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. 2021 Sep 23;14(10):955. doi: 10.3390/ph14100955

Table 3.

The summary of available drugs for the treatment of moderate-to-severe COVID-19.

Drugs Possible Mechanisms Indications for the Treatment of COVID-19 Routes of Administration Recommended Dosage Related Adverse Events
Remdesivir Nucleotide analogue; inhibit viral nucleotide synthesis to stop viral replication. Approved by the US FDA in hospitalized patients aged ≥12 years and weighing ≥40 kg; granted an EUA by the US FDA in hospitalized patients aged <12 years and weighing ≥3.5 kg. Intravenous. A single loading dose of 200 mg followed by once-daily maintenance doses of 100 mg for 5 to 10 days or until hospital discharge. Alterations in liver function studies, increased serum levels of creatinine, atrioventricular block, and anaphylaxis.
Baricitinib JAK inhibitor; blocks JAK-STAT signaling pathway and inflammatory response. Granted an EUA by the US FDA in combination with remdesivir in hospitalized patients aged ≥2 years requiring supplemental oxygen, invasive mechanical ventilation, or extracorporeal membrane oxygenation. Oral. 4 mg in patients aged over 9 years and 2 mg aged under 9 years once daily for 14 days or until hospital discharge. Thromboembolism, secondary infections, and hypersensitivity reaction.
Tocilizumab IL-6 receptor antagonist; inhibit IL-6 signaling pathway. Granted an EUA by the US FDA in hospitalized patients aged ≥2 years receiving systemic corticosteroids and requiring supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation. Intravenous. First dose: a single loading dose of 8 mg/kg in patients over 30 kg, and 12 mg/kg in patients under 30 kg (max. 800 mg).
Second dose: another single loading dose at least 8 h later if not improved.
Alteration in liver function studies, neutropenia, secondary infections, and allergic reactions.
Sarilumab IL-6 receptor antagonist; inhibit IL-6 signaling pathway. Under investigational use. Subcutaneous or intravenous. A single loading dose of 200 mg subcutaneously or 200 to 800 mg intravenously. Alteration in liver function studies, neutropenia, secondary infection, and allergic reaction.

Abbreviations: COVID-19, coronavirus disease 2019; EUA, Emergency Use Authorization; IL-6, Interleukin-6; JAK, Janus kinase; STAT, signal transducer and activator of transcription; US FDA, U.S. Food and Drug Administration.