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論文・技術情報

• • Post-market safety profile and suicide risk signals of vortioxetine: a real-world pharmacovigilance study.
    タグ:

    • FAERS
    2026/5/1
  • Antibiotic-associated encephalopathy: A retrospective pharmacovigilance study based on 21 years of data from the US FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2026/5/4
  • Safety evaluation of finerenone and identification of factors contributing to nephrotoxicity: re-analysis using FDA adverse event reporting system data.
    タグ:

    • FAERS
    2026/5/3
  • Identifying Sex Differences in Adverse Events Reported on Opioid Drugs in the FDA’s Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2026/5/4
  • Cardiovascular Risks of COVID-19 Therapeutics: Integrated Analysis of FAERS, Electronic Health Records, and Transcriptomics.
    タグ:

    • FAERS
    2026/5/4
  • Signal Detection of Adverse Events Associated with Four Dihydropyridine Calcium Channel Blockers Based on the FAERS Database.
    タグ:

    • FAERS
    2026/5/4
  • Drug- and patient-specific neurological risk profiles of alpha1-adrenergic blockers: evidence from FAERS and external validation in JADER.
    タグ:

    • JADER
    • FAERS
    2026/5/4
  • The Cardiovascular Safety of Antiparkinsonian Drugs-Analysis of Signals in the FDA Adverse Event Report System Database.
    タグ:

    • FAERS
    2026/5/4
  • Adverse event of ACE inhibitors: A descriptive analysis of FAERS data.
    タグ:

    • FAERS
    2026/5/4
  • Kidney adverse events associated with calcineurin inhibitors: a real-world study based on the FAERS database and network pharmacology.
    タグ:

    • FAERS
    2026/5/4

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