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handle: 10400.17/711
The authors report a clinical case of warfarin hypersensitivity noticed when a patient, with thromboembolic risk, was submitted to warfarin. She was found to be heterozigotic to -1639G>A (gene VKORC1) and homozygotic to 1075A>C (genotype CYP2C9*3/*3). In this article the warfarin pharmacodinamics and its role over Vitamin K is revisited. It includes some suggested indications for investigating genetic polymorphisms, in order to avoid complications associated with warfarin.
Varfarina, Medicine (General), R5-920, MAC MED MAF, R, Medicine, Efeitos Adversos, Anticoagulantes, Hipersensibilidade
Varfarina, Medicine (General), R5-920, MAC MED MAF, R, Medicine, Efeitos Adversos, Anticoagulantes, Hipersensibilidade
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