HPS-193 - Automating adverse drug reaction (ADR) report analysis for enhanced risk mitigation

• At: Copenhagen (Denmark) (2025)
• Type: Poster
• Poster code: HPS-193
• By: LEOW, Jo Lene (Singapore Health Services, Singapore)
• Co-author(s): Dr Jo Lene Leow (Singapore Health Services, Singapore, Singapore)
  Ms Nurshazwani Zainol (Singapore Health Services, Singapore, Singapore)
  A/Prof Lita Chew (Singapore Health Services, Singapore, Singapore)
  Prof Lai Yun Ho (Singapore Health Services, Singapore, Singapore)
  
• Abstract:

  Background
  Adverse Drug Reaction (ADR) reporting is a cornerstone of pharmacovigilance, enabling the identification of drug safety concerns and the development of risk mitigation strategies. Traditional manual analysis of ADR reports is labour-intensive, error-prone, and difficult to scale, limiting the timeliness and effectiveness of safety..

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