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

Tingxi Wua Department of Pharmacy, Beijing Tiantan Hospital, Capital Medical University, Beijing, ChinaView further author information

Yanfeng Shib Center of excellence for Omics Research, National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital, Capital Medical University, Beijing, ChinaView further author information

Chang Xuc Clinical Trials Institutions for Drugs and Medical devices, Beijing Shijitan Hospital, Capital Medical University, Beijing, ChinaView further author information

Bin Zhua Department of Pharmacy, Beijing Tiantan Hospital, Capital Medical University, Beijing, ChinaView further author information

Dandan Lid Department of Pharmacy, Beijing Friendship Hospital, Capital Medical University, Beijing, ChinaView further author information

Zhe Lid Department of Pharmacy, Beijing Friendship Hospital, Capital Medical University, Beijing, ChinaView further author information

Zhigang Zhaoa Department of Pharmacy, Beijing Tiantan Hospital, Capital Medical University, Beijing, ChinaCorrespondence[email protected]
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Yang Zhangd Department of Pharmacy, Beijing Friendship Hospital, Capital Medical University, Beijing, China;e 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, ChinaCorrespondence[email protected]
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A pharmacovigilance study of adverse events associated with polymyxins based on the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS) database

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

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