Post-marketing safety of elacestrant in breast cancer: a pharmacovigilance investigation using the FDA adverse event reporting system

FAERS data analyses were conducted to evaluate the safety of post-marketing clinical use of elacestrant and to ensure that physicians identify the risk factors for the AEs of this drug.

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Publication Details

Journal
BMC Pharmacology and Toxicology
Published
2025-03-11
DOI
https://doi.org/10.1186/s40360-025-00887-2
Citations
1
Primary Topic
Biomedical Ethics and Regulation
Type
article
Field-Weighted Citation Impact
1.16
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article

Post-marketing safety of elacestrant in breast cancer: a pharmacovigilance investigation using the FDA adverse event reporting system

Ziyi Fan, Shuang Guo, Bin Song, Yanan Xu
1 citations
BMC Pharmacology and Toxicology
Biomedical Ethics and Regulation
1.16
article

Post-marketing safety of elacestrant in breast cancer: a pharmacovigilance investigation using the FDA adverse event reporting system

Ziyi Fan, Shuang Guo, Bin Song, Yanan Xu
article en
1 citations

Abstract

FAERS data analyses were conducted to evaluate the safety of post-marketing clinical use of elacestrant and to ensure that physicians identify the risk factors for the AEs of this drug.

BMC Pharmacology and ToxicologyVol. 26(1)
Shanxi Medical University (CN), Second Hospital of Shanxi Medical University (CN), Shanxi Academy of Medical Sciences (CN)
Good health and well-being
Openalex Percentile: Top 25%
Biomedical Ethics and Regulation
1.16
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