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[Adverse drug reactions in pediatrics: Experience of a regional pharmacovigilance center]. / Les effets indésirables médicamenteux en pédiatrie : expérience d'un centre régional de pharmacovigilance.
Saint-Martin, Caroline; Kanagaratnam, Lukshe; de Boissieu, Paul; Azzouz, Brahim; Abou Taam, Malak; Trenque, Thierry.
Afiliação
  • Saint-Martin C; Centre régional de pharmacovigilance et de pharmaco-épidémiologie de Champagne-Ardenne, CHU de Reims, 51092 Reims, France.
  • Kanagaratnam L; Unité d'aide méthodologique, pôle recherche et innovations, CHU de Reims, 51092 Reims, France; EA 3797, faculté de médecine, université de Reims Champagne-Ardenne, 51100 Reims, France.
  • de Boissieu P; Centre régional de pharmacovigilance et de pharmaco-épidémiologie de Champagne-Ardenne, CHU de Reims, 51092 Reims, France; EA 3797, faculté de médecine, université de Reims Champagne-Ardenne, 51100 Reims, France.
  • Azzouz B; Centre régional de pharmacovigilance et de pharmaco-épidémiologie de Champagne-Ardenne, CHU de Reims, 51092 Reims, France.
  • Abou Taam M; Centre régional de pharmacovigilance et de pharmaco-épidémiologie de Champagne-Ardenne, CHU de Reims, 51092 Reims, France; EA 3797, faculté de médecine, université de Reims Champagne-Ardenne, 51100 Reims, France.
  • Trenque T; Centre régional de pharmacovigilance et de pharmaco-épidémiologie de Champagne-Ardenne, CHU de Reims, 51092 Reims, France; EA 3797, faculté de médecine, université de Reims Champagne-Ardenne, 51100 Reims, France. Electronic address: ttrenque@chu-reims.fr.
Therapie ; 71(5): 467-473, 2016 Oct.
Article em Fr | MEDLINE | ID: mdl-27203165
ABSTRACT

AIM:

To describe the adverse drug reactions (ADR) and the drugs involved in pediatrics.

METHODS:

An observational study on all ADR notifications recorded in the French pharmacovigilance database by the Regional Pharmacovigilance Center of Champagne-Ardenne between 1 January 1985 and 31 December 2014 involving children from 0 to 17 years inclusive was performed. For all notifications, we studied the patient and the ADR characteristics.

RESULTS:

During the study period, 632 notifications were collected. The most frequently reported ATC (anatomical, therapeutic and chemical) classes were vaccines (15.9%), antineoplastics (12%) and antibiotics (11.1%). Forty-six percent of the notifications were serious. For serious ADRs, the most involved drugs were paracetamol, asparaginase and ibuprofen. Skin reactions were the most often reported ADRs. The most common lowest level terms (LLT) were urticaria (4.9%), hypersensitivity (4.1%), fever (2.9%) and vomiting (2.8%).

CONCLUSION:

ADR reporting to the pharmacovigilance system, in particular pediatric ADRs, should be encouraged. Information on the use of medicinal products, especially on self-medication use, need to be improve.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sistemas de Notificação de Reações Adversas a Medicamentos / Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos Tipo de estudo: Observational_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn País/Região como assunto: Europa Idioma: Fr Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sistemas de Notificação de Reações Adversas a Medicamentos / Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos Tipo de estudo: Observational_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn País/Região como assunto: Europa Idioma: Fr Ano de publicação: 2016 Tipo de documento: Article