Fowler L K
J Int Med Res. 1979;7(5):379-82. doi: 10.1177/030006057900700508.
An interim report at six months of a post-marketing surveillance study of Euhypnos Forte, a new high-dose temazepam preparation for the treatment of insomniac patients resistant to conventional hypnotic dosage. The analysis includes 2,043 First Reports (FRs) of two weeks treatment and 669 Second Reports (SRs) of three months treatment. More than 95% of the patients took a nightly dose of two capsules, temazepam 40 mg. Adverse reactions were generally acceptable, consisting mainly of headache, vivid dreams, gastro-intestinal disturbances and hangover effects. The preparation was effective in 88.6% of patients at two weeks and 95.8% at three months. All patients had previously found other hypnotics ineffective. Euhypnos Forte was rated effective by 85.5% of the 874 patients who had previously found nitrazepam unsatisfactory, and by 90.0% of the 201 who found barbiturates unsatisfactory.
一项关于新型高剂量替马西泮制剂Euhypnos Forte的上市后监测研究的六个月中期报告,该制剂用于治疗对常规催眠剂量有抗性的失眠患者。分析包括2043份两周治疗的首次报告(FRs)和669份三个月治疗的二次报告(SRs)。超过95%的患者每晚服用两粒胶囊,即40毫克替马西泮。不良反应总体上可以接受,主要包括头痛、生动梦境、胃肠道不适和宿醉效应。该制剂在两周时对88.6%的患者有效,三个月时对95.8%的患者有效。所有患者此前都发现其他催眠药无效。在874名此前认为硝西泮不满意的患者中,85.5%的患者认为Euhypnos Forte有效;在201名认为巴比妥类药物不满意的患者中,90.0%的患者认为该制剂有效。