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Post marketing safety assessment of the novel postpartum depression drug, Zuranolone: evidence from real-world pharmacovigilance analysis based on the FDA adverse event reporting system.
タグ:
FAERS
2025/9/2
Seasonality and Trends in Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis Before and During the COVID-19 Pandemic: A Pharmacovigilance Study.
タグ:
FAERS
2025/9/2
Aioli: Standardising Drugs in the FDA Adverse Event Reporting System (FAERS) to RxNorm and Anatomical Therapeutic Chemical (ATC) Codes.
タグ:
FAERS
2025/9/5
Pharmacovigilance study of ramucirumab: A safety analysis based on the FDA adverse event reporting system.
タグ:
FAERS
2025/9/4
Characterizing the Real-World Risks of Kidney Injuries Associated with Chimeric Antigen Receptor T Cell Therapies-Evidence and Safety.
タグ:
FAERS
2025/9/4
Association of Anti-VEGF Therapy with Reported Ocular Adverse Events: A Global Pharmacovigilance Analysis.
タグ:
FAERS
2025/9/4
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
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