Farmacologia do piroxicam

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The impact of uridine diphosphate—glucuronosyltransferase 1A9 UGT1A9 gene promoter region single-nucleotide polymorphisms T—A and C—T on early mycophenolic acid dose-interval exposure in de novo renal allograft recipients.

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The impact of uridine diphosphate—glucuronosyltransferase 1A9 UGT1A9 gene promoter region single-nucleotide polymorphisms T—A and C—T on early mycophenolic acid dose-interval exposure in de novo renal allograft recipients Next article in issue: Next article in issue: Abstract Objective Our objective was to evaluate the influence of cytochrome P CYP 2C9 polymorphisms on the pharmacokinetics and pharmacodynamics of the nonsteroidal anti-inflammatory drug piroxicam.

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Our objective was to evaluate the influence of cytochrome P CYP 2C9 polymorphisms on the pharmacokinetics and pharmacodynamics of the nonsteroidal anti-inflammatory drug piroxicam.

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Blood samples were collected at various time points up to hours for measurements of the concentrations of piroxicam and thromboxane B 2 TXB 2.

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