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Original Article
13 (
1
); 74-79

A STUDY OF FAVIPIRAVIR IN HOSPITALIZED COVID-19 PATIENTS, EXPERIENCE FROM A SINGLETERTIARY CARE CENTRE

Assistant Professor, Department of General Medicine, Smt. NHL Municipal Medical College and SVP IMSR Hospital, Ahmedabad
Professor, Department of General Medicine, Smt. NHL Municipal Medical College and SVP IMSR Hospital, Ahmedabad
Ex Resident Doctor, Department of General Medicine, Smt. NHL Municipal Medical College and SVP IMSR Hospital, Ahmedabad
Third Year Resident Doctor, Department of General Medicine, Smt. NHL Municipal Medical College and SVP IMSR Hospital, Ahmedabad
Second Year Resident Doctor, Department of General Medicine, Smt. NHL Municipal Medical College and SVP IMSR Hospital, Ahmedabad

*Corresponding Author: Dr. Sneha S. Shah, E-mail: drsneha906@gmail.com

Licence
This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

Abstract

Background:

Various therapeutic modalities are under evaluation for the COVID-19 pandemic which has gripped the world, India being badly affected. Favipiravir is one of the newer antivirals approved by DCGI for use in COVID-19 pneumonia in June 2020. Our study aims to evaluate its efficacy and safety profile.

Methods:

Ours is a retrospective observational study involving patients given favipiravir as per protocol in June. A historical cohort of patients admitted in April through May was used for comparison.

Results:

A total of 69 patients were studied in the favipiravir arm as compared to 400 in the Standard of Care group. 65 (94.20%) patients given favipiravir tested negative by the 10th day whereas in the SOC group, 224 (56%)patients out of 400 tested negative. 17 (24.64%) patients given favipiravir were on oxygen support which reduced to 0 (0%) on day 10, where as in the SOC group, 49 (12.25%) patients were on oxygen support initially which increased to 54 (13.5%). 12 (17.39%) patients administered favipiravir developed mild transaminits and 3 (4.35%) patients developed diarrhoea.

Conclusion:

Favipiravir is effective in mild to moderate COVID-19 pneumonia for enhancing viral clearance and resulted in clinical improvement.

Keywords

Adverse Effects
Antivirals
Clinical Improvement
COVID-19
Favipiravir
Viral Clearance

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