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• • Will the introduction of beta-lactamase inhibitors alter the adverse event profile of parent penicillins antibiotics? a pharmacovigilance study based on amoxicillin-clavulanate and ampicillin-sulbactam.
    タグ:

    • FAERS
    2026/3/30
  • Temsirolimus safety evaluation: real-world adverse event analysis from the FDA adverse event reporting system database.
    タグ:

    • FAERS
    2026/3/30
  • Vitiligo secondary to immunosuppressants: a pharmacovigilance study of the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2026/3/30
  • Comprehensive Study of Drug-Associated Severe Allergic Reactions: An Analysis of High-Risk Medications and Epidemiological Trends Based on the FAERS Database.
    タグ:

    • FAERS
    2026/3/31
  • A Disproportionality Analysis of Immune Checkpoint Inhibitors in Combination With Platinum-Based Agents Using the FDA Adverse Event Reporting System Database.
    タグ:

    • FAERS
    2026/3/31
  • Post-marketing safety signals of four JAK inhibitors for alopecia areata: an indication-restricted FAERS pharmacovigilance study.
    タグ:

    • FAERS
    2026/4/1
  • A real-world pharmacovigilance analysis of uveitis from systemic medications.
    タグ:

    • FAERS
    2026/4/1
  • Drug-induced fever: a pharmacovigilance analysis based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2026/4/1
  • Pharmacovigilance analysis of iodinated contrast media related respiratory adverse effects based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2026/4/1
  • Orphan drug propranolol for infantile hemangioma: ten-year real-world safety data from the FAERS database.
    タグ:

    • FAERS
    2026/4/2

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