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論文・技術情報

• • Drug Safety Signals for Pediatric Osteopenia and Osteoporosis: Disproportionality Analysis of USFDA Adverse Event Reporting System Analysis.
    タグ:

    • FAERS
    2025/5/26
  • Drug-related suicidal ideation in the K-12 population: a real-world pharmacovigilance study of the FDA adverse event reporting system (FAERS) database.
    タグ:

    • FAERS
    2025/5/25
  • Unveiling the hidden risks: analysis of adverse drug reactions associated with probiotics from the FAERS database – quality improvement study.
    タグ:

    • FAERS
    2025/5/28
  • Safety concerns of maternal antiseizure medications exposure on perinatal and offspring outcomes: a disproportionality analysis based on FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/5/28
  • A pharmacovigilance study on probiotic preparations based on the FDA Adverse Event Reporting System from 2005 to 2023.
    タグ:

    • FAERS
    2025/5/28
  • Real-World Safety Profile of Proton Pump Inhibitors in Infants as Reported in the FDA Adverse Event Reporting System (FAERS): Tiny Tummies, Key Decisions.
    タグ:

    • FAERS
    2025/5/28
  • Disproportionality Analysis of Renal Adverse Events Associated with a Combination of Immune Checkpoint Inhibitors and Acid-Suppressing Agents-A Pharmacovigilance Study Based on the FAERS Database.
    タグ:

    • FAERS
    2025/5/28
  • Evaluation of dermatologic adverse events associated with aromatase inhibitors: insights from the FAERS database.
    タグ:

    • FAERS
    2025/5/29
  • Sodium-glucose cotransporter-2 inhibitors and ketoacidosis in heart failure: analysis of US Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2025/5/29
  • Post-marketing safety of Lantus and its interchangeable biosimilar Semglee in the United States: A disproportionality analysis using the FDA Adverse Event Reporting System (FAERS) database.
    タグ:

    • FAERS
    2025/5/29

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