Remdesivir for COVID-19 pneumonia in patients with severe chronic kidney disease: A Case series and review of the literature
Remdesivir was the first antiviral agent to receive FDA authorization for severe COVID-19 management, which restricts its use with severe renal impairment due to concerns that active metabolites might accumulate, causing renal toxicities. With limited treatment options, available evidence on such pa...
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Published in | Clinical Case Reports Vol. 10; no. 2 |
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Main Authors | , , , , , , , |
Format | Report |
Language | English |
Published |
Hoboken
John Wiley & Sons, Inc
01.02.2022
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Online Access | Get full text |
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Summary: | Remdesivir was the first antiviral agent to receive FDA authorization for severe COVID-19 management, which restricts its use with severe renal impairment due to concerns that active metabolites might accumulate, causing renal toxicities. With limited treatment options, available evidence on such patient groups is important to assess for future safety. |
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DOI: | 10.1002/ccr3.5467 |