Comprehensive Pharmacovigilance Analysis of Lebrikizumab: A Real-World Safety Assessment Based on the FDA Adverse Event Reporting System (FAERS) Database

Maohua Chen; Chengjie Ke; Yaping Huang

doi:10.1080/08923973.2026.2648209

March 23, 2026Immunopharmacology and Immunotoxicology

Comprehensive Pharmacovigilance Analysis of Lebrikizumab: A Real-World Safety Assessment Based on the FDA Adverse Event Reporting System (FAERS) Database

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Key Points

The aim is to assess the safety profile of lebrikizumab using real-world data from the FAERS database.
Conducted a pharmacovigilance analysis using the FDA Adverse Event Reporting System (FAERS) database.
Focused on analyzing reported adverse events associated with lebrikizumab.
Evaluated safety data to determine long-term usability in clinical settings.
Lebrikizumab demonstrates a favorable safety profile.
Adverse event reports indicate the safety of lebrikizumab is manageable.
Supports the use of lebrikizumab for long-term clinical practice.

Implication

This analysis evaluates lebrikizumab's safety in real-world settings, indicating its suitability for long-term use.

Abstract

This study provides a comprehensive overview of the safety of lebrikizumab and confirms that it has a favorable and manageable safety profile, supporting its suitability for long-term use in clinical practice.

Discussion

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Cite This Study

Chen et al. (2026) studied this question.

synapsesocial.com/papers/69c37b93b34aaaeb1a67e242 https://doi.org/10.1080/08923973.2026.2648209

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Comprehensive Pharmacovigilance Analysis of Lebrikizumab: A Real-World Safety Assessment Based on the FDA Adverse Event Reporting System (FAERS) Database

Key Points

Implication

Abstract

Discussion

Cite This Study

Comprehensive Pharmacovigilance Analysis of Lebrikizumab: A Real-World Safety Assessment Based on the FDA Adverse Event Reporting System (FAERS) Database

Key Points

Implication

Abstract

Discussion

Cite This Study

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