Drug-induced dementia: a real-world pharmacovigilance study using the FDA Adverse Event Reporting System database
Background: 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 safet...
| Published in: | Therapeutic Advances in Neurological Disorders |
|---|---|
| Main Authors: | , , , , |
| Format: | Article |
| Language: | English |
| Published: |
SAGE Publishing
2025-01-01
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| Online Access: | https://doi.org/10.1177/17562864251315137 |