A pharmacovigilance study of adverse events associated with polymyxins based on the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS) database-Reference-Cited by-同舟云学术

A pharmacovigilance study of adverse events associated with polymyxins based on the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS) database

Published:2024-05 Issue: Volume: Page:1-9
ISSN:1474-0338
Container-title:Expert Opinion on Drug Safety
language:en
Short-container-title:Expert Opinion on Drug Safety

Author:

Wu Tingxi¹,Shi Yanfeng²,Xu Chang³,Zhu Bin¹,Li Dandan⁴,Li Zhe⁴,Zhao Zhigang¹,Zhang Yang⁴⁵

Affiliation:

1. Department of Pharmacy, Beijing Tiantan Hospital, Capital Medical University, Beijing, China

2. Center of excellence for Omics Research, National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital, Capital Medical University, Beijing, China

3. Clinical Trials Institutions for Drugs and Medical devices, Beijing Shijitan Hospital, Capital Medical University, Beijing, China

4. Department of Pharmacy, Beijing Friendship Hospital, Capital Medical University, Beijing, China

5. Beijing Key Laboratory of Molecular Pharmaceutics and New Drug Delivery Systems, State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, China

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/14740338.2024.2348610

Reference41 articles.

1. Rescuing the Last-Line Polymyxins: Achievements and Challenges

2. Colistin: The Revival of Polymyxins for the Management of Multidrug-Resistant Gram-Negative Bacterial Infections

3. Polymyxin-induced nephrotoxicity and its predictors: a systematic review and meta-analysis of studies conducted using RIFLE criteria of acute kidney injury

4. Evaluation of prognosis and nephrotoxicity in patients treated with colistin in intensive care unit

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