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Brasília méd ; 50(3)maio - 10 - 2014.
Article in Portuguese | LILACS-Express | LILACS | ID: lil-702926

ABSTRACT

Com o aumento do número de reações adversas a medicamentos, faz-se necessária a monitorização adequada dos medicamentos durante seu desenvolvimento e após a comercialização, papel desempenhado pela farmacovigilância.


It was observed that none of the documents investigated dealt with the search for adverse reactions to drugs during all the stages of clinical research. Theauthors explored these reactions only in phase IV or pharmacovigilance.

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