Simvastatin-associated rhabdomyolysis after coadministration of macrolide antibiotics in two patients
- PMID: 17381388
- DOI: 10.1592/phco.27.4.603
Simvastatin-associated rhabdomyolysis after coadministration of macrolide antibiotics in two patients
Abstract
Two men, aged 83 and 78 years, who received stable therapy with simvastatin 80 mg/day were hospitalized 1-2 weeks after completion of short-term treatment with erythromycin and clarithromycin, respectively. Both patients were admitted with myalgia, muscle weakness, functional disability (inability to raise arms and legs), and serum creatine kinase levels more than 60 times the upper limit of normal (ULN). Substantial elevations in aspartate aminotransferase (> 30 times the ULN) and alanine aminotransferase (> 7 times the ULN) levels were also observed. Rhabdomyolysis was diagnosed in both patients. Both recovered, but the combined events resulted in almost 40 days of hospitalization, the cost of which is considerable. According to the Naranjo adverse drug reaction probability scale, the likelihood that the rhabdomyolysis was secondary to a simvastatin-macrolide interaction was probable. Four cases of rhabdomyolysis after therapy with combined simvastatin and clarithromycin have been reported previously, but this is apparently the first report of rhabdomyolysis after coadministration of erythromycin. The interacting mechanism likely was inhibited cytochrome P450 (CYP) 3A4 metabolism and possibly P-glycoprotein transport of simvastatin as well. Previous reports of simvastatin-clarithromycin-related events involved additional drugs that inhibited CYP3A4 and P-glycoprotein. However, this was not the situation with our two patients. To prevent future events, it is crucial that clinicians recognize the interaction risk associated with concurrent use of simvastatin and clarithromycin or erythromycin. The risk could be managed by temporary interruption of simvastatin treatment or administration of a noninteracting antimicrobial agent.
Similar articles
-
Rhabdomyolysis associated with concomitant use of simvastatin and clarithromycin.Ann Pharmacother. 2004 Apr;38(4):719. doi: 10.1345/aph.1D243. Epub 2004 Feb 13. Ann Pharmacother. 2004. PMID: 14966253 No abstract available.
-
Rhabdomyolysis in association with simvastatin and amiodarone.Ann Pharmacother. 2004 Jun;38(6):978-81. doi: 10.1345/aph.1D498. Epub 2004 Apr 6. Ann Pharmacother. 2004. PMID: 15069169
-
Rhabdomyolysis in association with simvastatin and dosage increment in clarithromycin.Intern Med J. 2014 Jul;44(7):690-3. doi: 10.1111/imj.12464. Intern Med J. 2014. PMID: 25041770
-
Rhabdomyolysis secondary to a drug interaction between simvastatin and clarithromycin.Ann Pharmacother. 2001 Jan;35(1):26-31. doi: 10.1345/aph.10177. Ann Pharmacother. 2001. PMID: 11197581 Review.
-
Statin safety and drug interactions: clinical implications.Am J Cardiol. 2006 Apr 17;97(8A):27C-31C. doi: 10.1016/j.amjcard.2005.12.007. Epub 2006 Jan 25. Am J Cardiol. 2006. PMID: 16581325 Review.
Cited by
-
Pharmacokinetic comparison of the potential over-the-counter statins simvastatin, lovastatin, fluvastatin and pravastatin.Clin Pharmacokinet. 2008;47(7):463-74. doi: 10.2165/00003088-200847070-00003. Clin Pharmacokinet. 2008. PMID: 18563955 Review.
-
A Real-world Toxicity Atlas Shows that Adverse Events of Combination Therapies Commonly Result in Additive Interactions.Clin Cancer Res. 2024 Apr 15;30(8):1685-1695. doi: 10.1158/1078-0432.CCR-23-0914. Clin Cancer Res. 2024. PMID: 38597991 Free PMC article.
-
A Population-Based Study of Simvastatin Drug-Drug Interactions in Cardiovascular Disease Patients.AMIA Jt Summits Transl Sci Proc. 2020 May 30;2020:664-673. eCollection 2020. AMIA Jt Summits Transl Sci Proc. 2020. PMID: 32477689 Free PMC article.
-
Rhabdomyolysis caused by co-medication with simvastatin and clarithromycin.J Neurol. 2009 Jul;256(7):1182-3. doi: 10.1007/s00415-009-5078-6. Epub 2009 Mar 1. J Neurol. 2009. PMID: 19252767 No abstract available.
-
Potential statin-drug interactions: prevalence and clinical significance.Springerplus. 2014 Mar 31;3:168. doi: 10.1186/2193-1801-3-168. eCollection 2014. Springerplus. 2014. PMID: 24790817 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical