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Fibrates et risques thrombo-emboliques veineux : étude cas/non-cas dans la base nationale de pharmacovigilance

Authors :
Pascal Auriche
Marie-Blanche Valnet-Rabier
Antoine Coquerel
Annabelle Page
Marion Sassier
Xavier Humbert
Charles Dolladille
Elodie Sole
Emmanuelle Guitton
Sophie Fedrizzi
Joachim Alexandre
Thierry Vial
Source :
Therapies. 72:677-682
Publication Year :
2017
Publisher :
Elsevier BV, 2017.

Abstract

Summary Introduction Several studies have investigated the occurrence of venous thromboembolic events (phlebitis and pulmonary embolism) [VTE] and fibrates. Fibrates could be associated with VTE although published data are contradictory. The objective of this study is to confirm the link between VTE and fibrates. Materials and methods Retrospective disproportionality analysis (case/non-case method) from observations recorded consecutively in the French pharmacovigilance database between 1985 and 2016. Cases were defined as embolic and thrombotic events, thrombophlebitis; Non-cases were other adverse events reported over the same period. We measured the disproportionality of exposure to each fibrate among cases and no-cases. The analysis was validated with a positive control (drospirenone) and a negative control (paracetamol). Results We compared 19,436 cases (including 161 mentioning fibrates) to 563,310 non-cases (including 3228 fibrates). Reports of VTE were significantly associated with fenofibrate (ROR = 1.83; 95% CI = [1.53; 2.2]) but not with other fibrates: bezafibrate (ROR = 0.44; 95% CI = [0.2; 0.99]), ciprofibrate (ROR = 1.15; 95% CI = [0.76; 1.73]) and gemfibrozil (ROR = 0.91; 95% CI = [0.45; 1.84]). Conclusion With this study, we confirm the link between VTE and fenofibrate. It is therefore advisable to remain cautious when prescribing fenofibrate, in particular in case of past history of VTE and to declare systematically any venous thromboembolic adverse events observed with these drugs.

Details

ISSN :
00405957
Volume :
72
Database :
OpenAIRE
Journal :
Therapies
Accession number :
edsair.doi...........4e902f03efd0ac6ddbee99f4d8634864
Full Text :
https://doi.org/10.1016/j.therap.2017.07.002