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論文・技術情報

• • Safety concerns of aztreonam: a real-world disproportionality analysis based on FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2024/11/20
  • Aplastic anemia associated with osimertinib: Analysis of the FDA adverse event reporting system.
    タグ:

    • FAERS
    2024/11/20
  • Pharmacovigilance study of famciclovir in the Food and Drug administration adverse event reporting system database.
    タグ:

    • FAERS
    2024/11/20
  • Comparative Post-Marketing Surveillance of Memantine and Cholinesterase Inhibitors: Cardiovascular Adverse Events With a Focus on Sex Differences Using the FDA Adverse Event Reporting System Database.
    タグ:

    • FAERS
    2024/11/20
  • Updated insights into adverse events associated with mepolizumab: a disproportionality analysis from the FDA adverse event reporting system database.
    タグ:

    • FAERS
    2024/11/22
  • Comprehensive Analysis of Mitotane-Related Adverse Events Using the Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2024/11/22
  • Adverse event reporting of combining SGLT2 inhibitor and GLP1 receptor agonist: A real-world study from FAERS.
    タグ:

    • FAERS
    2024/11/22
  • KRAS-G12 inhibitors in lung cancer therapy: unveiling the toxicity profile through a pharmacovigilance study.
    タグ:

    • FAERS
    2024/11/21
  • Analysis of tirzepatide in the US FDA adverse event reporting system (FAERS): a focus on overall patient population and sex-specific subgroups.
    タグ:

    • FAERS
    2024/11/21
  • Comparison of safety profiles for dapagliflozin based on EMA and FDA safety issues: Challenges and future of post-marketing surveillance in Korea.
    タグ:

    • KAERS
    • FAERS
    2024/11/22

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