Literature DB >> 15560318

Acceptability and disintegration rates of orally disintegrating risperidone tablets in patients with schizophrenia or schizoaffective disorder.

Pierre Chue1, Ron Welch, Carin Binder.   

Abstract

OBJECTIVE: To investigate the disintegration profile, acceptability, and tolerability of orally disintegrating risperidone tablets in patients with schizophrenia or schizoaffective disorder.
METHOD: Ten patients stable for at least 10 days on monotherapy with oral risperidone 2 mg to 4 mg taken once daily were switched for 7 days to an equivalent dosage of orally disintegrating risperidone. Visual assessments for time to initial and complete disintegration were collected at each visit. Clinical Global Impression of Severity scores were collected at baseline and at the last visit. Patient acceptance of the new formulation, rated according to a visual analog scale, was obtained at the last visit.
RESULTS: All patients maintained stable clinical status. Mean time to initial disintegration was 5.1 seconds, SD 0.8, and mean time to complete disintegration was 29.4 seconds, SD 18.4. The formulation was rated as very acceptable. Adverse events were reported by 5 patients; all were mild.
CONCLUSION: The orally disintegrating risperidone tablets were well tolerated and rated as very acceptable by all patients.

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Year:  2004        PMID: 15560318     DOI: 10.1177/070674370404901009

Source DB:  PubMed          Journal:  Can J Psychiatry        ISSN: 0706-7437            Impact factor:   4.356


  3 in total

1.  Development and evaluation of artemether taste masked rapid disintegrating tablets with improved dissolution using solid dispersion technique.

Authors:  Punit P Shah; Rajashree C Mashru
Journal:  AAPS PharmSciTech       Date:  2008-03-20       Impact factor: 3.246

2.  Taste masking of ondansetron hydrochloride by polymer carrier system and formulation of rapid-disintegrating tablets.

Authors:  Shagufta Khan; Prashant Kataria; Premchand Nakhat; Pramod Yeole
Journal:  AAPS PharmSciTech       Date:  2007-06-22       Impact factor: 3.246

3.  An in vitro analysis of disintegration times of different formulations of olanzapine orodispersible tablet: a preliminary report.

Authors:  David Hobbs; Jamie Karagianis; Tamas Treuer; Joel Raskin
Journal:  Drugs R D       Date:  2013-12
  3 in total

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