Your browser doesn't support javascript.
loading
Systemic quinolones and risk of acute liver failure I: Analysis of data from the US FDA adverse event reporting system.
Taher, Mohamed Kadry; Alami, Abdallah; Gravel, Christopher A; Tsui, Derek; Bjerre, Lise M; Momoli, Franco; Mattison, Donald R; Krewski, Daniel.
Afiliação
  • Taher MK; McLaughlin Centre for Population Health Risk Assessment, Faculty of Medicine University of Ottawa Ottawa ON Canada.
  • Alami A; School of Epidemiology and Public Health University of Ottawa Ottawa ON Canada.
  • Gravel CA; Risk Sciences International Ottawa ON Canada.
  • Tsui D; Risk Sciences International Ottawa ON Canada.
  • Bjerre LM; McLaughlin Centre for Population Health Risk Assessment, Faculty of Medicine University of Ottawa Ottawa ON Canada.
  • Momoli F; School of Epidemiology and Public Health University of Ottawa Ottawa ON Canada.
  • Mattison DR; Department of Epidemiology, Biostatistics and Occupational Health McGill University Montreal QC Canada.
  • Krewski D; Risk Sciences International Ottawa ON Canada.
JGH Open ; 5(7): 778-784, 2021 Jul.
Article em En | MEDLINE | ID: mdl-34263072
ABSTRACT
BACKGROUND AND

AIM:

Quinolones are a potent and globally popular group of antibiotics that are used to treat a wide range of infections. Some case reports have raised concern about their possible association with acute hepatic failure (AHF). Data from the US FDA Adverse Event Reporting System were evaluated for signals of AHF in association with systemically administered quinolone antibiotics.

METHODS:

AHF reports between 1969 and 2019q2, with a focus on 2010-2019q2, were analyzed. Specifically, AHF reports linked to non-quinolone antibiotics of known hepatotoxicity were compared to reports with non-quinolone, non-hepatotoxic (reference) antibiotics; and AHF reports with quinolones were also compared to reports with the same group of reference antibiotics. Two disproportionality signal detection techniques (proportional reporting ratio, PRR, and empirical Bayes geometric mean, EBGM) were used to assess the AHF signal for both analyses.

RESULTS:

Only ciprofloxacin showed a marginal and significant AHF signal (PRR 1.85 [1.21, 2.81]; EBGM 1.54 [1.06, 1.81]); moxifloxacin, levofloxacin, and ofloxacin showed weak and nonsignificant signals.

CONCLUSION:

Further pharmacovigilance studies are required to confirm the association between ciprofloxacin and AHF seen in the present analysis.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Risk_factors_studies Idioma: En Revista: JGH Open Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Risk_factors_studies Idioma: En Revista: JGH Open Ano de publicação: 2021 Tipo de documento: Article