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Off-label use of nicardipine as tocolytic and acute pulmonary oedema: a post-marketing analysis of adverse drug reaction reports in EudraVigilance.
Melis, Mauro; Cupelli, Amelia; Sottosanti, Laura; Buccellato, Elena; Biagi, Chiara; Vaccheri, Alberto; Motola, Domenico.
Afiliação
  • Melis M; Department of Medical and Surgical Sciences - Unit of Pharmacology, University of Bologna, Bologna, Italy.
  • Cupelli A; Italian Medicines Agency (Agenzia Italiana del Farmaco, AIFA)Pharmacovigilance Office, Rome, Italy.
  • Sottosanti L; Italian Medicines Agency (Agenzia Italiana del Farmaco, AIFA)Pharmacovigilance Office, Rome, Italy.
  • Buccellato E; Department of Medical and Surgical Sciences - Unit of Pharmacology, University of Bologna, Bologna, Italy.
  • Biagi C; Department of Medical and Surgical Sciences - Unit of Pharmacology, University of Bologna, Bologna, Italy.
  • Vaccheri A; Department of Medical and Surgical Sciences - Unit of Pharmacology, University of Bologna, Bologna, Italy.
  • Motola D; Department of Medical and Surgical Sciences - Unit of Pharmacology, University of Bologna, Bologna, Italy.
Pharmacoepidemiol Drug Saf ; 24(11): 1220-4, 2015 Nov.
Article em En | MEDLINE | ID: mdl-25845714
ABSTRACT

PURPOSE:

To evaluate a signal of acute pulmonary oedema (APO) due to nicardipine used off-label as tocolytic in pregnant women.

METHODS:

All the suspected cases of APO recorded in EudraVigilance database up to 31/01/2013 and associated with nicardipine containing medicinal products were retrieved. The Proportional Reporting Ratio was considered as measure of disproportionality. Individual cases evaluation was conducted.

RESULTS:

Thirty-four spontaneous cases regarding pregnancy women who experienced APO following nicardipine treatment as tocolytic were collected. The detected proportional reporting ratio was 50.96 (95% confidence interval lower bound equal to 36.75). The analysis focused on 10 serious cases. Most women, aged between 27 and 39 years, were treated with intravenous nicardipine. The most of the suspected adverse reactions occurred between 24 and 96 hours.

CONCLUSIONS:

A potentially causal association between APO and off-label use of nicardipine as tocolytic has been detected during a periodic signal detection activity. The Pharmacovigilance Risk Assessment Committee confirmed our findings, recommending an update of the summary of the product characteristics for medicines containing nicardipine for both intravenous and oral formulations. Then European Medicines Agency reaffirmed that nicardipine use in other indications is no longer recommended.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Edema Pulmonar / Nicardipino / Tocolíticos / Uso Off-Label Tipo de estudo: Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Edema Pulmonar / Nicardipino / Tocolíticos / Uso Off-Label Tipo de estudo: Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Ano de publicação: 2015 Tipo de documento: Article