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  药店国别: 日本药房
产地国家: 日本
所属类别: 神经系统药物->抗抑郁药
处方药:处方药
包装规格: 50毫克/颗粒 10克/瓶
计价单位:
   
生产厂家中文参考译名:
阿斯利康
生产厂家英文名:
AstraZeneca
该药品相关信息网址1:
http://www.igenericdrugs.com/gd.cgi?notran=1&s=Quetiapine&search=SEARCH
原产地英文商品名:
Quetiapine oral granule 50mg 100g/bottle
原产地英文药品名:
Quetiapine
中文参考商品译名:
奎硫平 50毫克/颗粒 10克/瓶
原产地国家批准上市年份:
0000/00/00
英文适应病症1:
schizophrenia
英文适应病症2:
depressive disorder
临床试验期:
完成
中文适应病症参考翻译1:
精神分裂症
中文适应病症参考翻译2:
郁药
药品信息:
Quetiapine奎硫平是一种抗精神病药物药。它通过改变大脑中的化学物质的行为。 喹硫平用于治疗精神分裂症的成人和儿童谁是至少13岁。  喹硫平用于治疗双相情感障碍(躁狂抑郁症)的成人和儿童谁是至少10岁。 喹硫平也一起使用抗抑郁药物来治疗成人重度抑郁症。 缓释喹硫平(思瑞康XR )只能用于成人,不应该给任何人未满18岁。 喹硫平也可用于这种药物指南中未列出的目的。 奎硫平是一种抗精神病药物(抗精神病药)的药物。该药物表现出对血清素5HT2受体与多巴胺D1和D2受体在脑相比具有高亲和力。也有喹硫平对组胺和α1-受体具有高亲和力和不太明显 - 在α2-受体。 这种药物具有的m胆碱能受体和苯二氮卓受体无亲和力。喹硫平的剂量有效阻断多巴胺D2受体只引起微弱僵住。喹硫平选择性降低脑边缘多巴胺神经元的A10-相比与参与运动功能A9- nigrostriatalnymi神经元的活性。此药不会引起长期提高催乳素水平。  按照喹硫平的正电子发射断层作用于血清素5HT2和多巴胺D2受体的结果可以延长至12小时。 喹硫平是属于苯并异恶唑衍生物的化学类精神治疗药物,并表示对精神分裂症的治疗。奎硫平是一种选择性单胺拮抗剂与五羟色胺2型( 5HT ,多巴胺D1和D2 ,组胺H1高亲和力和肾上腺素能α- 1和α 2受体。喹硫平具有胆碱能毒蕈碱或苯二氮卓受体,倦睡和体位性低血压无显著亲和力与使用奎硫平的关联机构可能会由组胺H1和肾上腺素能α- 1受体,肾上腺素能分别为A1受体。喹硫平\的拮抗作用,其拮抗作用来解释或许可以解释用此药观察到的体位性低血压。 喹硫平用于治疗精神分裂症和双相情感障碍(躁狂抑郁症) 。它有助于缓解精神分裂症和双相情感障碍的常见症状,如扭曲的思维和情绪不稳定。喹硫平也一起使用其他药物来治疗抑郁症。 Quetiapine - Quetiapine is an antipsychotic medicine. It works by changing the actions of chemicals in the brain. Quetiapine is used to treat schizophrenia in adults and children who are at least 13 years old. Quetiapine is used to treat bipolar disorder (manic depression) in adults and children who are at least 10 years old. Quetiapine is also used together with antidepressant medications to treat major depressive disorder in adults. Extended-release Quetiapine (Seroquel XR) is for use only in adults and should not be given to anyone younger than 18 years old. Quetiapine may also be used for purposes not listed in this medication guide. Quetiapine is an antipsychotic (neuroleptic) drug. This medication exhibits a high affinity for serotonin 5HT2-receptors compared with dopamine D1- and D2-receptors in the brain. Also Quetiapine has a high affinity for histamine and alpha1-receptors and a less pronounced - to the alpha2-receptors. This drug has no affinity for the m-cholinergic receptors and benzodiazepine receptors. Quetiapine in the dose effectively blocking dopamine D2-receptors causing only weak catalepsy. Quetiapine selectively reduces the activity of mesolimbic dopamine neurons in A10-compared with A9-nigrostriatalnymi neurons involved in motor function. This medicine does not cause long raise prolactin levels. In accordance with the results of positron emission tomography effect of Quetiapine on serotonin 5HT2- and dopamine D2-receptors can be extended to 12 h. Quetiapine is a psychotropic agent belonging to the chemical class of benzisoxazole derivatives and is indicated for the treatment of schizophrenia. Quetiapine is a selective monoaminergic antagonist with high affinity for the serotonin Type 2 (5HT, dopamine D1 and D2, histamine H1, and adrenergic alpha 1 and alpha 2 receptors. Quetiapine has no significant affinity for cholinergic muscarinic or benzodiazepine receptors. Drowsiness and orthostatic hypotension associated with use of Quetiapine may be explained by its antagonism of histamine H1 and adrenergic alpha 1 receptors, respectively. Quetiapine\'s antagonism of adrenergic a1 receptors may explain the orthostatic hypotension observed with this drug. Quetiapine is used to treat schizophrenia and bipolar disorder (manic-depressive disorder). It helps to relieve symptoms common in schizophrenia and bipolar disorder, such as distorted thinking and emotional instability. Quetiapine is also used together with other medicines to treat depression.
更新日期: 2013-11-03
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