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• • Venous Thromboembolism with Combined Oral Contraceptives Based on Estrogen and Progestin Content: A disproportionality analysis of the United States Food and Drug Administration Adverse Event Reporting System database.
    タグ:

    • FAERS

    2026/3/7
  • Long-term safety evaluation of mirtazapine: A real-world pharmacovigilance study based on the FAERS database.
    タグ:

    • FAERS

    2026/3/6
  • Unveiling the risk: A comprehensive analysis of drug-induced aphthous ulcers using real-world data from FAERS.
    タグ:

    • FAERS

    2026/3/6
  • Data mining and analysis of adverse drug events of propofol in the general population and the elderly based on the US Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS

    2026/3/6
  • Fluoroquinolones and the risk of panic attacks: a systematic review and disproportionality analysis using individual case safety reports from the FDA Adverse Event Reporting System (FAERS) database.
    タグ:

    • CVAR
    • FAERS

    2026/3/6
  • Cutaneous adverse events associated with Rybrevant based on FDA adverse event reporting system (FAERS) database from 2021 to 2024.
    タグ:

    • FAERS

    2026/3/6
  • Comparative safety profiles of risankizumab versus guselkumab: a pharmacovigilance study based on the FAERS database.
    タグ:

    • FAERS

    2026/3/6
  • Appendicitis and multiple sclerosis disease-modifying therapies: a disproportionality analysis of the FDA adverse event reporting system.
    タグ:

    • FAERS

    2026/3/6
  • Assessing safety trends of withdrawn medications: A data-driven pharmacovigilance approach using growth models.
    タグ:

    • FAERS

    2026/3/5
  • Descriptive analysis of anaphylactic events reported in the FDA Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS

    2026/3/5

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