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Analysis of an adverse drug reporting surveillance

  • At: 2005 FIP Congress in Cairo (Egypt)
  • Type: Poster
  • By: TSAI (Chang Gung Memorial Hospital, Department of Pharmacy, Taoyuen Hsien, China Taiwan)
  • Co-author(s): Chan (Chang Gung Memorial Hospital, Taoyuen Hsien, China Taiwan)
    Chou (Chang Gung Memorial Hospital, Taoyuen Hsien, China Taiwan)
  • Abstract:

    Aim: Both the effective spontaneous reporting of adverse drug reactions (ADRs) and the rapid identification of possible drug safety hazards are important to pharmacovigilance. This study is describing an current electronic ADR-reporting system involves several approaches in which care-providers are encouraged to report adverse events via the

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Last update 4 October 2019

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