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論文・技術情報

• • An Exploratory Research to Evaluate the 30 Most Common Pulmonary Embolism Drugs in the Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/6/6
  • A real-world disproportionality analysis of Tenofovir Alafenamide (TAF): Data mining of the FDA adverse event reporting system (FAERS).
    タグ:

    • FAERS
    2025/6/5
  • An Evaluation of Duplicate Adverse Event Reports Characteristics in the Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/6/5
  • Immune-mediated enterocolitis is associated with immune checkpoint inhibitors: A pharmacovigilance study from the FDA Adverse Event Reporting System (FAERS) database.
    タグ:

    • FAERS
    2025/6/4
  • A disproportionality analysis of nervous system adverse events associated with disease-modifying therapies in multiple sclerosis: insights from the FDA adverse event reporting system (FAERS).
    タグ:

    • FAERS
    2025/6/4
  • Comparative disproportionality analysis of adverse events associated with combined therapy versus monotherapy of abiraterone and olaparib for prostate cancer: a pharmacovigilance study using the FAERS database.
    タグ:

    • FAERS
    2025/6/4
  • Post-marketing safety surveillance of voclosporin: an observational, pharmacovigilance study leveraging faers database study on the safety of voclosporin.
    タグ:

    • FAERS
    2025/6/3
  • Risk Assessment of Linezolid-Associated Neurological Adverse Drug Reactions Based on the Food and Drug Administration Adverse Event Reporting System Database.
    タグ:

    • FAERS
    2025/6/3
  • Adverse cardiac events associated with antibody-drug conjugates in cancer patients: retrospective analysis of FAERS database and RCTs.
    タグ:

    • FAERS
    2025/6/2
  • Adverse events associated with vismodegib: insights from a real-world pharmacovigilance study using the FAERS database.
    タグ:

    • FAERS
    2025/6/2

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