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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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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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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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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

2006

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Toward Energy-Efficient and Trustworthy eHealth Monitoring System

China communications, 2015, Vol.12 (1), p.46-65

2015

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The Platelet Inhibitory Effects and Pharmacokinetics of Prasugrel After Administration of Loading and Maintenance Doses in Healthy Subjects

Journal of cardiovascular pharmacology, 2006-03, Vol.47 (3), p.377-384

2006

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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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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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Switching directly to prasugrel from clopidogrel results in greater inhibition of platelet aggregation in aspirin-treated subjects

Platelets (Edinburgh), 2008-01, Vol.19 (4), p.275-281

2008

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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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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

2003

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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

Volltextzugriff (PDF)

Disposition of LY333531, a selective protein kinase C g 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

Volltextzugriff (PDF)

Characterisation of natural rubber waste for pyrolysis

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

2000

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Thermochemical processing of rubber waste to liquid fuel

Plastics, rubber & composites, 2000-02, Vol.29 (2), p.100-104

2000

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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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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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Single-Dose and Steady-State Pharmacokinetics of Tomoxetine in Normal Subjects

Journal of clinical pharmacology, 1985-05, Vol.25 (4), p.296-301

1985

Volltextzugriff (PDF)

Liquid chromatographic control of the identity, purity and “potency” of biomolecules used as drugs

Journal of Pharmaceutical and Biomedical Analysis [J. PHARM. BIOMED. ANAL.]. Vol. 7, no. 2. 1989, 1989, Vol.7 (2), p.185-188

1989

Volltextzugriff (PDF)

Fluorescamine Use in High-Performance Liquid Chromatographic Determination of Aminocaproic Acid in Serum

Journal of pharmaceutical sciences, 1979-02, Vol.68 (2), p.249-252

Farid, Nagy A.

1979

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Pressor responses to tyramine and norepinephrine after subchronic administration of fluoxetine to man

Life sciences (1973), 1988, Vol.42 (25), p.2569-2575

1988

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Determination of mexiletine and its metabolites in serum by liquid chromatography with fluorescence detection

Journal of chromatography, 1983-01, Vol.275 (2), p.458-462

1983

Volltextzugriff (PDF)

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

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

1983

Volltextzugriff (PDF)

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Confidence interval criteria for assessment of dose proportionality

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

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

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

Toward Energy-Efficient and Trustworthy eHealth Monitoring System

The Platelet Inhibitory Effects and Pharmacokinetics of Prasugrel After Administration of Loading and Maintenance Doses in Healthy Subjects

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

Salt form selection and characterization of LY333531 mesylate monohydrate

Switching directly to prasugrel from clopidogrel results in greater inhibition of platelet aggregation in aspirin-treated subjects

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

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

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

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

Clinical Pharmacology and Pharmacokinetics of Fluoxetine: A Review

Characterisation of natural rubber waste for pyrolysis

Thermochemical processing of rubber waste to liquid fuel

Fluoxetine: clinical pharmacology and physiologic disposition

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

Single-Dose and Steady-State Pharmacokinetics of Tomoxetine in Normal Subjects

Liquid chromatographic control of the identity, purity and “potency” of biomolecules used as drugs

Fluorescamine Use in High-Performance Liquid Chromatographic Determination of Aminocaproic Acid in Serum

Pressor responses to tyramine and norepinephrine after subchronic administration of fluoxetine to man

Determination of mexiletine and its metabolites in serum by liquid chromatography with fluorescence detection

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

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