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Regulatory and pharmacological aspects of adverse drug reaction reporting: perspectives on pharmacists' impact and public health roles

  • In: G6 - Strengthening the responsible self care of patients on Wednesday, 5 September 2007, 13:00-16:00
  • At: Beijing (China) (2007)
  • Type: Presentation
  • By: SUBRAMANIAM, Vaiyapuri (U.S. Department of Veterans Affairs, Washington, DC, United States of America)
  • Abstract:

    The proliferation in the use of medicines has increased the risks posed by medication-related adverse drug events (ADE) resulting in adverse drug reactions (ADRs). An increased understanding of ADRs is essential to ensure the safe use of medicines. Access to ADE information from regulatory requirements and voluntary reporting and surveillance


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Last update 28 September 2023

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