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Postmarketing safety evaluation of belimumab: a pharmacovigilance analysis

Objective The present study aimed to provide a comprehensive evaluation of the postmarketing safety of belimumab based on the Food and Drug Administration Adverse Event Reporting System (FAERS) database.Methods Adverse event (AE) reports in the FAERS database from January 2021 to December 2023 were...

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Principais autores: Huqun Li, Wenlong Xie, Chongshu Wang, Cuilian Guo
Formato: Artigo
Idioma:Inglês
Publicado: BMJ Publishing Group 2025-01-01
Series:Lupus Science and Medicine
Acceso en liña:https://lupus.bmj.com/content/12/1/e001400.full
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