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BMJ 2003;326:1212 (31 May), doi:10.1136/bmj.326.7400.1212
| The first 150 words of the full text of this article appear below. |
EDITORSudlow and Counsell think that the UK government's risk sharing scheme for the provision of disease modifying drugs for multiple sclerosis (interferon beta and glatiramer acetate) may be flawed.1
Firstly, the risk sharing scheme was introduced to ensure that the disease modifying drugs in question are acquired by the NHS in a cost effective manner, which will be reviewed by the Department of Health at scheduled time points, with the required adjustments being made to ensure the agreed cost effectiveness threshold is maintained.
Secondly, pivotal, randomised, placebo controlled studies lasting for up to five years already show that these drugs are effective and well tolerated. The longer term outcome is less certain, although evidence both from observational studies and more than 15 years of clinical practice in the United States indicates that efficacy continues and there have been no unexpected safety issues.
We agree that additional robust long
Jacqueline C Napier, associate medical director
Schering Health Care, Burgess Hill, West Sussex RH15 9NE jnapier@schering.co.uk
Richard Francis, country manager United Kingdom and Ireland
Biogen, Maidenhead, Berkshire SL6 3UD
Glyn Wright, general manager
Teva Pharmaceuticals, High Wycombe, Buckinghamshire HP13 7SS