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論文・技術情報

• • PARP inhibitor-related acute renal failure: a real-world study based on the FDA adverse event reporting system database.
    タグ:

    • FAERS
    2024/7/5
  • Compartment syndrome associations with drugs: a pharmacovigilance study of the FDA adverse event reporting system (FAERS).
    タグ:

    • FAERS
    2024/7/5
  • Exploring the Relationship Between Atorvastatin and Memory Loss: A Comprehensive Analysis Integrating Real-World Pharmacovigilance and Mendelian Randomization.
    タグ:

    • FAERS
    2024/7/4
  • Analysis of hemorrhagic drug-drug interactions between P-gp inhibitors and direct oral anticoagulants from the FDA adverse event reporting system.
    タグ:

    • FAERS
    2024/7/4
  • Hepatic injury and hepatic failure adverse events in 3,4-methylenedioxymethamphetamine users reported to the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2024/7/3
  • Risk of stress cardiomyopathy associated with selective serotonin reuptake inhibitors and serotonin and norepinephrine reuptake inhibitors: a real-world pharmacovigilance analysis.
    タグ:

    • FAERS
    2024/7/3
  • Association of thrombocytopenia with immune checkpoint inhibitors: a large-scale pharmacovigilance analysis based on the data from FDA adverse event reporting system database.
    タグ:

    • FAERS
    2024/7/2
  • Sodium-glucose cotransporter-2 inhibitors and abnormal serum potassium: a real-world, pharmacovigilance study.
    タグ:

    • FAERS
    2024/7/1
  • Comparison of Infection Risks Between Various Inhaled and Intranasal Corticosteroids: A Pharmacovigilance Analysis Based on the FAERS Database.
    タグ:

    • FAERS
    2024/7/1
  • Hepatitis-related adverse events associated with immune checkpoint inhibitors in cancer patients: an observational, retrospective, pharmacovigilance study using the FAERS database.
    タグ:

    • FAERS
    2024/7/1

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