.2 | 42.24% | 100% | 0% |
Control | 57 | ||||||||
Khamis et al. [17] | 2021 | Single Center | Favipiravir | 44 | First day: 1600 mg and 600 mg from day 2 onwards | 55 | 58% | NR | NR |
Control | 45 | ||||||||
Lou et al. [18] | 2020 | Single Center | Favipiravir | 9 | First day: 1600 mg and 600 mg from day 2 onwards | 52.3 | 73.70% | NR | NR |
Control | 10 | ||||||||
McMohan et al. [19] | 2022 | Single center | Favipiravir | 95 | First day: 1800 mg and 800 mg from day 2 onwards | 36 | 54.80% | NR | NR |
Control | 95 | ||||||||
Shinkai et al. [20] | 2021 | Single center | Favipiravir | 107 | First day: 1800 mg and 800 mg from day 2 onwards | 46.3 | 66.70% | 0% | 100% |
Control | 49 | ||||||||
Udwadia et al. [11] | 2021 | Multi-center | Favipiravir | 72 | First day: 1800 mg and 800 mg from day 2 onwards | 43.3 | 73.50% | 60.50% | 39.50% |
Control | 75 |