首页> 外国专利> MEDICINAL BASIS ON LEVOMILNACIPRAN, INTENDED FOR FUNCTIONAL REHABILITATION AFTER ACUTE NEUROLOGICAL DISORDERS

MEDICINAL BASIS ON LEVOMILNACIPRAN, INTENDED FOR FUNCTIONAL REHABILITATION AFTER ACUTE NEUROLOGICAL DISORDERS

机译:左旋丙氨西环的药用基础,旨在用于急性神经系统疾病后的功能康复

摘要

1. A mixture of levomylnacipran and dextromylnacipran containing dextromylnacipran in a concentration not exceeding 5 wt.% Of this mixture, used as a medicine for recovery and functional rehabilitation after an acute neurological disorder and its relapses. 2. The mixture according to claim 1, used for patients who are diagnosed with acute cerebrovascular accident of ischemic or hemorrhagic origin. The mixture according to claim 1, used for patients who are diagnosed with traumatic brain damage. A pharmaceutical composition containing at least one pharmaceutically acceptable excipient and a mixture of levomylnacipran and dextromylnacipran containing dextromylnacipran in a concentration not exceeding 5 wt.% Of this mixture as an active ingredient, used as a medicine for recovery and functional rehabilitation after an acute neurological disorder and its relapses. 5. The pharmaceutical composition according to claim 4, used for patients who are diagnosed with acute cerebrovascular accident. The pharmaceutical composition according to claim 4, used for patients diagnosed with traumatic brain damage. A pharmaceutical composition according to any one of claims 4 to 6, characterized in that the daily dose of levomylnacipran is from 50 to 200 mg. The pharmaceutical composition according to any one of claims 4 to 6, characterized in that said composition is in a form having a modified absorption in the intestine, which makes it possible to administer one dose per day.
机译:1.一种左旋炔诺普生和右旋葡糖基萘普生的混合物,其中含有右旋葡糖基萘普生的浓度不超过该混合物的5重量%,用作在急性神经系统疾病和其复发后恢复和功能康复的药物。 2.根据权利要求1的混合物,用于诊断为缺血性或出血性源性急性脑血管意外的患者。 2.根据权利要求1所述的混合物,用于诊断为脑外伤的患者。包含至少一种药学上可接受的赋形剂以及含有浓度不超过该混合物的5wt。%的糊精基萘普生的左旋吗啡普林和右旋糊精的混合物的药物组合物,用作急性神经系统疾病后恢复和功能康复的药物及其复发。 5.根据权利要求4的药物组合物,用于诊断为急性脑血管意外的患者。 5.根据权利要求4所述的药物组合物,用于诊断为脑外伤的患者。 7.根据权利要求4至6中任一项所述的药物组合物,其特征在于,左旋柳氮普康的日剂量为50至200mg。 7.根据权利要求4至6中任一项所述的药物组合物,其特征在于,所述组合物为在肠中具有改善的吸收的形式,这使得每天可以给药一剂。

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