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Safety and tolerability of once-daily extended release quetiapine fumarate in acute schizophrenia: pooled data from randomised, double-blind, placebo-controlled studies

✍ Scribed by Didier Meulien; Karin Huizar; Martin Brecher


Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
130 KB
Volume
25
Category
Article
ISSN
0885-6222

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✦ Synopsis


Abstract

Introduction

Extended release quetiapine fumarate (quetiapine XR) is a new formulation that allows once‐daily dosing and a titration regimen that is simpler than that of immediate release quetiapine (quetiapine IR) and may potentially increase patients' adherence to their prescribed medication.

Methods

The tolerability of quetiapine XR was examined in an analysis of pooled data from three Phase III, double‐blind, placebo‐controlled, randomised studies with quetiapine IR as a reference treatment.

Results

The overall incidence of adverse events (AEs) was similar for quetiapine XR (69.5%) and quetiapine IR (72.5%). Most AEs were mild to moderate in severity and in line with those observed with quetiapine IR. The more rapid dose titration of quetiapine XR did not produce any new safety concerns and was as well tolerated as the regimen for quetiapine IR.

Conclusions

The results of this pooled analysis show that quetiapine XR administered once daily is generally as well tolerated as quetiapine IR given twice daily. These data, together with the simpler dose‐titration of quetiapine XR that allowed therapeutically effective doses to be reached by Day 2, suggest that this formulation potentially may improve adherence in patients with schizophrenia. Copyright © 2010 John Wiley & Sons, Ltd.


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Efficacy and tolerability of extended re
✍ Dan J. Stein; Borwin Bandelow; Charles Merideth; Bengt Olausson; Johan Szamosi; 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 377 KB 👁 2 views

## Objective Prospectively planned pooled analysis evaluating efficacy and tolerability of acute quetiapine XR monotherapy in generalised anxiety disorder. ## Methods Data from three 10‐week, randomised, double‐blind, placebo‐controlled studies of similar design were analysed. ## Results At Wee