• #31 A guide to reporting disproportionality analyses – Michele Fusaroli and Daniele Sartori

  • 2024/09/30
  • 再生時間: 43 分
  • ポッドキャスト

#31 A guide to reporting disproportionality analyses – Michele Fusaroli and Daniele Sartori

  • サマリー

  • Disproportionality analyses are a mainstay of pharmacovigilance research, but without clear guidelines, they often lead to confusion and misinterpretation. Enter the READUS-PV statement: the first-ever guide for reporting disproportionality analyses that are replicable, reliable, and reproducible.

    Tune in to find out:

    • The history of reporting guidelines in pharmacovigilance and why the READUS-PV guidelines were created
    • Why there has been a spike in the publication of disproportionality analyses in recent years and what this means for their reliability
    • What it means to publish “good” pharmacovigilance science


    Want to know more?

    • Read the READUS-PV guidelines, why they were created, and why they are important.
    • In 2021, Khouri and colleagues showed that current methods and models used for disproportionality analyses are unreliable, and Mouffak and colleagues found that there is a tendency to overstate results in published disproportionality analyses.
    • A book on data mining techniques in Pharmacovigilance by Poluzzi and colleagues delves deeper into this exponential increase in disproportionality analyses.
    • This paper elaborates on the Delphi technique, and how it is used to gather data from reviewers to achieve scientific consensus on a problem.

    Join the conversation on social media
    Follow us on X, LinkedIn, or Facebook and share your thoughts about the show with the hashtag #DrugSafetyMatters.

    Got a story to share?
    We’re always looking for new content and interesting people to interview. If you have a great idea for a show, get in touch!

    About UMC
    Read more about Uppsala Monitoring Centre and how we work to advance medicines safety.

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あらすじ・解説

Disproportionality analyses are a mainstay of pharmacovigilance research, but without clear guidelines, they often lead to confusion and misinterpretation. Enter the READUS-PV statement: the first-ever guide for reporting disproportionality analyses that are replicable, reliable, and reproducible.

Tune in to find out:

  • The history of reporting guidelines in pharmacovigilance and why the READUS-PV guidelines were created
  • Why there has been a spike in the publication of disproportionality analyses in recent years and what this means for their reliability
  • What it means to publish “good” pharmacovigilance science


Want to know more?

  • Read the READUS-PV guidelines, why they were created, and why they are important.
  • In 2021, Khouri and colleagues showed that current methods and models used for disproportionality analyses are unreliable, and Mouffak and colleagues found that there is a tendency to overstate results in published disproportionality analyses.
  • A book on data mining techniques in Pharmacovigilance by Poluzzi and colleagues delves deeper into this exponential increase in disproportionality analyses.
  • This paper elaborates on the Delphi technique, and how it is used to gather data from reviewers to achieve scientific consensus on a problem.

Join the conversation on social media
Follow us on X, LinkedIn, or Facebook and share your thoughts about the show with the hashtag #DrugSafetyMatters.

Got a story to share?
We’re always looking for new content and interesting people to interview. If you have a great idea for a show, get in touch!

About UMC
Read more about Uppsala Monitoring Centre and how we work to advance medicines safety.

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