Comparison of preference for rizatriptan 10-mg wafer versus sumatriptan 50-mg tablet in migraine

被引:34
作者
Pascual, J
Bussone, G
Hernandez, JF
Allen, C [1 ]
Vrijens, F
Patel, K
机构
[1] Merck & Co Inc, Dept WS3C90, 1 Merck Dr, Whitehouse Stn, NJ 08889 USA
[2] Hosp Marques de Valdecilla, Santander, Spain
[3] Ist Neurol, Milan, Italy
[4] Hosp Mil Cent, Bogota, Colombia
[5] Merck Sharp & Dohme Europe Inc, Brussels, Belgium
关键词
rizatriptan; sumatriptan; preference; migraine;
D O I
10.1159/000052143
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Rizatriptan (MAXALT(TM), a registered trademark of Merck & Co. Inc.) is a selective 5-HT1B/1D receptor agonist with rapid oral absorption and early onset of action in the acute treatment of migraine. This randomized, open-label, crossover outpatient study assessed the preference of 481 patients for rizatriptan 10-mg rapidly disintegrating tablets versus sumatriptan (IMIGRAN(TM), a registered trademark of GlaxoWellcome PLC) 50-mg tablets in the treatment of a single migraine attack with each thera-py. Almost twice as many patients preferred rizatriptan 10-mg rapidly disintegrating tablet to sumatriptan 50-mg tablet (64.3 vs. 35.7%, p less than or equal to 0.001). Faster relief of headache pain was the most important reason for the preference, cited by 46.9% of patients preferring rizatriptan and 43.4% of patients who preferred sumatriptan. Headache relief at 2 h was 75.9% with rizatriptan and 66.6% with sumatriptan (p less than or equal to 0.001), with rizatriptan being superior to sumatriptan within 30 min of dosing. Fifty-five percent of patients were pain free 2 h after rizatriptan, com pa red with 42.1% treated with sumatriptan (p less than or equal to 0.001), rizatriptan being superior with in 1 h of treatment. Forty-one percent of patients taking rizatriptan were pain free at 2 h and had no recurrence or need for additional medication, compared to 32.3% of patients on sumatriptan. Rizatriptan was also superior to sumatriptan in terms of the proportions of patients with no nausea, phonophobia or photophobia, and patients with normal function 2 h after treatment intake (p < 0.05). More patients were (completely, very or somewhat) satisfied 2 h after treatment with rizatriptan (73.3%) than 2 h after treatment with sumatriptan (59.0%) (p <= 0.001). Additionally, 2 h after the dose, more patients found rizatriptan to be very convenient, convenient or somewhat convenient (87.2%) than they did sumatriptan (76.3%) (p less than or equal to 0.001). Both active treatments were well tolerated. The most common side effects with rizatriptan and sumatriptan were nausea (6.6 and 6.9% of patients, respectively), dizziness (6.1 and 5.8%) and somnolence (7.4 and 6.7%). Copyright (C) 2001 S. Karger AG, Basel.
引用
收藏
页码:275 / 283
页数:9
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