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Post-marketing safety surveillance of dalfampridine for multiple sclerosis using FDA adverse event reporting system

Objective: To investigate and analyze the post-marketing adverse event (AE) data of multiple sclerosis (MS) therapeutic drug dalfampridine using the US Food and Drug Administration Adverse Event Reporting System (FAERS) for its clinical safety application.Methods: Use OpenVigil2.1 platform to obtain...

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Bibliographic Details
Main Authors:	Rui Xiong (Author), Jing Lei (Author), Sicen Pan (Author), Hong Zhang (Author), Yongtao Tong (Author), Wei Wu (Author), Yi Huang (Author), Xiaodan Lai (Author)
Format:	Book
Published:	Frontiers Media S.A., 2023-09-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
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