Drug-induced dementia: a real-world pharmacovigilance study using the FDA Adverse Event Reporting System database
Dementia is a serious adverse event (AE) that requires attention in clinical practice. However, information on drug-induced dementia is limited. The U.S. FDA Adverse Event Reporting System (FAERS) serves as an important resource for identifying real-world adverse drug reactions and safety signals. T...
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Published in | Therapeutic advances in neurological disorders Vol. 18; p. 17562864251315137 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
England
SAGE Publications
01.01.2025
SAGE Publishing |
Subjects | |
Online Access | Get full text |
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