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PJ Online homeThe Pharmaceutical Journal
Vol 276 No 7392 p308
18 March 2006

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Scottish Medicines Consortium offers more advice for NHS Scotland

Lumiracoxib (Prexige), a selective cyclo-oxygenase 2 (COX-2) inhibitor, is one of four products that have been approved by the Scottish Medicines Consortium for use within NHS Scotland.

Lumiracoxib is accepted for the symptomatic relief of osteoarthritis for patients in whom a COX-2 inhibitor is deemed appropriate —but not for patients with established ischaemic heart disease, cerebrovascular disease, peripheral arterial disease or moderate or severe congestive heart failure. It should be used cautiously in patients at significant cardiovascular risk.

Growth hormone injection somatroprin (Genotropin) is accepted for restricted use in the treatment of growth delay in children born small for gestational age and who fail to show catch-up growth by at least four years of age.

The new sildenafil formulation, Revatio, has been accepted for the treatment of pulmonary arterial hypertension, to improve exercise capacity in patients with the condition. This is an orphan indication with limited evidence from short-term clinical trials, and is therefore restricted to initiation by experts in the management of pulmonary vascular disease and specialists working in the Scottish Peripheral Vascular Unit, at the Western Infirmary, Glasgow.

The SMC has also approved budesonide in the new Easyhaler inhalation device. Available in three strengths, the inhaled corticosteroid is accepted for the treatment of mild, moderate or severe persistent asthma in adults and children over six years of age.

The following medicines were rejected by the SMC: aprepitant (Emend) for prevention of nausea and vomiting associated with moderately emetogenic cancer chemotherapy; modafinil (Provigil) for treatment of excessive sleepiness associated with obstructive sleep apnoea/hypopnoea syndrome; rasagiline (Azilect) for treatment of idiopathic Parkinson’s disease as adjunct therapy (with levodopa) in patients with end-of-dose fluctuations, or as monotherapy (without levodopa); and temozolomide (Temodal) for treatment of newly diagnosed glioblastoma multiforme concomitantly with radiotherapy and subsequently as monotherapy.

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