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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
Second-generation antipsychotic-induced dystonia: Analysis using the Japanese Adverse Drug Event Report (JADER) database.
タグ:
JADER
2025/1/21
Analyses of Adverse Drug Reactions to Fluoroquinolones in Spontaneous Reports Before and After the Referral and in Clinical Routine Cases.
タグ:
EudraVigilance
2025/1/21
From bench to bedside: elucidating VEGF(R) inhibitor-related heart failure in cancer treatment.
タグ:
VigiBase
2025/1/24
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