Zobrazeno 1 - 10
of 259
pro vyhledávání: '"Jerold S. Harmatz"'
Autor:
David J. Greenblatt, Christopher D. Bruno, Jerold S. Harmatz, Qingchen Zhang, Christina R. Chow
Publikováno v:
Journal of clinical pharmacologyReferences. 62(11)
In 1979, the late Dr. Darrell R. Abernethy and colleagues began a series of clinical studies aimed at understanding the pertinent determinants of drug distribution, elimination, and clearance in obesity, and how those variables are interconnected. Th
Publikováno v:
Journal of Clinical Psychopharmacology. 40:215-219
Autor:
Jerold S. Harmatz, Su Xiang Duan, Qingchen Zhang, David J. Greenblatt, Christopher A Singleton, Zixuan Wei
Publikováno v:
The Journal of pharmacy and pharmacology. 74(1)
Objectives Acetaminophen (APAP) (paracetamol) is a widely used non-prescription drug for pain relief and antipyretic effects. The clearance of APAP is mainly through phase-2 biotransformation catalysed by UDP-glucuronosyl transferases (UGT). Dasabuvi
Autor:
Christina R. Chow, Qingchen Zhang, Jerold S. Harmatz, David J. Greenblatt, Su X. Duan, Christopher D. Bruno
Publikováno v:
British journal of clinical pharmacologyREFERENCES. 87(8)
Aims For a given passively-distributed lipophilic drug, the extent of in vivo distribution (pharmacokinetic volume of distribution, Vd ) in obese individuals increases in relation to the degree of obesity. The present study had the objective of evalu
Publikováno v:
Journal of clinical pharmacologyReferences. 61(2)
Age-related changes in disposition of diazepam and its principal active metabolite, desmethyldiazepam (DMDZ), during and after extended dosage with diazepam were studied in healthy volunteers. Eight elderly subjects (ages 61-78 years) and 7 young sub
Publikováno v:
Journal of Pharmacy and Pharmacology. 71:371-378
Objectives Resveratrol is a naturally occurring antioxidant with therapeutic potential in prevention and treatment of neoplastic disease and other human disorders. However, net clearance of resveratrol in humans is very high, mainly due to glucuronid
Publikováno v:
Journal of Clinical Psychopharmacology. 38:289-295
Purpose/background The antipsychotic agent lurasidone (Latuda®) is metabolized by Cytochrome P450-3A (CYP3A) enzymes. Coadministration with strong CYP3A inhibitors (such as ketoconazole, posaconazole, and ritonavir) is contraindicated due to the ris
Publikováno v:
Journal of Clinical Psychopharmacology. 38:1-4
Autor:
Christopher M. Rubino, Christina R. Chow, Wayne T. Nicholson, David J. Greenblatt, Jerold S. Harmatz, Maulik Patel
Publikováno v:
The Journal of Clinical Pharmacology. 58:533-540
Pharmacokinetics and antithrombotic effects of the Factor Xa inhibitor rivaroxaban were studied in subjects with mild renal insufficiency concurrently taking the P-glycoprotein and moderate CYP3A inhibitor verapamil, a drug commonly administered to p
Publikováno v:
Journal of clinical psychopharmacology. 39(3)
BACKGROUND 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 driving proficiency following bedtime doses of zolpidem. The putative explanation was