Cargando…
Ovary and uterus related adverse events associated with statin use: an analysis of the FDA Adverse Event Reporting System
Experimental studies have demonstrated statin-induced toxicity for ovary and uterus. However, the safety of statins on the functions of ovary and uterus in real-world clinical settings remains unknown. The aim of this study was to identify ovary and uterus related adverse events (AEs) associated wit...
Autores principales: | Jiao, Xue-feng, Li, Hai-long, Jiao, Xue-yan, Guo, Yuan-chao, Zhang, Chuan, Yang, Chun-song, Zeng, Li-nan, Bo, Zhen-yan, Chen, Zhe, Song, Hai-bo, Zhang, Ling-li |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7371681/ https://www.ncbi.nlm.nih.gov/pubmed/32686733 http://dx.doi.org/10.1038/s41598-020-68906-2 |
Ejemplares similares
-
Hyperuricaemia, gout and related adverse events associated with antihypertensive drugs: A real-world analysis using the FDA adverse event reporting system
por: Jiao, Xue-Feng, et al.
Publicado: (2023) -
Statin-Associated Muscular and Renal Adverse Events: Data Mining of the Public Version of the FDA Adverse Event Reporting System
por: Sakaeda, Toshiyuki, et al.
Publicado: (2011) -
A disproportionality analysis of adverse events associated to pertuzumab in the FDA Adverse Event Reporting System (FAERS)
por: Zou, Shu-peng, et al.
Publicado: (2023) -
Cardiac adverse events associated with quetiapine: Disproportionality analysis of FDA adverse event reporting system
por: Shu, Yamin, et al.
Publicado: (2023) -
Assessing taxane-associated adverse events using the FDA adverse event reporting system database
por: Lao, Dong-Hui, et al.
Publicado: (2021)