Diverse Scientific Research StudiesCOVID-19 Prevention and ImpactCOVID-19 Clinical Research Studies

A. Rusli, A. R. Hasugian, Harli Amir Mahmudji, S. Rahardjo, Hadjar Siswantoro, Rossa Avrina, A. K. Syarif, Nurhayati Nurhayati, M. Susilawati, V. Setiawaty

2026.2.15Bulletin of Pharmaceutical Sciences. Assiut

DOI: 10.21608/bfsa.2026.403216.2637

Abstract

Aims: It is anticipated that adding favipiravir, one of the promising antivirals, to Azithromycin will be able to eradicate SARS-CoV-2. The purpose of this study was to evaluate the safety and effectiveness of using Azithromycin and favipiravir together to treat patients with confirmed moderate COVID-19. Methods: Patients with moderate symptoms who were proven to be positive for COVID-19 were included in the experimental, intervention, randomized, open-label trial. Results: Out of the 200 subjects that were originally planned, 130 were recruited. Based on "symptom-free and negative PCR" on day 7 by Intention To Treat (ITT), the efficacy of Azithromycin with favipiravir was found to be 10.61% vs 3.12%, although not significantly different (P=0.3608) from Azithromycin alone. The most frequent side effects of both medications, which are safe and well-tolerated, are headache and diarrhea. Conclusion: The study's conclusion was that Azithromycin + favipiravir was equally as effective as Azithromycin by itself. Despite their poor efficacy, both therapy methods are well-tolerated and safe.

Citation format

RUSLI, A., et al. Treatment moderate covid-19 by favipiravir and azithromycin in indonesia: Lesson learnt for safety and effectiveness. Bulletin of Pharmaceutical Sciences Assiut, 2026, 0(0): 0.