Free Content Concurrent administration of donepezil HCl and risperidone in patients with schizophrenia: assessment of pharmacokinetic changes and safety following multiple oral doses

Authors: Reyes, Josephine F.; Preskorn, Sheldon H.1; Khan, Ahsan1; Kumar, Dinesh2; Cullen, Edward I.; Perdomo, Carlos A.2; Pratt, Raymond D.

Source: British Journal of Clinical Pharmacology, Volume 58, Supplement 1, November 2004 , pp. 50-57(8)

Publisher: Wiley-Blackwell

Buy & download fulltext article:

You have access to the full text article on a website external to ingentaconnect.

Please click here to view this article on Wiley Online Library.

You may be required to register and activate access on Wiley Online Library before you can obtain the full text. If you have any queries please visit Wiley Online Library

Abstract:

Aim

This open-label, multiple-dose trial investigated the effect of concurrent administration of donepezil HCl with risperidone on the pharmacokinetics (PK) and safety profiles of both drugs. Methods

Sixteen male patients with schizophrenia, who were receiving stable, physician-optimized risperidone (1-4 mg twice daily), and 15 healthy age- and weight-matched male controls, received donepezil HCl 5 mg daily for 7 days. Patients with schizophrenia remained on their physician-optimized dose of risperidone throughout the study. Pharmacokinetic parameters (Cmax, tmax and AUC) were assessed from plasma drug concentrations measured in blood collected before, during and after administration (for 12 h after risperidone on days 0 and 7, and for 24 h after donepezil HCl on day 7). Results

The mean age of all the subjects was 38.5 years. Donepezil PK parameters were similar between patients taking donepezil HCl + risperidone (AUC0−24 h = 329.0 ± 17.2 ng·h ml−1) and controls taking donepezil HCl alone (AUC0−24 h = 354.7 ± 28.2 ng·h ml−1). Pharmacokinetic parameters for risperidone and 9-OH risperidone were not altered in patients with schizophrenia after 7 days of donepezil HCl administration (AUC0−12 h standardized by dose: risperidone = 59.6 ± 16.3 ng·h ml−1 at day 0, 56.0 ± 15.8 ng·h ml−1 at day 7; 9-OH risperidone = 162.1 ± 19.2 ng·h ml−1 at day 0, 163.3 ± 15.0 ng·h ml−1 at day 7). The most common adverse event in both treatment groups was diarrhoea (6/16 risperidone + donepezil HCl patients and 9/16 donepezil HCl only subjects). There were no significant changes in physical examination, ECG, vital signs or treatment-emergent abnormal laboratory values associated with either of the treatment regimens. No subject developed extrapyramidal side-effects following donepezil administration. Conclusions

These results suggest that once-daily dosing of 5 mg donepezil HCl does not alter the PK of risperidone in patients with schizophrenia. The combination of risperidone and donepezil HCl was well tolerated.

Keywords: acetylcholinesterase inhibitor; donepezil hydrochloride; PK interaction; risperidone; schizophrenia

Document Type: Research article

DOI: http://dx.doi.org/10.1111/j.1365-2125.2004.01817.x

Affiliations: 1: Psychiatric Research Institute, Wichita, KS, USA 2: Biometrics Biostatistics, and

Publication date: 2004-11-01

Related content

Tools

Key

Free Content
Free content
New Content
New content
Open Access Content
Open access content
Subscribed Content
Subscribed content
Free Trial Content
Free trial content

Text size:

A | A | A | A
Share this item with others: These icons link to social bookmarking sites where readers can share and discover new web pages. print icon Print this page