Prevalence and Predictors of Adverse Drug Events from Favipiravir in Patients with Coronavirus Disease 2019

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Duangkamon Poolpun
Theera Tungkasemsamran
Chiraphong Auttamalang
Yuttana Wongsalap

Abstract

Objective: To investigate the prevalence and predictors of adverse drug events associated with favipiravir use in the treatment of patients with Coronavirus Disease 2019 (COVID-19). Methods: This retrospective study analyzed data from electronic databases and inpatient medical records at Buddhachinaraj Hospital, Phitsanulok, between April 1, 2021 and December 31, 2021. The study included patients aged 18 and older who were hospitalized with COVID-19 and treated with favipiravir. Prevalence and predictors of adverse drug events from favipiravir were analyzed using descriptive statistics and logistic regression. Results: A total of 2,231 COVID-19 patients treated with favipiravir were included in the study. The mean age was 46.96±17.24 years. COVID-19 was diagnosed via RT-PCR in 1,920 patients (86.1%), and 399 patients (17.9%) were admitted to intensive care units. Adverse drug events from favipiravir occurred in 171 patients (7.7%), with elevated liver enzymes being the most common (104 patients, 4.7%). Other adverse events included dizziness, rash, hyperuricemia, and diarrhea. Predictors of adverse events from favipiravir included concurrent use of steroids (adjusted OR = 1.58, 95% CI = 1.10-2.26, P = 0.013) and parenteral anticoagulants (adjusted OR = 1.98, 95% CI = 1.24-3.16, P = 0.004). Conclusion: Rate of adverse drug events from favipiravir in the treatment of COVID-19 patients were 7.7%. Common adverse drug events included elevated liver enzymes, dizziness, rash, hyperuricemia, and diarrhea. The predictive factors associated with adverse events include receiving steroids and parenteral anticoagulants in concurrent with favipiravir.

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