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Assessment of adverse drug reaction reports related to pediatric patients sent to pharmacovigilance unit, Brazil
- In: SIG Pharmacoeconomics/Pharmacoepidemiology - Poster Session
- At: Salvadore (Brazil) (2006)
- Type: Poster
- Poster code: PP-P-020
- 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.
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Last update 28 September 2023