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Assessment of adverse drug reaction reports related to pediatric patients sent to pharmacovigilance unit, Brazil

  • At: 2006 FIP Congress in Salvadore (Brazil)
  • Type: Poster
  • By: BITTENCOURT, Milena (Pharmacovigilance Unit/Nuvig/Anvisa, Brasilia, Brazil)
  • Co-author(s): Dias, Murilo (Pharmacovigilance Unit/Nuvig/Anvisa, Brasilia, Brazil)
    Silva, Leandro (Pharmacovigilance Unit/Nuvig/Anvisa, Brasilia, Brazil)
    Melo, José Romério (Pharmacovigilance Unit/Nuvig/Anvisa, Brasilia, Brazil)
    Figueiredo, Patrícia (Pharmacovigilance Unit/Nuvig/Anvisa, Brasilia, Brazil)
    Costa, Alessandra (Pharmacovigilance Unit/Nuvig/Anvisa, Brasilia, Brazil)
  • Abstract:

    Background: Few clinical trials select children as study population during a drug development, so adverse drug reactions (ADRs) related to pediatric patients become a concern to National System of Pharmacovigilance in Brazil. Lack of information about ADRs in children makes ADRs more difficult to be detected and reported by health professionals.
    Aim

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Last update 4 October 2019

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