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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| Main Authors: | , , , , , , , |
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| Format: | Book |
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Frontiers Media S.A.,
2023-09-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |