| Journal of Clinical Medicine Research, ISSN 1918-3003 print, 1918-3011 online, Open Access |
| Article copyright, the authors; Journal compilation copyright, J Clin Med Res and Elmer Press Inc |
| Journal website https://www.jocmr.org |
Review
Volume 12, Number 12, December 2020, pages 758-772
COVID-19 and Possible Pharmacological Preventive Options
Figures


Tables
| Characteristic | COVID-19 | SARS | MERS | References |
|---|---|---|---|---|
| General information on variables related to the onset and progression of COVID-19, SARS and MERS infection. COVID-19: coronavirus disease 2019; SARS-CoV-2: severe acute respiratory syndrome coronavirus 2; MERS: Middle East respiratory syndrome; WHO: the World Health Organization. | ||||
| Virus | SARS-CoV-2 | SARS-CoV | MERS-CoV | |
| First location | Wuhan, China | Guangdong, China | Jeddah, Saudi Arabia | [1, 2, 4, 5] |
| First reported | 2019 | 2002 | 2012 | [1-5] |
| Natural host | Bat | Bat | Bat | [2, 4, 5] |
| Intermediate host | Unknown | Civet cat or other animal | Dromedary camels | [2, 4, 5] |
| Incubation time (days) | 1 - 14 | 2 - 10 | 2 - 14 | WHO |
| Global incidences | 24,587,513 (to date) | 8,422 | 2,400 | WHO |
| Mode of transmission | Respiratory droplet, contact | Respiratory droplet, contact | Respiratory droplet, contact | [2, 4, 5] |
| Transmission rate | 2 - 3 | 2 - 5 | < 1 | [2, 4, 5] |
| Deaths (to date) | 833,556 | 916 | 858 | WHO |
| Mortality rate | 4% | 10% | 34% | [2, 4, 5] |
| Medication | Mode of action | References |
|---|---|---|
| Mode of action and targets of potential medical agents for the treatment of SARS-CoV-2 infection. COVID-19: coronavirus disease 2019; SARS-CoV-2: severe acute respiratory syndrome coronavirus 2; ACE2: angiotensin-converting enzyme 2; IL: interleukin; NAC: N-acetylcysteine; rhACE2: recombinant human ACE2; IFN: interferon. | ||
| Remdesivir | RNA polymerase inhibitor | [26, 27, 34] |
| Lopinavir, ritonavir | Protease inhibitor | [28] |
| Peramivir, oseltamivir | Neuraminidase/hemagglutinin-esterase inhibitor | [29] |
| Tocilizumab, anakinra, leronlimab | Cytokine receptor/cytokine release blocker | [32] |
| Camostat mesylate | ACE2 inhibitor | [33] |
| Canakinumab | human anti-IL-1β monoclonal antibody | [34] |
| rhACE2 | Recombinant ACE2 | [35] |
| Hydroxychloroquine and chloroquine | Block RNA replication/release | [33, 36, 37] |
| Azithromycin | Antibiotic/IFN production | [38] |
| Ivermectin | anti-parasitic action | [39] |
| Convalescent plasma | Anti-SARS-CoV-2 neutralizing antibodies | [40] |
| Monoclonal antibodies | block virus entry | [41] |
| Erythropoietin | Treatment of anemia | [42] |
| Enoxaparin, edoxaban | Anticoagulants | [43] |
| Vitamin C/D | Immunomodulatory, antioxidant | [45-51] |
| NAC | Antioxidant | [44] |
| Dornase alpha | DNase I | [52] |
| Medication | Status | Outcome | References |
|---|---|---|---|
| Clinical trials comparing the effect of mono- vs. combination drug therapy of COVID-19 patients. COVID-19: coronavirus disease 2019. | |||
| Hydroxychloroquine and azithromycin on mortality in patients with COVID-19 | Finalized | Reduced in-hospital mortality in patients treated with a combination treatment | [78] |
| Hydroxychloroquine and azithromycin | Finalized | Reduction in COVID-19 associated mortality | [79] |
| Interferon beta-1b, lopinavir/ritonavir, and ribavirin | Finalized | Early triple antiviral therapy was safe and superior to lopinavir/ritonavir alone in alleviating symptoms and shortening the duration | [80] |
| Remdesivir and interferon beta-1a | Ongoing | Ongoing | [81] |
| Remdesivir and tocilizumab in hospitalized participants with severe COVID-19 pneumonia (REMDACTA) | Ongoing | Ongoing | [82] |
| Intravenous immunoglobulin and remdesivir | Ongoing | Ongoing | [83] |