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• • Mortality and oral anticoagulants in the Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • KAERS
    • FAERS

    2017/8/2
  • Association between GvHD and nivolumab in the FDA adverse event reporting system.
    タグ:

    • FAERS

    2017/8/2
  • Discovering adverse drug events combining spontaneous reports with electronic medical records: a case study of conventional DMARDs and biologics for rheumatoid arthritis.
    タグ:

    • FAERS

    2017/8/18
  • Risk of Pancreatitis Following Treatment of Irritable Bowel Syndrome With Eluxadoline.
    タグ:

    • FAERS

    2017/8/15
  • Patient-relevant outcomes associated with generic tamsulosin, levothyroxine and amphetamine in the FDA Adverse Event Reporting System: a pilot study.
    タグ:

    • FAERS

    2017/7/8
  • Ketoacidosis associated with SGLT2 inhibitor treatment: Analysis of FAERS data.
    タグ:

    • FAERS

    2017/7/25
  • SGLT2 inhibitors and amputations in the US FDA Adverse Event Reporting System.
    タグ:

    • FAERS

    2017/7/25
  • Drug-induced gingival hyperplasia: a retrospective study using spontaneous reporting system databases.
    タグ:

    • JADER
    • FAERS

    2017/7/22
  • Proton Pump Inhibitors and the Risk for Fracture at Specific Sites: Data Mining of the FDA Adverse Event Reporting System.
    タグ:

    • FAERS

    2017/7/19
  • Accelerated approval of drugs: ethics versus efficacy.
    タグ:

    • FAERS

    2017/7/1

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