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論文・技術情報

• • Adverse event profiles of drug-induced decreased libido: an assessment of the US food and drug administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2024/9/30
  • Real-World Large Sample Assessment of Drug-related Dry Eye Risk: Based on the FDA Adverse Event Reporting System Database.
    タグ:

    • FAERS
    2024/9/30
  • Safety assessment of KRAS (G12C) inhibitors based on the FDA Adverse Event Reporting System (FAERS) database: A real-world pharmacovigilance study.
    タグ:

    • FAERS
    2024/9/30
  • Herpes virus reactivation induced by abrocitinib: A real-world pharmacovigilance analysis of the FDA Adverse Event Reporting System (FAERS) database.
    タグ:

    • FAERS
    2024/9/29
  • A real-world pharmacovigilance study using disproportionality analysis of United States Food and Drug Administration Adverse Event Reporting System events for vinca alkaloids: comparing vinorelbine and Vincristine.
    タグ:

    • FAERS
    2024/9/28
  • Adverse events associated with azithromycin and clarithromycin in adults aged >/=65: a disproportionality analysis of the FDA Adverse Event Reporting System (FAERS) database.
    タグ:

    • FAERS
    2024/10/2
  • Rhabdomyolysis associated with concomitant use of colchicine and statins in the real world: identifying the likelihood of drug-drug interactions through the FDA adverse event reporting system.
    タグ:

    • FAERS
    2024/10/1
  • Pancreatitis Associated With Teduglutide: A Disproportionality Analysis via the Food and Drug Administration Adverse Event Reporting System (FAERS) Database.
    タグ:

    • FAERS
    2024/10/1
  • Neratinib safety evaluation: real-world adverse event analysis from the FAERS database.
    タグ:

    • FAERS
    2024/9/30
  • Adverse events associated with SARS-CoV-2 neutralizing monoclonal antibodies using the FDA adverse event reporting system database.
    タグ:

    • KAERS
    • VAERS
    • FAERS
    2024/9/30

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