Profiles and influencing factors of pulmonary fibrosis associated with biologic and conventional disease-modifying antirheumatic drugs for autoimmune diseases: a disproportionality study based on FAERS and VigiAccess

This study revealed varying degrees of pulmonary fibrosis signals related to DMARDs, with significantly overreporting observed in certain conventional and biologic DMARDs. Age was identified as a key susceptibility factor. As the use of these agents expands, clinicians should remain vigilant in monitoring for pulmonary fibrosis.

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Publication Details

Journal
Frontiers in Pharmacology
Published
2025-09-25
DOI
https://doi.org/10.3389/fphar.2025.1604895
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
0.00

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article

Profiles and influencing factors of pulmonary fibrosis associated with biologic and conventional disease-modifying antirheumatic drugs for autoimmune diseases: a disproportionality study based on FAERS and VigiAccess

Jiayi He, Cheng Luo, Qian Chen, Nan Jia et al.
Frontiers in Pharmacology
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
article

Profiles and influencing factors of pulmonary fibrosis associated with biologic and conventional disease-modifying antirheumatic drugs for autoimmune diseases: a disproportionality study based on FAERS and VigiAccess

Jiayi He, Cheng Luo, Qian Chen, Nan Jia, Xinhui Wu, C. Y. Yang, Fei Wang, Xinyue Zhang
article en

Abstract

This study revealed varying degrees of pulmonary fibrosis signals related to DMARDs, with significantly overreporting observed in certain conventional and biologic DMARDs. Age was identified as a key susceptibility factor. As the use of these agents expands, clinicians should remain vigilant in monitoring for pulmonary fibrosis.

Frontiers in PharmacologyVol. 16
Chengdu University of Traditional Chinese Medicine (CN)
World Health Organization, National Natural Science Foundation of China
Openalex Percentile: Top 62%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
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