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Cytochrome P450 3A Inhibition by Ketoconazole Affects Prasugrel and Clopidogrel Pharmacokinetics and Pharmacodynamics Differently

Clinical pharmacology and therapeutics, 2007-05, Vol.81 (5), p.735-741

2007

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Confidence interval criteria for assessment of dose proportionality

Pharmaceutical research, 2000-10, Vol.17 (10), p.1278-1283

2000

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Prasugrel pharmacokinetics and pharmacodynamics in subjects with moderate renal impairment and end-stage renal disease

Journal of clinical pharmacy and therapeutics, 2009-10, Vol.34 (5), p.585-594

2009

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Common polymorphisms of CYP2C19 and CYP2C9 affect the pharmacokinetic and pharmacodynamic response to clopidogrel but not prasugrel

Journal of thrombosis and haemostasis, 2007-12, Vol.5 (12), p.2429-2436

2007

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Comparison of formation of thiolactones and active metabolites of prasugrel and clopidogrel in rats and dogs

Xenobiotica, 2009-03, Vol.39 (3), p.218-226

2009

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Effect of rifampin on the pharmacokinetics and pharmacodynamics of prasugrel in healthy male subjects

Current medical research and opinion, 2009-08, Vol.25 (8), p.1821-1829

2009

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Disposition and metabolic fate of prasugrel in mice, rats, and dogs

Xenobiotica, 2007-08, Vol.37 (8), p.884-901

2007

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Pharmacokinetics and pharmacodynamics of prasugrel in subjects with moderate liver disease

Journal of clinical pharmacy and therapeutics, 2009-10, Vol.34 (5), p.575-583

2009

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Salt form selection and characterization of LY333531 mesylate monohydrate

International journal of pharmaceutics, 2000-04, Vol.198 (2), p.239-247

2000

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Comparison of mechanism-based inhibition of human cytochrome P450 2C19 by ticlopidine, clopidogrel, and prasugrel

Xenobiotica, 2009-11, Vol.39 (11), p.836-843

2009

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Absorption, distribution and excretion of the new thienopyridine agent prasugrel in rats

Xenobiotica, 2007-07, Vol.37 (7), p.788-801

2007

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Preclinical characterization of 2-[3-[3-[(5-ethyl-4'-fluoro-2-hydroxy[1,1'-biphenyl]-4-yl)oxy]propoxy]-2-propylphenoxy]benzoic acid metabolism: in vitro species comparison and in vivo disposition in rats

Drug metabolism and disposition, 2003-11, Vol.31 (11), p.1382-1390

2003

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Imidazoline Derivatives as Corrosion Inhibitors of Carbon Steel in Crude Oils and Associated Water

Energy sources. Part A, Recovery, utilization, and environmental effects, 2012-06, Vol.34 (15), p.1371-1383

2012

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Disposition of LY333531, a selective protein kinase C β inhibitor, in the Fischer 344 rat and beagle dog

Xenobiotica, 2002-11, Vol.32 (11), p.1045-1052

2002

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Clinical Pharmacology and Pharmacokinetics of Fluoxetine: A Review

British journal of psychiatry, 1988-09, Vol.153 (S3), p.47-50

1988

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Design of CMOS RF Doherty Power Amplifier in Low-Power 5G Wireless Networks for IoT Application

2023 IEEE 11th Conference on Systems, Process & Control (ICSPC), 2023, p.310-314

2023

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Metabolism and Disposition of the Thienopyridine Antiplatelet Drugs Ticlopidine, Clopidogrel, and Prasugrel in Humans

Journal of clinical pharmacology, 2010-02, Vol.50 (2), p.126-142

2010

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Fluoxetine: clinical pharmacology and physiologic disposition

The journal of clinical psychiatry, 1985-03, Vol.46 (3 Pt 2), p.14

1985

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Characterisation of natural rubber waste for pyrolysis

Plastics, rubber & composites, 2000-08, Vol.29 (8), p.427-432

2000

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Stereoselective disposition of the enantiomers of the benzoquinolinone LY191704, a human type I 5 alpha-reductase inhibitor. Differences between rats and dogs

Drug metabolism and disposition, 1996-10, Vol.24 (10), p.1162

1996

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Speckle Cross-Correlation Method in Measuring Fine Surface Displacements

Journal of atomic and molecular physics, 2012-01, Vol.2012 (2012), p.1-6

2012

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Effects of the Proton Pump Inhibitor Lansoprazole on the Pharmacokinetics and Pharmacodynamics of Prasugrel and Clopidogrel

Journal of clinical pharmacology, 2008-04, Vol.48 (4), p.475-484

2008

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Strengthening State Security Function For The State Sovereignty In Immigration Perspective (Strengthening State's Security of Immigration Function for the State Sovereignty)

Jurnal Ad'ministrare, 2022-11, Vol.9 (2), p.431

N. A, Farid Asyam

2022

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Interactions of two major metabolites of prasugrel, a thienopyridine antiplatelet agent, with the cytochromes P450

Drug metabolism and disposition, 2006-04, Vol.34 (4), p.600-607

2006

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Tc-99m labeled leukocytes: preparation and use in identification of abscess and tissue rejection

Radiology, 1983-09, Vol.148 (3), p.827-831

1983

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Cytochrome P450 3A Inhibition by Ketoconazole Affects Prasugrel and Clopidogrel Pharmacokinetics and Pharmacodynamics Differently

Confidence interval criteria for assessment of dose proportionality

Prasugrel pharmacokinetics and pharmacodynamics in subjects with moderate renal impairment and end-stage renal disease

Common polymorphisms of CYP2C19 and CYP2C9 affect the pharmacokinetic and pharmacodynamic response to clopidogrel but not prasugrel

Comparison of formation of thiolactones and active metabolites of prasugrel and clopidogrel in rats and dogs

Effect of rifampin on the pharmacokinetics and pharmacodynamics of prasugrel in healthy male subjects

Disposition and metabolic fate of prasugrel in mice, rats, and dogs

Pharmacokinetics and pharmacodynamics of prasugrel in subjects with moderate liver disease

Salt form selection and characterization of LY333531 mesylate monohydrate

Comparison of mechanism-based inhibition of human cytochrome P450 2C19 by ticlopidine, clopidogrel, and prasugrel

Absorption, distribution and excretion of the new thienopyridine agent prasugrel in rats

Preclinical characterization of 2-[3-[3-[(5-ethyl-4'-fluoro-2-hydroxy[1,1'-biphenyl]-4-yl)oxy]propoxy]-2-propylphenoxy]benzoic acid metabolism: in vitro species comparison and in vivo disposition in rats

Imidazoline Derivatives as Corrosion Inhibitors of Carbon Steel in Crude Oils and Associated Water

Disposition of LY333531, a selective protein kinase C β inhibitor, in the Fischer 344 rat and beagle dog

Clinical Pharmacology and Pharmacokinetics of Fluoxetine: A Review

Design of CMOS RF Doherty Power Amplifier in Low-Power 5G Wireless Networks for IoT Application

Metabolism and Disposition of the Thienopyridine Antiplatelet Drugs Ticlopidine, Clopidogrel, and Prasugrel in Humans

Fluoxetine: clinical pharmacology and physiologic disposition

Characterisation of natural rubber waste for pyrolysis

Stereoselective disposition of the enantiomers of the benzoquinolinone LY191704, a human type I 5 alpha-reductase inhibitor. Differences between rats and dogs

Speckle Cross-Correlation Method in Measuring Fine Surface Displacements

Effects of the Proton Pump Inhibitor Lansoprazole on the Pharmacokinetics and Pharmacodynamics of Prasugrel and Clopidogrel

Strengthening State Security Function For The State Sovereignty In Immigration Perspective (Strengthening State's Security of Immigration Function for the State Sovereignty)

Interactions of two major metabolites of prasugrel, a thienopyridine antiplatelet agent, with the cytochromes P450

Tc-99m labeled leukocytes: preparation and use in identification of abscess and tissue rejection

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