Search Results - "Harmatz, Jerold S."
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Gender differences in pharmacokinetics and pharmacodynamics of zolpidem following sublingual administration
Published in Journal of clinical pharmacology (01-03-2014)“…The effect of dose and gender on the pharmacokinetics (PK) and pharmacodynamics (PD) of zolpidem after administration of a buffered zolpidem sublingual tablet…”
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Effect of a herbal extract containing curcumin and piperine on midazolam, flurbiprofen and paracetamol (acetaminophen) pharmacokinetics in healthy volunteers
Published in British journal of clinical pharmacology (01-02-2013)“…Aims Turmeric extract derived curcuminoids (curcumin, demethoxycurcumin and bisdemethoxycurcumin) are currently being evaluated for the treatment of cancer and…”
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3
Mechanism of cytochrome P450-3A inhibition by ketoconazole
Published in Journal of pharmacy and pharmacology (01-02-2011)“…Objectives Ketoconazole is extensively used as an index inhibitor of cytochrome P450‐3A (CYP3A) activity in vitro and in vivo, but the mechanism of…”
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4
Favipiravir inhibits acetaminophen sulfate formation but minimally affects systemic pharmacokinetics of acetaminophen
Published in British journal of clinical pharmacology (01-11-2015)“…Aims The antiviral agent favipiravir is likely to be co‐prescribed with acetaminophen (paracetamol). The present study evaluated the possiblility of a…”
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Comparison of Pharmacokinetic Profiles of Zolpidem Buffered Sublingual Tablet and Zolpidem Oral Immediate-Release Tablet: Results from a Single-Center, Single-Dose, Randomized, Open-Label Crossover Study in Healthy Adults
Published in Clinical therapeutics (01-05-2013)“…Abstract Background A zolpidem sublingual tablet (ZST) formulation was recently approved by the US Food and Drug Administration to treat middle-of-the-night…”
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Evidence for oxazepam as an in vivo probe of UGT2B15: oxazepam clearance is reduced by UGT2B15 D85Y polymorphism but unaffected by UGT2B17 deletion
Published in British journal of clinical pharmacology (01-11-2009)“…WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT • UDP‐glucuronosyltransferase (UGT) 2B15 is a major drug glucuronidation enzyme expressed in human liver. • Oxazepam…”
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Serum concentrations and clinical effects of atorvastatin in patients taking grapefruit juice daily
Published in British journal of clinical pharmacology (01-09-2011)“…WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT • In previous studies of healthy volunteers, administration of atorvastatin with very large quantities of grapefruit…”
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Zolpidem and Gender: Are Women Really At Risk?
Published in Journal of clinical psychopharmacology (01-05-2019)“…In 2013 the Food and Drug Administration (FDA) claimed the existence of new data showing women to be at risk for excessive daytime sedation and impaired…”
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Ritonavir is the best alternative to ketoconazole as an index inhibitor of cytochrome P450‐3A in drug–drug interaction studies
Published in British journal of clinical pharmacology (01-09-2015)“…Aims The regulatory prohibition of ketoconazole as a CYP3A index inhibitor in drug–drug interaction (DDI) studies has compelled consideration of alternative…”
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Inhibition of human cytochromes P450 by components of Ginkgo biloba
Published in Journal of pharmacy and pharmacology (01-08-2004)“…The extraction, isolation and characterization of 29 natural products contained in Ginkgo biloba have been described, which we have now tested for their…”
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Effect of lipophilicity on drug distribution and elimination: Influence of obesity
Published in British journal of clinical pharmacology (01-08-2021)“…Aims For a given passively‐distributed lipophilic drug, the extent of in vivo distribution (pharmacokinetic volume of distribution, Vd) in obese individuals…”
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12
Drug Disposition in Subjects With Obesity: The Research Work of Darrell R. Abernethy
Published in Journal of clinical pharmacology (01-11-2022)“…In 1979, the late Dr. Darrell R. Abernethy and colleagues began a series of clinical studies aimed at understanding the pertinent determinants of drug…”
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Comparison between Cytochrome P450 (CYP) Content and Relative Activity Approaches to Scaling from cDNA-Expressed CYPs to Human Liver Microsomes: Ratios of Accessory Proteins as Sources of Discrepancies between the Approaches
Published in Drug metabolism and disposition (01-12-2000)“…Relative activity factors (RAFs) and immunoquantified levels of cytochrome P450 (CYP) isoforms both have been proposed as scaling factors for the prediction of…”
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Clinical Consequences of Altered Drug Disposition in Obesity: Call for Change
Published in Journal of clinical pharmacology (01-11-2023)“…Abstract Obesity is a serious condition with many known comorbid conditions and other health risks. Despite the rising global rates of obesity, drug…”
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Update on Psychotropic Drug Prescribing in the United States: 2014-2015
Published in Journal of clinical psychopharmacology (01-02-2018)Get full text
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Race, Gender, and Genetic Polymorphism Contribute to Variability in Acetaminophen Pharmacokinetics, Metabolism, and Protein-Adduct Concentrations in Healthy African-American and European-American Volunteers
Published in The Journal of pharmacology and experimental therapeutics (01-09-2017)“…Over 30 years ago, black Africans from Kenya and Ghana were shown to metabolize acetaminophen faster by glucuronidation and slower by oxidation compared with…”
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Pharmacokinetic properties of zolpidem in elderly and young adults: possible modulation by testosterone in men
Published in British journal of clinical pharmacology (01-09-2003)“…Aims The influence of ageing on the pharmacokinetics of zolpidem, an extensively prescribed hypnotic medication, was evaluated in healthy human volunteers…”
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Diazepam in the Elderly: Looking Back, Ahead, and at the Evidence
Published in Journal of clinical psychopharmacology (01-05-2020)Get full text
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Vortioxetine Disposition in Obesity: Potential Implications for Patient Safety
Published in Journal of clinical psychopharmacology (01-06-2018)“…Obesity and depression are common comorbid conditions. The objective of the study was to evaluate the effect of obesity on the pharmacokinetics of the…”
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Fluvoxamine impairs single‐dose caffeine clearance without altering caffeine pharmacodynamics
Published in British journal of clinical pharmacology (01-11-2005)“…Background Coadministration of fluvoxamine impairs the clearance of caffeine and prolongs its elimination half‐life, which is attributable to inhibition of…”
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