Literature DB >> 19851530

An atypical presentation of liver enzyme elevation resulting from bosentan use.

Kimberley Mulchey1, Zoheir Bshouty.   

Abstract

Hepatocellular enzyme elevation is a known side effect of both bosentan and atorvastatin. However, a rise in liver enzyme level not characteristic of either agent individually may represent a reaction to their combination or an atypical reaction to bosentan alone. The present case report describes a patient who had been taking atorvastatin for many years and was started on bosentan for chronic thromboembolic pulmonary hypertension. After 19 weeks of therapy, she developed severe liver enzyme elevation that necessitated the discontinuation of both bosentan and atorvastatin. Although the safety of reintroducing bosentan in such a case is unknown, it was reintroduced in this patient because of the severity of her disease, the demonstrated treatment benefit and the lack of alternative treatment options. On reintroduction of bosentan alone, she again demonstrated significant liver enzyme elevation - this time occurring after only two doses. The present case highlights that bosentan can cause more rapid and severe hepatocellular enzyme elevation than previously believed, thus necessitating more frequent monitoring.

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Year:  2009        PMID: 19851530      PMCID: PMC2779174          DOI: 10.1155/2009/958617

Source DB:  PubMed          Journal:  Can Respir J        ISSN: 1198-2241            Impact factor:   2.409


  6 in total

1.  Investigation of the mutual pharmacokinetic interactions between bosentan, a dual endothelin receptor antagonist, and simvastatin.

Authors:  Jasper Dingemanse; Dieter Schaarschmidt; Paul L M van Giersbergen
Journal:  Clin Pharmacokinet       Date:  2003       Impact factor: 6.447

Review 2.  Statins: mechanism of action and effects.

Authors:  C Stancu; A Sima
Journal:  J Cell Mol Med       Date:  2001 Oct-Dec       Impact factor: 5.310

3.  The endothelin antagonist bosentan inhibits the canalicular bile salt export pump: a potential mechanism for hepatic adverse reactions.

Authors:  K Fattinger; C Funk; M Pantze; C Weber; J Reichen; B Stieger; P J Meier
Journal:  Clin Pharmacol Ther       Date:  2001-04       Impact factor: 6.875

Review 4.  Clinical pharmacology of bosentan, a dual endothelin receptor antagonist.

Authors:  Jasper Dingemanse; Paul L M van Giersbergen
Journal:  Clin Pharmacokinet       Date:  2004       Impact factor: 6.447

Review 5.  Risk management strategies in the postmarketing period : safety experience with the US and European bosentan surveillance programmes.

Authors:  Eleanor S Segal; Cecile Valette; Laurence Oster; Luc Bouley; Catarina Edfjall; Peter Herrmann; Massimo Raineri; Mary Kempff; Saundra Beacham; Cinda van Lierop
Journal:  Drug Saf       Date:  2005       Impact factor: 5.606

6.  Ambrisentan for the treatment of pulmonary arterial hypertension: results of the ambrisentan in pulmonary arterial hypertension, randomized, double-blind, placebo-controlled, multicenter, efficacy (ARIES) study 1 and 2.

Authors:  Nazzareno Galiè; Horst Olschewski; Ronald J Oudiz; Fernando Torres; Adaani Frost; Hossein A Ghofrani; David B Badesch; Michael D McGoon; Vallerie V McLaughlin; Ellen B Roecker; Michael J Gerber; Christopher Dufton; Brian L Wiens; Lewis J Rubin
Journal:  Circulation       Date:  2008-05-27       Impact factor: 29.690

  6 in total
  1 in total

1.  Hepatic safety of ambrisentan alone and in combination with tadalafil: a post-hoc analysis of the AMBITION trial.

Authors:  Krishna R Patel; Christiana J Blair; James D Tislow
Journal:  Pulm Circ       Date:  2018-08-20       Impact factor: 3.017

  1 in total

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