Pulmonary adverse events associated with monoclonal antibodies approved for multiple myeloma: a pharmacovigilance study based on the FDA adverse event reporting system

This study summarized significant pulmonary adverse event signals associated with monoclonal antibodies approved for myeloma, emphasizing the significance of monitoring interstitial lung disease, respiratory failure, and infective pneumonia.

Authors

Ting Liang (ORCID: https://orcid.org/0000-0002-7924-5195)
Cong Xu (ORCID: https://orcid.org/0000-0003-3310-815X)
Dongzheng Gai
Junfeng Li (ORCID: https://orcid.org/0000-0001-9876-695X)
Limei Yan

Institutions

Sun Yat-sen University (CN)
Changzhi Medical College (CN)

Publication Details

Journal: Expert Opinion on Drug Safety
Published: 2025-04-30
DOI: https://doi.org/10.1080/14740338.2025.2499218
Primary Topic: Pharmacovigilance and Adverse Drug Reactions
Type: article
Field-Weighted Citation Impact: 0.00

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article

Pulmonary adverse events associated with monoclonal antibodies approved for multiple myeloma: a pharmacovigilance study based on the FDA adverse event reporting system

Ting Liang, Cong Xu, Dongzheng Gai, Junfeng Li et al.

Apr 30, 2025

6 links

Expert Opinion on Drug Safety

Pharmacovigilance and Adverse Drug Reactions

article

Pulmonary adverse events associated with monoclonal antibodies approved for multiple myeloma: a pharmacovigilance study based on the FDA adverse event reporting system

Ting Liang, Cong Xu, Dongzheng Gai, Junfeng Li, Limei Yan

April 30, 2025article en

Abstract

Expert Opinion on Drug Safety

Sun Yat-sen University (CN), Changzhi Medical College (CN)

Good health and well-being

Openalex Percentile: Top 91%

Pharmacovigilance and Adverse Drug Reactions

DOI Source OpenAlex

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Pulmonary adverse events associated with monoclonal antibodies approved for multiple myeloma: a pharmacovigilance study based on the FDA adverse event reporting system — Ting Liang, Cong Xu, et al. · Expert Opinion on Drug Safety (2025) | TGRS Research Map | TGRS