Monitoring Adverse Drug Events in Web Forums: Evaluation of a Pipeline and Use Case Study
BackgroundTo mitigate safety concerns, regulatory agencies must make informed decisions regarding drug usage and adverse drug events (ADEs). The primary pharmacovigilance data stem from spontaneous reports by health care professionals. However, underreporting poses a notable challenge within the cur...
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| フォーマット: | 図書 |
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JMIR Publications,
2024-06-01T00:00:00Z.
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| 請求記号: |
A1234.567 |
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| 所蔵 1 | 利用可 |