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10.1016/j.amjms.2020.05.044

http://scihub22266oqcxt.onion/10.1016/j.amjms.2020.05.044
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32622469!7833957!32622469
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suck abstract from ncbi


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pmid32622469      Am+J+Med+Sci 2020 ; 360 (3): 216-221
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  • Is Inhaled Furosemide a Potential Therapeutic for COVID-19? #MMPMID32622469
  • Brennecke A; Villar L; Wang Z; Doyle LM; Meek A; Reed M; Barden C; Weaver DF
  • Am J Med Sci 2020[Sep]; 360 (3): 216-221 PMID32622469show ga
  • The potentially lethal infection caused by the novel Severe Acute Respiratory Disease Coronavirus-2 (SARS-CoV-2) has evolved into a global crisis. Following the initial viral infection is the host inflammatory response that frequently results in excessive secretion of inflammatory cytokines (e.g., IL-6 and TNFalpha), developing into a self-targeting, toxic "cytokine storm" causing critical pulmonary tissue damage. The need for a therapeutic that is available immediately is growing daily but the de novo development of a vaccine may take years. Therefore, repurposing of approved drugs offers a promising approach to address this urgent need. Inhaled furosemide, a small molecule capable of inhibiting IL-6 and TNFalpha, may be an agent capable of treating the Coronavirus Disease 2019 cytokine storm in both resource-rich and developing countries. Furosemide is a "repurpose-able" small molecule therapeutics, that is safe, easily synthesized, handled, and stored, and is available in reasonable quantities worldwide.
  • |Administration, Inhalation[MESH]
  • |Antiviral Agents/administration & dosage/pharmacokinetics[MESH]
  • |Betacoronavirus/*drug effects/immunology/metabolism[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/*drug therapy/immunology/metabolism[MESH]
  • |Furosemide/*administration & dosage/pharmacokinetics[MESH]
  • |Humans[MESH]
  • |Immunity, Innate/*drug effects/physiology[MESH]
  • |Inflammation Mediators/antagonists & inhibitors/immunology/metabolism[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/*drug therapy/immunology/metabolism[MESH]
  • |SARS-CoV-2[MESH]


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