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• • Drug-Related Hypertension: A Disproportionality Analysis Leveraging the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/3/11
  • Eosinophil-induced adverse events induced by treatment with programmed cell death 1/ligand 1 inhibitors: A comprehensive disproportionality analysis of the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/3/11
  • Comparative safety signals of dopamine agonists: psychiatric and cardiovascular risks derived from FDA adverse event reporting system (FAERS) data.
    タグ:

    • FAERS
    2025/3/11
  • Alopecia Associated With the Use of Immune Checkpoint Inhibitors: A Disproportionality Analysis Using the Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/3/11
  • Opposite causal effects of type 2 diabetes and metformin on Alzheimer’s disease.
    タグ:

    • FAERS
    2025/3/11
  • Adverse drug reactions to atezolizumab in combination with bevacizumab in hepatocellular carcinoma patients: an analysis of the food and drug administration adverse event reporting system database.
    タグ:

    • FAERS
    2025/3/10
  • Adverse events reporting of edaravone: a real-world analysis from FAERS database.
    タグ:

    • FAERS
    2025/3/10
  • A Disproportionality Analysis on Benzoyl Peroxide and Its Risk of Malignancy Using the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/3/10
  • Exploring Connections Between Weight-Loss Medications and Thyroid Cancer: A Look at the FDA Adverse Event Reporting System Database.
    タグ:

    • FAERS
    2025/3/9
  • A real-world pharmacovigilance study of omalizumab using disproportionality analysis in the FDA adverse drug events reporting system database.
    タグ:

    • FAERS
    2025/3/9

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