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• • Safety Profile of Molnupiravir in the Treatment of COVID-19: A Descriptive Study Based on FAERS Data.
    タグ:

    • FAERS

    2023/1/9
  • Risk of Lichen Sclerosus and Lichen Planus in Patients Receiving Immune Checkpoint Inhibitors.
    タグ:

    • FAERS

    2023/1/9
  • Post-Marketing Safety of Vemurafenib: A Real-World Pharmacovigilance Study of the FDA Adverse Event Reporting System.
    タグ:

    • FAERS

    2023/1/8
  • Interstitial pneumonitis associated with combined regimen of immunotherapy and conventional therapies-pharmacovigilance database analysis with real-world data validation.
    タグ:

    • FAERS

    2023/1/5
  • Pharmacovigilance of triazole antifungal agents: Analysis of the FDA adverse event reporting system (FAERS) database.
    タグ:

    • FAERS

    2023/1/3
  • A post-marketing pharmacovigilance study of avapritinib: adverse event data mining and analysis based on the United States Food and Drug Administration Adverse Event Reporting System database.
    タグ:

    • FAERS

    2023/1/27
  • Hyperuricaemia, gout and related adverse events associated with antihypertensive drugs: A real-world analysis using the FDA adverse event reporting system.
    タグ:

    • FAERS

    2023/1/27
  • Analysis of Clinical Factors in Olaparib-related Anemia Using Adverse Drug Event Reporting Databases.
    タグ:

    • FAERS
    • JADER

    2023/1/26
  • Analysis of drug-induced liver-related adverse event trend reporting between 1997 and 2019.
    タグ:

    • FAERS
    • JADER

    2023/1/22
  • Evidence of Accidental Dosing Errors with Immediate-Release Sodium Oxybate: Data from the US Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS

    2023/1/21

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