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Adverse events associated with IL-23 and IL-12/23 inhibitors in the clinical management of psoriasis: a comprehensive pharmacovigilance analysis.
タグ:
FAERS
2025/1/21
A multidimensional assessment of adverse events associated with paliperidone palmitate: a real-world pharmacovigilance study using the FAERS and JADER databases.
タグ:
JADER
FAERS
2025/1/21
A Real-World Data Analysis of Alglucosidase Alfa in the FDA Adverse Event Reporting System (FAERS) Database.
タグ:
FAERS
2025/1/21
Analysis of Drug-Related Tinnitus Based on the FDA Adverse Event Reporting System Database.
タグ:
FAERS
2025/1/20
Drug-induced Parkinson-like events: a real-world study from 2004 to the first quarter of 2024 based on FAERS.
タグ:
FAERS
2025/1/20
Evaluation of the safety profile of amivantamab based on real-world evidence: a call to vigilance.
タグ:
FAERS
2025/1/20
A disproportionality analysis of FDA adverse event reporting system events for misoprostol.
タグ:
FAERS
2025/1/20
Adverse Events of Factor Xa Inhibitors in Pediatric Patients: A Meta-analysis and Pharmacovigilance Study.
タグ:
FAERS
2025/1/18
A pharmacovigilance study on the safety of faricimab in real-world scenario using FDA adverse event reporting system database.
タグ:
FAERS
2025/1/18
A real-world Pharmacovigilance study of brodalumab based on the FDA adverse event reporting system.
タグ:
FAERS
2025/1/18
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