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論文・技術情報

• • Isotretinoin-related adverse sexual and reproductive outcomes: a real-world pharmacovigilance study of the FDA Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2025/12/25
  • Toxicity profiles of cyclin-dependent kinase 4/6 inhibitors: safety analysis from clinical trials and the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/12/29
  • A real-world disproportionality analysis of roflumilast using the US food and drug administration adverse event reporting system data.
    タグ:

    • FAERS
    2025/12/29
  • Vismodegib and Sonidegib Are Associated With an Elevated Reporting Odds of Squamous Cell Carcinoma; a Comparative Pharmacovigilance Study of the FDA Adverse Events Reporting System (FAERS).
    タグ:

    • FAERS
    2025/12/27
  • A real-world pharmacovigilance study of modafinil events in the FDA Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2025/12/27
  • Melanosis Secondary to Drugs: A Real-World Pharmacovigilance Study of the FDA Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2025/12/26
  • The guanylate cyclase stimulator vericiguat: Insights and adverse events from a FAERS-based pharmacovigilance study.
    タグ:

    • FAERS
    2025/12/30
  • Adverse events following measles, mumps, rubella and varicella virus vaccine live (PROQUAD((R))) reported to the vaccine adverse event reporting system (VAERS), 2015-2025.
    タグ:

    • VAERS
    • FAERS
    2025/12/30
  • A 20-year FAERS analysis of hypersensitivity reports to chlorhexidine and povidone-iodine (2004-2024).
    タグ:

    • FAERS
    2025/12/29
  • Disproportionality analysis of safety signals for milnacipran and levomilnacipran: a pharmacovigilance study using the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/12/29

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