Generic atypical antipsychotic drugs in Belgium: their influence and implications

Author:

Godman Brian123,De Bruyn Kristien4,Miranda Jamilette5,Raschi Emanuel6,Bennie Marion27,Barbui Corrado8,Simoens Steven9

Affiliation:

1. Department of Laboratory Medicine, Division of Clinical Pharmacology, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden.

2. Strathclyde Institute of Pharmacy & Biomedical Sciences, University of Strathclyde, Glasgow, UK

3. National Institute of Science & Technology on Innovation on Neglected Diseases, Centre for Technological Development in Health, Oswaldo Cruz Foundation (Fiocruz), Rio de Janeiro, Brazil

4. Statistics Department, Association of Belgian Pharmacists, Archimedesstraat 11, B-1000 Brussels, Belgium

5. Department of Development, Public Healthcare Services Committee Administration, Stockholm County Council, Stockholm, Sweden

6. Department of Medical & Surgical Sciences, Alma Mater Studiorum – University of Bologna, Bologna, Italy

7. Public Health & Intelligence Strategic Business Unit, NHS National Services Scotland, Edinburgh, EH12 9EB, UK

8. WHO Collaborating Centre for Research and Training in Mental Health & Service Evaluation, Department of Public Health & Community Medicine, Section of Psychiatry, University of Verona, Policlinico G.B. Rossi, Piazzale L.A. Scuro 10, 37134 Verona, Italy

9. KU Leuven, Department of Pharmaceutical & Pharmacological Sciences, KU Leuven, Herestraat 49, O & N 2 Bus 521, 3000 Leuven, Belgium

Abstract

Introduction: Generic atypical antipsychotic drugs should be a focus of attention given their expenditure. However, there is a recognized need to tailor treatments. There were no specific measures in Belgium to enhance the prescribing of oral risperidone following generics in January 2008. Prescribing restrictions have remained for long-acting risperidone injections throughout. Objective: Assess changes in risperidone utilization before and after oral generics were reimbursed, as well as the utilization and expenditure of the various risperidone preparations. Method: Principally a retrospective observational study and interrupted time series design. Results: As expected, no increased utilization of oral risperidone after generics. Both originator and generic oral risperidone prescribed, with the originator reducing its price. Generic risperidone was 59% below prepatent loss prices by September 2012. Conclusion: Authorities cannot rely on a ‘spill over’ of learning from other disease areas to affect changes in physician prescribing habits. Specific measures are needed to encourage generic risperidone where appropriate. However, their influence will be limited by the complexity of the disease area.

Publisher

Future Medicine Ltd

Subject

Health Policy

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