Copyright
©The Author(s) 2021.
World J Hepatol. Dec 27, 2021; 13(12): 1850-1874
Published online Dec 27, 2021. doi: 10.4254/wjh.v13.i12.1850
Published online Dec 27, 2021. doi: 10.4254/wjh.v13.i12.1850
Ref. | Dosage | n | Age, yr | Gender, male (%) | Incidence of adverse events in treatment vs control arm, n (%) | ||||||
Diarrhea | Vomiting | Abdominal pain | Constipation | Increased AST | Increased ALT | Drug termination due to AE | |||||
Lopinavir/ritonavir | |||||||||||
Cao et al[31] | 400/100 mg twice a day for 14 d | Tx 99; control 100 | Median 58 (IQR 49-68) | 120 (60.3) | 4 (4.2) vs 0 | 6 (6.3) vs 0 | 4 (4.2) vs 2 (2.1) | NA | 2 (2.1) vs 5 (5.1) | 1 (1.1) vs 4 (4.0) | 14% |
Li et al[32] | 200/50 mg, twice a day for 7-14 d | Tx 34; control 17 | mean ± SD, 49.4 ± 14.7 | 40 (46.5) | 9/34 (26.5) vs 0 | NA | NA | NA | NA | 1/21 (4.8) vs 0 | 1/34 (2.94) |
Remdesivir | |||||||||||
Beigel et al[50] | 200 mg daily on day 1, followed by 100 mg daily on day 2-10 | Tx 538; control 521 | mean ± SD, 58.9 ± 15.0 | 684 (64.3) | NA | NA | NA | NA | 15 (2.8) vs 20 (3.8) | 8 (1.5) vs 9 (1.7) | 49 (9.1) |
Wang et al[51] | 200 mg daily on day 1, followed by 100 mg daily on day 2-10 | Tx 158; control 79 | Median (IQR) 65 (56-71) | 89 (56) | 5 (3) vs 2 (3) | 4 (3) vs 2 (3%) | NA | 21 (14) vs 12 (15) | 7 (5) vs 9 (12) | NA | 18 (12) |
Spinner et al[53] | 200 mg daily on day 1, followed by 100 mg daily on day 2-5 or day 2-10 | 193; 193; 200 | Median (IQR) 56 (45-66) | 118 (61), 114 (60) | 5% vs 6% vs 7% | NA | NA | NA | 32 vs 32 vs 33 | 32 vs 34 vs 39 | 31 (7.8) |
Hydroxychloroquine | |||||||||||
Cavalcanti et al[70] | 400 mg daily | Tx 221; control 227 | mean ± SD, 50.3 ± 14.6 | 388 (55.3) | NA | 0 vs 1 (0.6) | NA | NA | 17 (8.5) vs 6 (3.4) | NA | NA |
Boulware et al[71] | 800 mg once, followed by 600 mg | Tx 414; control 407 | Median (IQR) 41 (33-51) | 196 (47.3) | 81 (23.2) vs 15 (4.3) for diarrhoea or abdominal pain or vomiting | 81 (23.2) vs 15 (4.3) for diarrhoea or abdominal pain or vomiting | 81 (23.2) vs 15 (4.3) for diarrhoea or abdominal pain or vomiting | NA | NA | NA | 17 (4.1) |
Favipiravir | |||||||||||
Chen et al[80] | 1600 mg twice a day on day 1, followed by 600 mg twice daily on day 2-10 | Tx 116; control 120 | NA | 59 (50.86) | NA | NA | NA | NA | 10 (8.62) | NA | Nil |
Nitazoxanide | |||||||||||
Rocco et al[82] | 500 mg 3 times per day | Tx 194; control 198 | 18-77 | 101 (52) | 57 (29.4) vs 49 (24.7) | 9 (4.6) vs 3 (1.5) | 10 (5.2) vs 5 (2.5) | NA | NA | NA | Nil |
Tocilizumab | |||||||||||
Stone et al[120] | Tocilizumab 8 mg/kg IV inf not to exceed 800 mg | Tx 161; control 82 | Median (IQR) 61.6 (46.4-69.7) | 96 (60) | NA | NA | NA | NA | 6 (3.7) vs 3 (3.7) for grade 3 or 4 | 8 (5.0) vs 4 (4.9) for grade 3 or 4 | NA |
Drug name | Gastrointestinal and hepatic side effects |
Remdesivir | Elevation of liver enzymes |
Lopinavir-ritonavir | Nausea, vomiting, abdominal pain, gastroenteritis |
Hydroxychloroquine/chloroquine | Nausea, vomiting, abdominal pain, diarrhea |
Steroids | Epigastric pain, peptic ulcer, risk of HBV reactivation |
Interferon | Diarrhea, nausea, elevated alanine aminotransferase level |
Ribavirin | Elevated liver enzyme levels |
Umifenovir | Nausea, vomiting and deranged liver function |
Bromhexine | Deranged liver function |
Favipiravir | Diarrhoea, liver enzyme abnormalities |
Nitazoxanide | Nausea, vomiting, diarrhoea and abdominal pain |
Imervectin | Elevation of liver enzymes |
Molnupiravir | Elevated alanine aminotransferase |
Tocilizumab | Liver dysfunction |
Baricitinib | Nausea, liver dysfunction |
Azithromycin | Nausea, vomiting |
Vaccine | Mechanism | Number of participants | Efficacy |
mRNA-1273 (Moderna)[125] | RNA (embedded in lipid nanoparticles)encodes a variant of the SARS-CoV-2 spike protein | 30420 participants (randomized 1:1 vaccine vs placebo) | Efficacy 94.1% (11 vaccinated vs 185 controls with COVID-19) |
BNT162b2 (BioNTech and Pfizer)[124] | RNA (embedded in lipid nanoparticles) encodes a variant of the SARS-CoV-2 spike protein | 43548 participants (randomized 1:1 vaccine vs placebo) | Efficacy 95% (9 vaccinated vs 169 controls with COVID-19) |
ChAdOx1 nCoV-19 (AZD122; AstraZenenca and University of Oxford)[126] | Replication-deficient chimpanzee adenovirus vector, containing the full-length codon-optimized coding sequence of SARS-CoV-2 spike protein | 23848 participants (randomized 1:1 vaccine vs placebo) | Efficacy 70.4% [30 (0.5%) of 5807 vaccine recipients vs 101 (1.7%) of 5829 controls with COVID-19] |
CoronaVac (Sinovac Life Sciences, Beijing, China)[129,131] | Inactivated vaccine candidate against COVID-19 | 600 participants | Seroconversion was seen in 114 (97%) of 117 in the 3 μg group, 118 (100%) of 118 in the 6 μg group, and none (0%) of 59 in the placebo group |
Sinopharm vaccine[132] | Inactivated vaccine candidate against COVID-19 | 448 participants | Neutralizing antibodies were detected in 100% of recipients |
- Citation: Law MF, Ho R, Law KWT, Cheung CKM. Gastrointestinal and hepatic side effects of potential treatment for COVID-19 and vaccination in patients with chronic liver diseases. World J Hepatol 2021; 13(12): 1850-1874
- URL: https://www.wjgnet.com/1948-5182/full/v13/i12/1850.htm
- DOI: https://dx.doi.org/10.4254/wjh.v13.i12.1850