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Pharmacological basis for the potential role of Azithromycin and Doxycycline in management of COVID-19. | LitMetric

AI Article Synopsis

  • A novel coronavirus, SARS-CoV-2, causes COVID-19, leading to complications like viral pneumonia and secondary infections, necessitating the use of antibiotics.
  • The review highlights the dual effects of azithromycin (AZ) and doxycycline (DOX), detailing their antiviral properties and safety concerns based on current clinical trials.
  • AZ shows effective lung tissue access and antibacterial efficacy, but raises cardiovascular risk worries, while DOX is considered safer with good lung access and potential for immune modulation.

Article Abstract

A novel corona virus SARS-CoV-2 has led to an outbreak of the highly infectious pandemic COVID-19 complicated viral pneumonia. Patients with risk factors frequently develop secondary infections where the role of appropriate antibiotics is mandatory. However, the efforts of drug repurposing lead to recognizing the role of certain antibiotics beyond the management of infection. The current review provided the detailed antiviral, immunomodulatory effect, unique pharmacokinetic profile of two antibiotics namely azithromycin (AZ) and doxycycline (DOX). It summarizes current clinical trials and concerns regarding safety issues of these drugs. Azithromycin (AZ) has amazing lung tissue access, wide range antibacterial efficacy, conceivable antiviral action against COVID-19. It also showed efficacy when combined with other antiviral drugs in limited clinical trials, but many clinicians raise concerns regarding cardiovascular risk in susceptible patients. DOX has a considerable role in the management of pneumonia, it has some advantages including cardiac safety, very good access to lung tissue, potential antiviral, and immunomodulation impact by several mechanisms. The pharmacological profiles of both drugs are heightening considering these medications for further studies in the management of COVID-19.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7797177PMC
http://dx.doi.org/10.1016/j.arabjc.2020.102983DOI Listing

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