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Published in 2018 at "Clinical Pharmacology and Therapeutics"
DOI: 10.1002/cpt.1023
Abstract: Substitution by generic drugs is allowed when bioequivalence to the originator drug has been established. However, it is known that similarity in exposure may not be achieved at every occasion for all individual patients when… read more here.
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Published in 2017 at "Journal of Applied Toxicology"
DOI: 10.1002/jat.3489
Abstract: Despite the plethora of studies discussing the benefits of vitamin D on physiological functioning, few mathematical models of vitamin D predict the response of the body on low‐concentration supplementation of vitamin D under sunlight‐restricted conditions.… read more here.
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Published in 2018 at "European Journal of Clinical Pharmacology"
DOI: 10.1007/s00228-018-2444-2
Abstract: PurposeThe objective of this work was to develop a population pharmacokinetic model for a prolonged-release granule formulation of valproic acid (VPA) in children with epilepsy and to determine the doses providing a VPA trough concentration… read more here.
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Published in 2022 at "Journal of pharmacokinetics and pharmacodynamics"
DOI: 10.1007/s10928-022-09806-y
Abstract: New approaches in drug development are needed to address the growing epidemic of obesity as the prevalence of obesity increases worldwide. 2,4-Dinitrophenol (DNP) is an oxidative phosphorylation uncoupling agent that was widely used in the… read more here.
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Published in 2019 at "European Journal of Pharmaceutical Sciences"
DOI: 10.1016/j.ejps.2018.11.018
Abstract: &NA; Ezetimibe (EZE) is an extensively used antihyperlipidemic drug with an important cholesterol lowering activity. It undergoes extensive first‐pass metabolism to form its active glucuronide metabolite (EZEG). Both drugs exhibit complex pharmacokinetic profiles attributed mainly… read more here.
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Published in 2019 at "Veterinary anaesthesia and analgesia"
DOI: 10.1016/j.vaa.2019.04.009
Abstract: OBJECTIVE To develop a population pharmacokinetic model for propofol target-controlled infusion (TCI) in dogs and to evaluate its performance for use in the clinical setting. STUDY DESIGN Prospective clinical study. ANIMALS A group of 40… read more here.
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Published in 2018 at "Regulatory Toxicology and Pharmacology"
DOI: 10.1016/j.yrtph.2018.01.029
Abstract: ABSTRACT Phosphatidylethanol (PEth) is increasingly used as a biomarker of heavy drinking. Many different forms of PEth can form in red blood cell membranes from the action of the enzyme phospholipase D. PEth has a… read more here.
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Published in 2018 at "Anaesthesia"
DOI: 10.1111/anae.14002
Abstract: United States of America 2008; 105: 1309–14. 2. Pandit JJ. Monitoring (un)consciousness: the implications of a new definition of ‘anaesthesia’. Anaesthesia 2014; 69: 801–7. 3. Sep ulveda V PO, Carrasco E, Tapia LF, et al.… read more here.
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Published in 2019 at "British Journal of Clinical Pharmacology"
DOI: 10.1111/bcp.13902
Abstract: Agomelatine is an antidepressant for major depressive disorders. It undergoes extensive first‐pass hepatic metabolism and displays irregular absorption profiles and large interindividual variability (IIV) and interoccasion variability of pharmacokinetics. The objective of this study was… read more here.
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Published in 2020 at "British Journal of Clinical Pharmacology"
DOI: 10.1111/bcp.14278
Abstract: Escitalopram (SCIT) is frequently prescribed to breastfeeding women. Available information on SCIT excretion into breast milk is based on heterogeneous and incomplete data. A population pharmacokinetic model that aimed to better characterize maternal and infant… read more here.
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Published in 2021 at "British journal of clinical pharmacology"
DOI: 10.1111/bcp.14883
Abstract: AIMS There are several limitations to the existing method of administering cefoxitin as a prophylactic antibiotic, and the limitations may be overcome by applying the target-concentration controlled infusion (TCI) method. Population pharmacokinetic parameters are required… read more here.