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• • A comparative analysis of drug-induced kidney injury adverse reactions between cyclosporine and tacrolimus based on the FAERS database.
    タグ:

    • FAERS
    2025/5/3
  • Biomaterial-based drug delivery: evaluating the safety profiles of liposomal Vyxeos.
    タグ:

    • FAERS
    2025/5/2
  • Post-marketing Safety Evaluation of Lutathera ( 177 Lu-DOTATATE) : A Pharmacovigilance Analysis of FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/5/1
  • Drug-induced pancreatitis: a real-world analysis of the FDA Adverse Event Reporting System and network pharmacology.
    タグ:

    • FAERS
    2025/5/1
  • A real-world pharmacovigilance study of efgartigimod alfa in the FDA adverse event reporting system database.
    タグ:

    • FAERS
    2025/5/1
  • FAERS based disproportionality analysis and network pharmacology investigation of taxanes associated drug induced liver injury.
    タグ:

    • FAERS
    2025/5/1
  • Disproportionality analysis of ALK inhibitor-induced hemolytic adverse events: a pharmacovigilance study using the FDA Adverse Event Reporting System Database.
    タグ:

    • FAERS
    2025/4/30
  • Neurological adverse events associated with baclofen: A disproportionality analysis based on FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/4/30
  • Pulmonary adverse events associated with monoclonal antibodies approved for multiple myeloma: a pharmacovigilance study based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/4/30
  • Risk of thromboembolic events in patients co-treated with factor Xa-inhibiting direct oral anticoagulants and anti-seizure medications: insights from pharmacovigilance data.
    タグ:

    • FAERS
    2025/4/30

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