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Response to FDA Adverse Event Reporting System (FAERS) Essentials: A Reflection on Study Conception.
タグ:
FAERS
2025/8/20
FDA Adverse Event Reporting System Essentials: A Reflection on Study Conception.
タグ:
FAERS
2025/8/20
Ductus Arteriosus Variability Linked to Maternal Drug Exposure: Assessment of the USFDA Adverse Event Reporting System using Disproportionality Analysis.
タグ:
FAERS
2025/8/15
A disproportionality analysis of FDA adverse event reporting system (FAERS) events for methimazole and propylthiouracil.
タグ:
FAERS
2025/8/14
Post-marketing safety concerns with dolutegravir: a pharmacovigilance study based on the FDA adverse event reporting system database.
タグ:
FAERS
2025/8/14
Identification of potential drug-induced neuralgia signals through disproportionality analysis of the FAERS database.
タグ:
FAERS
2025/8/14
Exploring Adverse Event Associations of Predicted PXR Agonists Using the FAERS Database.
タグ:
FAERS
2025/8/14
Pharmacovigilance of five commonly used antibiotics in acute exacerbations of COPD (AECOPD): Analysis of the FDA adverse event reporting system database.
タグ:
FAERS
2025/8/14
Safety of antidepressants commonly used in 6-17-year-old children and adolescents: A disproportionality analysis from 2014-2023 on the basis of the FAERS database.
タグ:
FAERS
2025/8/13
Signal mining for non-bleeding adverse event in novel oral anticoagulants: a pharmacovigilance study based on FAERS database.
タグ:
FAERS
2025/8/13
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