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Authors
Gupte, Vaishali http://orcid.org/0000-0003-4439-2416
Hegde, Rashmi
Sawant, Sandesh
Kalathingal, Kabil
Jadhav, Sonali
Malabade, Rohit
Gogtay, Jaideep
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Funding
Funding for this research was provided by:
Cipla Ltd., India
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Article History
Received: 23 March 2021
Accepted: 22 December 2021
First Online: 4 January 2022
Declarations
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: There was no need for administrative permissions, since it was mandatory for all hospitals and clinics that administered remdesivir in COVID-19 patients to provide data (through an active surveillance form) thus, obtaining ethical approval and informed consent was not required. As a part of regulatory approval, Cipla Ltd has to provide the data report to Central Drugs Standard Control Organisation (CDSCO) periodically. The data were anonymised before its use.
: Not applicable.
: All the authors are permanent employees of Cipla Ltd., India who had a role in the study. The study was funded by Cipla Ltd., India, and was the provider of the drug.
