SIMVASTATIN-INDUCED RHABDOMYOLYSIS IN A HEART-TRANSPLANT RECIPIENT RECEIVING CYCLOSPORINE
被引:14
作者:
BLAISON, G
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机构:
CHU STRASBOURG,SERV MED INTERNE A,UNITE IMMUNOPATHOL,F-67091 STRASBOURG,FRANCECHU STRASBOURG,SERV MED INTERNE A,UNITE IMMUNOPATHOL,F-67091 STRASBOURG,FRANCE
BLAISON, G
[1
]
WEBER, JC
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CHU STRASBOURG,SERV MED INTERNE A,UNITE IMMUNOPATHOL,F-67091 STRASBOURG,FRANCECHU STRASBOURG,SERV MED INTERNE A,UNITE IMMUNOPATHOL,F-67091 STRASBOURG,FRANCE
WEBER, JC
[1
]
SACHS, D
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CHU STRASBOURG,SERV MED INTERNE A,UNITE IMMUNOPATHOL,F-67091 STRASBOURG,FRANCECHU STRASBOURG,SERV MED INTERNE A,UNITE IMMUNOPATHOL,F-67091 STRASBOURG,FRANCE
SACHS, D
[1
]
KORGANOW, AS
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CHU STRASBOURG,SERV MED INTERNE A,UNITE IMMUNOPATHOL,F-67091 STRASBOURG,FRANCECHU STRASBOURG,SERV MED INTERNE A,UNITE IMMUNOPATHOL,F-67091 STRASBOURG,FRANCE
KORGANOW, AS
[1
]
MARTIN, T
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CHU STRASBOURG,SERV MED INTERNE A,UNITE IMMUNOPATHOL,F-67091 STRASBOURG,FRANCECHU STRASBOURG,SERV MED INTERNE A,UNITE IMMUNOPATHOL,F-67091 STRASBOURG,FRANCE
MARTIN, T
[1
]
KRETZ, JG
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CHU STRASBOURG,SERV MED INTERNE A,UNITE IMMUNOPATHOL,F-67091 STRASBOURG,FRANCECHU STRASBOURG,SERV MED INTERNE A,UNITE IMMUNOPATHOL,F-67091 STRASBOURG,FRANCE
KRETZ, JG
[1
]
PASQUALI, JL
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CHU STRASBOURG,SERV MED INTERNE A,UNITE IMMUNOPATHOL,F-67091 STRASBOURG,FRANCECHU STRASBOURG,SERV MED INTERNE A,UNITE IMMUNOPATHOL,F-67091 STRASBOURG,FRANCE
PASQUALI, JL
[1
]
机构:
[1] CHU STRASBOURG,SERV MED INTERNE A,UNITE IMMUNOPATHOL,F-67091 STRASBOURG,FRANCE
来源:
REVUE DE MEDECINE INTERNE
|
1992年
/
13卷
/
01期
关键词:
RHABDOMYOLYSIS;
UNDESIRABLE DRUG EFFECTS;
HEART TRANSPLANTATION;
SIMVASTATIN;
D O I:
10.1016/S0248-8663(05)80013-X
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Hydroxymethylglutaryl coenzyme A (HMG-CoA) reductase inhibitors are cholesterol-lowering agents which may induce rhabdomyolysis. The authors present a case of rhabdomyolysis attributed to simvastatin in a heart-transplant recipient. They stress the probability of a dose-dependent muscular toxicity and the risk of overdosage in patients already under treatment with drugs that interfere with the pharmacokinetics of HMG-CoA reductase inhibitors, notably ciclosporine.