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Nonlinear Pharmacokinetics: Dependence of Elimination Half-Life and Dose Clearance01:23

Nonlinear Pharmacokinetics: Dependence of Elimination Half-Life and Dose Clearance

The elimination half-life and drug clearance of drugs following nonlinear kinetics can vary with dosage. The Michaelis-Menten parameters and drug concentration influence these factors. As the dose increases, the elimination half-life tends to lengthen, resulting in a reduction in clearance and a disproportionately larger area under the curve. The total clearance can be derived from the Michaelis-Menten equation for drugs following a one-compartment model.
A study on guinea pigs examined the...
Rational Dosage Regimen: Maintenance Dose and Loading Dose01:24

Rational Dosage Regimen: Maintenance Dose and Loading Dose

A rational dosage regimen considers a drug's pharmacokinetics, including its absorption, distribution, metabolism, and elimination from the body. By understanding these factors, the appropriate dosage can be determined, and the dosing schedule can be designed to achieve and maintain the desired therapeutic effect while minimizing adverse effects.
In most cases, drugs are administered repetitively or infused continuously to maintain a steady-state concentration in the body. At a steady state,...
Determination of Multiple Dosing Parameters: Loading and Maintenance Doses01:25

Determination of Multiple Dosing Parameters: Loading and Maintenance Doses

A loading dose is an essential pharmacological strategy to rapidly achieve the target plasma drug concentration necessary for an immediate therapeutic effect. This approach is especially critical for drugs characterized by slow absorption or extended half-lives, where delaying therapeutic plasma levels could compromise treatment outcomes. By administering a loading dose, clinicians ensure a prompt onset of drug action, even for agents with complex pharmacokinetic profiles.Achieving steady-state...
Drug Accumulation During Multiple Dosing: Intermittent IV Infusions01:24

Drug Accumulation During Multiple Dosing: Intermittent IV Infusions

Intermittent intravenous (IV) infusion is a method of drug administration where medications are delivered over short infusion periods followed by intervals of no drug delivery. This approach helps to prevent sustained high drug concentrations in the bloodstream, reducing the risk of adverse effects associated with prolonged exposure. Unlike continuous infusion, steady-state concentrations may not be achieved during a single dosing cycle but can be reached through repeated...
IV Infusion to Oral Dosing: Conversion Methods01:28

IV Infusion to Oral Dosing: Conversion Methods

The development of extended-release formulations has facilitated the transition from intravenous to oral medication, offering a more convenient and patient-friendly approach to drug administration. This transition, however, requires careful management to ensure that therapeutic drug levels are maintained, preserving efficacy and avoiding adverse effects. Understanding pharmacokinetic principles and dosage calculations is critical during this process.Pharmacokinetics of the...
Oral Drug Delivery Systems: Continuous-Release Systems01:26

Oral Drug Delivery Systems: Continuous-Release Systems

Continuous-release drug delivery systems offer a strategic approach to maintaining therapeutic drug levels over extended periods following oral administration. By modulating the release rate of active pharmaceutical ingredients, these systems minimize fluctuations in plasma concentrations, which enhances clinical efficacy and reduces the need for frequent dosing. Such characteristics make them particularly advantageous in managing chronic diseases where patient adherence and stable drug...

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Updated: Jun 8, 2026

Methods to Quantify Pharmacologically Induced Alterations in Motor Function in Human Incomplete SCI
14:55

Methods to Quantify Pharmacologically Induced Alterations in Motor Function in Human Incomplete SCI

Published on: April 18, 2011

High-dose loading with extended release quetiapine.

B-J Chae1

  • 1Department of Psychiatry, Daedong Hospital, Dalseo-gu, Daegu, Korea. bjchae@korea.com

Journal of Clinical Pharmacy and Therapeutics
|September 14, 2010
PubMed
Summary
This summary is machine-generated.

Maximum dose extended release quetiapine fumarate (quetiapine XR) loading was generally well tolerated in schizophrenia patients. However, one patient with a history of cerebral infarction experienced serious side effects.

Related Experiment Videos

Last Updated: Jun 8, 2026

Methods to Quantify Pharmacologically Induced Alterations in Motor Function in Human Incomplete SCI
14:55

Methods to Quantify Pharmacologically Induced Alterations in Motor Function in Human Incomplete SCI

Published on: April 18, 2011

Area of Science:

  • Psychiatry
  • Pharmacology
  • Clinical Therapeutics

Background:

  • Schizophrenia treatment often involves extended-release formulations for improved adherence and sustained drug levels.
  • Extended release quetiapine fumarate (quetiapine XR) is a widely used atypical antipsychotic for managing schizophrenia.
  • Determining optimal dosing strategies, including initial loading doses, is crucial for efficacy and tolerability.

Observation:

  • A case series involving five schizophrenia patients initiated on the maximum dose of 800 mg quetiapine XR was observed.
  • Four out of five patients tolerated the maximum dose loading well.
  • One patient with a history of cerebral infarction experienced significant adverse events, including bladder distention and dizziness.

Findings:

  • Initial loading with the maximum dose of 800 mg quetiapine XR appears to be generally well-tolerated in the majority of schizophrenia patients.
  • The presence of concurrent conditions, such as a history of cerebral infarction, may increase the risk of serious side effects with high-dose quetiapine XR loading.

Implications:

  • Maximum dose loading of quetiapine XR may be a safe and tolerable strategy for most schizophrenia patients without significant comorbidities.
  • Caution and careful patient selection are advised when initiating high-dose quetiapine XR in patients with a history of cerebrovascular events.
  • Further research is warranted to elucidate the specific risks associated with high-dose quetiapine XR loading in vulnerable patient populations.