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Evaluating the efficacy, safety, and immunogenicity of FDA-approved RSV vaccines: a systematic review of Arexvy, Abrysvo, and mResvia.
タグ:
VAERS
FAERS
2025/9/3
Stacking the Risks: Fatal Consequences of Anabolic Steroid Misuse and Stacked Substance Use in FAERS Data.
タグ:
KAERS
FAERS
2025/9/5
Safety assessment of laronidase: real-world adverse event analysis based on the FDA adverse event reporting system (FAERS).
タグ:
FAERS
2025/9/5
Drug-induced gingival diseases: insights from the FDA Adverse Event Reporting System (FAERS) database analysis.
タグ:
FAERS
2025/8/30
Unveiling the hidden risk of caspofungin: insights from three adverse event reporting systems and network pharmacology integration.
タグ:
JADER
FAERS
2025/8/31
A real-world pharmacovigilance study of FDA Adverse Event Reporting System (FAERS) events for Definity.
タグ:
FAERS
2025/9/1
Contemporary local anaesthetic-associated adverse events and mortality: a pharmacovigilance analysis of a US reporting system.
タグ:
FAERS
2025/8/29
Ocular safety evaluation of toplic and systemic antifungal medications: A multi-source pharmacovigilance and genomic study.
タグ:
FAERS
2025/8/29
A disproportionality analysis of adverse events caused by pexidartinib from the FDA adverse event reporting system.
タグ:
FAERS
2025/8/30
Real-world safety profile of mitomycin: signal detection and time-to-onset analysis from FDA adverse event reporting system and VigiAccess databases.
タグ:
FAERS
2025/8/28
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