Skip to main content
. 2021 Oct 27;13(10):1215–1233. doi: 10.4254/wjh.v13.i10.1215

Table 4.

Reported effects of selected coronavirus disease 2019 therapies on liver

Medication (class)
Pattern of liver injury
Evidence
Corticosteroids (Anti-inflammatory agent) Acute liver injury[77] Multicenter cohort study (n = 774); COVID-19 with ARDS: Incidence of ALI versus control (18.3% vs 9.9%; P = 0.001)[77]
Meta-analysis; critically ill COVID-19 patients: No association with serious adverse effects[78]
RECOVERY trial: No reported serious ADRs or DILI[79]
Favipiravir (RdRp inhibitor) Abnormal LFTs[80] RCT (n = 150); mild-to-moderate COVID-19: Abnormal LFTs versus control 6.8% vs 2.7%)[80]
Elevation of transaminases levels[81] RCT; moderate COVID-19: Elevated ALT and AST were reported[81]
Hydroxychloroquine (Antimalarial agent) Liver toxicity is not common[82]. Elevation of transaminases levels[74,75,82-84] Retrospective study (n = 153): Elevation in AST (11%) and ALT (9%)[82]
RCT (n = 504); mild-to-moderate COVID-19: Elevation in ALT or AST elevation 10.6% in HCQ plus azithromycin, 9% in HCQ, and 3.5% in control arm (P = 0.008)[83]
Systematic review: Elevations of LFTs was transient[84]
Recovery trial: No reported DILI[85]
Interferon - Data on safety in COVID-19 patients is scarce
Lopinavir/ritonavir (Protease inhibitor) Rise in liver function parameters[5,27,34,74,86] RCT (n = 199): Elevated AST versus control (2.1% vs 5.1%), elevated ALT (1.1% vs 1 %), elevated TB (3.2% vs 3 %)[86]
Hyperbilirubinemia[5,34] Meta-analysis: DILI in 37.2% of patients (as hyperbilirubinemia followed by elevation of transaminases)[5]
Remdesivir (RdRp inhibitor) Not well established. Elevation of transaminases levels[5,75,87-89]. Elevation of TB levels[88]. Hypoalbuminemia[88] Case series: Elevated aminotransferases in 23 % discontinuation in 4% of patients[87]
RCT (n = 237) in severe COVID-19: Elevated TB versus placebo (10% vs 9%) and AST (5% vs 12%), hypoalbuminemia (13% vs 15%). Discontinuation in 1% of patients[88]
Open-label, phase 3 trial: Elevated ALT (5%-6%) and AST (7%-8%)[89]
Meta-analysis: Pooled incidence of DILI of 15.2%[5]
Meta-analysis: No difference as compared to placebo in liver enzymes elevation[90]
Tocilizumab (Humanized recombinant monoclonal antibody) Elevation of transaminases levels[27,75,91-94]. Liver injury as early as 24 h with a 40-fold increase in transaminases that normalized in 10 d[91] Case series; 7 severe COVID-19 patients: Up to 4.5 folds elevated baseline ALT and AST. Transaminases normalized in 3 wk[92]
Retrospective study (n = 1827): AST > 5 × ULN in 69.1%, and ALT > 5 × ULN in 72.1% of patients[75]
Observational study (n = 104): Minor increase of AST, ALT (P < 0.001) and GGT (P = 0.003; no safety concerns on follow up[93]
RCT (n = 243): ALT elevation versus placebo (5% vs 4.9%), AST elevation in 3.7%[94]
RCT (n = 130); moderate or severe COVID-19: No increase in hepatitis risk[95]

COVID-19: Coronavirus disease 2019; ADRs: Adverse drug reactions; ALI: Acute liver injury; ALT: Alanine aminotransferase; ALP: Alkaline phosphatase, ALI: Acute liver injury; ARDS: Acute respiratory distress syndrome; AST: Aspartate aminotransferase; DILI: Drug-induced liver injury; GGT: Gamma-glutamyl transpeptidase; HCQ: Hydroxychloroquine; LFTs: Liver functions tests; RCT: Randomized controlled trial; RdRp: RNA-dependent RNA polymerase; TB: Total bilirubin; ULN: Upper limit of normal.