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Results of an adverse drug events monitoring program conducted by pharmacists in a brazilian teaching hospital

  • At: 2006 FIP Congress in Salvadore (Brazil)
  • Type: Poster
  • By: SOUSA, Altamir (Universidade de São Paulo, Serviço de Farmácia, Sao Paulo, Brazil)
  • Co-author(s): Yamaguchi, Alice (Universidade de São Paulo, SAO PAULO, Brazil)
    Rodrigues, Carlos (Universidade de São Paulo, SAO PAULO, Brazil)
    Takagi, Cristina (Universidade de São Paulo, SAO PAULO, Brazil)
    Ribeiro, Eliane (Universidade de São Paulo, SAO PAULO, Brazil)
    Sugawara, Emília (Universidade de São Paulo, SAO PAULO, Brazil)
    Franca, Gustavo (Universidade de São Paulo, SAO PAULO, Brazil)
    Sakai, Maria (Universidade de São Paulo, SAO PAULO, Brazil)
    Lima, Maria (Universidade de São Paulo, SAO PAULO, Brazil)
    Ricci, Monica (Universidade de São Paulo, SAO PAULO, Brazil)
    Takahashi, Patrícia (Universidade de São Paulo, SAO PAULO, Brazil)
    Brassica, Sandra (Universidade de São Paulo, SAO PAULO, Brazil)
  • Abstract:

    INTRODUCTION/OBJECTIVE

    The University Hospital of University of São Paulo (HU/USP) is one of the monitoring centers of The National Pharmacovigilance System developed by the Brazilian drug regulatory agency (Anvisa). The main purpose of this study was to demonstrate our institutional experience in reporting adverse drug reactions (ADRs) from..

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Last update 4 October 2019

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