Optimising resources for international safety data collection and analysis

• In: 3A - Reporting of adverse events and errors on Friday, 5 October 2012, 09:00-12:00
• At: Amsterdam (the Netherlands) (2012)
• Type: Presentation
• By: LINDQUIST, Marie (Uppsala Monitoring Centre, Uppsala, Sweden)
• Abstract:

  The original aim of pharmacovigilance - to identify previously unknown suspected adverse reactions, mainly to new drug products - covers only a small part of the disease burden related to the use of medicines. Only a broader, holistic look at all the factors leading to adverse patient outcomes on medication will reduce the resulting global

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