Analysis of tirzepatide in the US FDA adverse event reporting system (FAERS): a focus on overall patient population and sex-specific subgroups

This study provides valuable insights into the occurrence of ADEs following tirzepatide administration, potentially supporting clinical monitoring and risk identification efforts.

Authors

Institutions

Publication Details

Journal
Frontiers in Pharmacology
Published
2024-11-06
DOI
https://doi.org/10.3389/fphar.2024.1463657
Citations
16
Primary Topic
Pharmacovigilance and Adverse Drug Reactions
Type
article
Field-Weighted Citation Impact
5.61

Funders

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article

Analysis of tirzepatide in the US FDA adverse event reporting system (FAERS): a focus on overall patient population and sex-specific subgroups

Zhiwei Cui, Ruizhen Zhao, Junyou Chen, Fan Zou et al.
16 citations
Frontiers in Pharmacology
Pharmacovigilance and Adverse Drug Reactions
5.61
article

Analysis of tirzepatide in the US FDA adverse event reporting system (FAERS): a focus on overall patient population and sex-specific subgroups

Zhiwei Cui, Ruizhen Zhao, Junyou Chen, Fan Zou, Li Wang, Liyuan Zhou, Siyu Lou, Yingyong Ou, Chengyu Zhu
article en
16 citations

Abstract

This study provides valuable insights into the occurrence of ADEs following tirzepatide administration, potentially supporting clinical monitoring and risk identification efforts.

Frontiers in PharmacologyVol. 15
Zunyi Medical University (CN), First Affiliated Hospital of Xi'an Jiaotong University (CN)
Health Commission of Guizhou Province
Good health and well-being
Openalex Percentile: Top 3%
Pharmacovigilance and Adverse Drug Reactions
5.61
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