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Post-marketing safety of immunomodulatory drugs in multiple myeloma: A pharmacovigilance investigation based on the FDA adverse event reporting system
Objective: In recent years, the emergence of immunomodulatory drugs (IMiDs) has significantly improved clinical outcomes in patients with multiple myeloma (MM); however, serious adverse events (AEs) have hindered their safe clinical application. This study aimed to characterize the safety profiles a...
Autores principales: | Jiang, Tingting, Su, Hui, Li, Yanping, Wu, Yuanlin, Ming, Yue, Li, Chen, Fu, Ruoqiu, Feng, Lu, Li, Ziwei, Li, Li, Ni, Rui, Liu, Yao |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751748/ https://www.ncbi.nlm.nih.gov/pubmed/36532784 http://dx.doi.org/10.3389/fphar.2022.989032 |
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