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• • Post-marketing safety concerns with lecanemab: a pharmacovigilance study based on the FDA Adverse Event Reporting System database.
    タグ:

    • FAERS

    2025/1/9
  • Pharmacovigilance study of the association between progestogen and depression based on the FDA adverse event reporting System (FAERS).
    タグ:

    • FAERS

    2025/1/9
  • A Real-World Pharmacovigilance Study of FDA Adverse Event Reporting System Events for Obeticholic Acid.
    タグ:

    • FAERS

    2025/1/8
  • Real world pharmacovigilance assessment of drug related macular degeneration risks.
    タグ:

    • FAERS

    2025/1/8
  • Interaction between dipeptidyl-peptidase-4 inhibitors and drugs acting on renin angiotensin aldosterone system for the risk of angioedema: a pharmacovigilance assessment using disproportionality and interaction analyses.
    タグ:

    • FAERS

    2025/1/8
  • Adverse Events Associated with Antivirals for COVID-19: An Analysis Based on FDA Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS

    2025/1/8
  • Hematological toxicities in antibody-drug conjugates related with breast cancer: a pharmacovigilance study using FDA adverse event reporting system database.
    タグ:

    • FAERS

    2025/1/8
  • Safety Evaluation of the Combination with Dexrazoxane and Anthracyclines: A Disproportionality Analysis Based on the Food and Drug Administration Adverse Event Reporting System Database.
    タグ:

    • FAERS

    2025/1/8
  • Drug Safety During Breastfeeding: A Comparative Analysis of FDA Adverse Event Reports and LactMed((R)).
    タグ:

    • FAERS

    2025/1/8
  • IL-6R Inhibitors and Gastrointestinal Perforations: A Pharmacovigilance Study and a Predicting Nomogram.
    タグ:

    • FAERS

    2025/1/8

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