The use and safety risk of repurposed drugs for COVID-19 patients: lessons learned utilizing the Food and Drug Administration’s Adverse Event Reporting System

Objectives: This study was designed to assess the disproportionality analyses of adverse drug reactions (ADRs) related to hydroxychloroquine and remdesivir and how ADR reporting fluctuated during the COVID-19 pandemic. Methods: A retrospective observational study was conducted utilizing the Food and...

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Bibliographic Details
Published in:Saudi Pharmaceutical Journal
Main Authors: Deemah S. Alsuhaibani, Heba H. Edrees, Thamir M Alshammari
Format: Article
Language:English
Published: Springer 2023-07-01
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1319016423001494