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  药店国别: 日本药房
产地国家: 日本
所属类别: 维生素类及微量元素药物->氨基酸
处方药:保健药品
包装规格: 200毫升 10包/盒
计价单位:
   
生产厂家英文名:
Fusou
原产地英文商品名:
Pleamin-P Injection 200ml 10 bags
原产地英文药品名:
Pediatric Compound Amino Acid Injection
中文参考商品译名:
Pleamin-P 注射剂 200毫升 10包/盒
原产地国家批准上市年份:
0000/00/00
英文适应病症1:
newborn
英文适应病症2:
Hypoproteinemia
英文适应病症3:
malnutrition
英文适应病症4:
before and after surgery
临床试验期:
完成
中文适应病症参考翻译1:
新生儿
中文适应病症参考翻译2:
低蛋白血症
中文适应病症参考翻译3:
营养不良
中文适应病症参考翻译4:
手术前后
药品信息:
效果或疗效 用于氨基酸补充剂的1-3年和婴儿新生儿以下状态。然而,新生儿和重2kg以上在出生作为一般规则。 低蛋白血症,营养不良,手术前后 剂量和用法 通常情况下, (体重超过2公斤出生)和新生儿作为氨基酸/ kg体重/天的量( 23 ~ 36毫升本文) 1.75 ~ 2.75克, 1-3年1.50婴儿~ 2.50克(本文中,我坚持用高热量的方法, 20 ~ 33ML ) /公斤体重/天灌入静脉滴注。 此外,我会根据临床症状,临床化验值进行调整。 注意事项 细心管理 (它应慎用于下列患者进行管理。 ) 1 。 可加重酸中毒患者中毒程度高。 ] 2 。 可加重了心脏衰竭治疗充血性心脏衰竭。 ] 3 。 可加重低钠血症的[此药并不包括大多数娜患者低钠血症。 ] 副作用 的副作用,如概述表达状况 预先核准3箱子婴儿168箱子副作用的报道中( 1.8 % )的调查, 3 ( GPT )升高ALT含量2 ( GOT ), AST升高( 1.2 % ) ( 1.8 % ) , 1铝-P增加( 0.6 % ) (批准) 。 在上市后监测(药物使用调查,特别调查) ,共报告27案件994例( 2.7 % )的副作用。 4直接胆红素主要种的副作用, 6肝功能异常6 ( GPT ) ALT升高9的评论( GOT ), AST升高( 0.9 % ) ( 0.6 % ) ( 0.6 % ) ( 0.4 %)是(复试在结束) 。 其他副作用 1 。过敏症 频率未知 (皮疹等) 2 。消化系统 频率未知 (恶心,呕吐等) 3 。心血管 频率未知 (胸部不适,心悸等) 4 。肝脏 小于0.1-5% 黄疸(胆红素) ,增加AST( GOT) · ALT的(GPT ) ·阿尔-P 5 。质量 - 快速给药 频率未知 (该酸中毒质量 - 快速给药) 6 。他人 频率未知 (寒战,高热,头痛) 如果副作用观察到,这是适当的措施,如中止给药。 未知频率( ) :再评价结果, 15 ( 1979) ,由总氨基酸配方部分。 政府当局的孩子,等等。 (不足临床)尚未确定。安全性低出生体重儿出生时体重低于2公斤。 只有当确定治疗的好处是比我们的低出生体重儿净重2kg ,超越出身,原来少好风险,并适当地增加或减少剂量的临床症状,临床检验值,要谨慎服用。 另外994例,其中收集的(药物使用调查,特别调查)上市后监测,低出生体重儿体重的情况下, 2kg以下的比出生时为293例,副作用10箱子( 3.4 %)为报道他们。 3直接胆红素升高4 ( GOT ), AST升高( 1.4 % ) ( 1.0 % ) , 2条评论ALT (谷丙转氨酶)主要类型的副作用上涨( 0.7 % ) Effect or efficacy Is used for amino acid supplementation following state in newborn infants , of 1-3 years and infants . However , newborn and weight 2kg or more at birth as a general rule . Hypoproteinemia , malnutrition , before and after surgery Dosage and usage Usually , ( body weight more than 2kg at birth ) and newborn infants as the amount of amino acid / kg body weight / day (23 ~ 36mL this article ) 1.75 ~ 2.75g, the infants of 1-3 years 1.50 ~ 2.50g ( this article I persist instilled into the intravenous infusion by high-calorie method 20 ~ 33mL) / kg body weight / day . In addition , I will be adjusted according to clinical symptoms , clinical laboratory values ​​. PRECAUTIONS Careful administration ( It should be administered with caution in the following patients. ) 1 . May be aggravated the acidosis patients with a high degree of acidosis . ] 2 . May be aggravated the heart failure patients with congestive heart failure . ] 3 . May be aggravated hyponatremia for [ this drug does not include most of the Na patients with hyponatremia . ] Side effect Overview of side effects such as expression situation A survey of pre-approval three cases infant 168 cases of side effects was reported in the ( 1.8% ) , 3 (GPT) increased ALT contents 2 (GOT) increased AST (1.2%), (1.8%) , 1 Al-P was increased ( 0.6% ) ( approval ) . In post-marketing surveillance ( drug use investigation , Special Investigation ) , 27 cases of side effects in 994 cases ( 2.7% ) were reported . 4 bilirubin direct main kinds of side effects , 6 liver dysfunction 6 (GPT) increased ALT 9 reviews (GOT) increased AST (0.9%), (0.6%), (0.6%), (0.4%) it was ( re-examination at the end ) . Other side effects 1 . Hypersensitivity Frequency unknown ( Rash , etc.) 2 . Digestive Frequency unknown ( Nausea , vomiting , etc.) 3 . Cardiovascular Frequency unknown ( Chest discomfort , palpitations , etc.) 4 . Liver 0.1-5% less than Jaundice ( bilirubin ) , increased AST (GOT) · ALT of (GPT) · Al-P 5 . Mass - rapid administration Frequency unknown ( The acidosis by mass - rapid administration ) 6 . Others Frequency unknown ( Chills , fever , headache ) If side effects are observed, and it is appropriate measures such as discontinuing administration . Of unknown frequency ( ) : re-evaluation result 15 ( 1979 ) , by section of the total amino acid formulation . Administration to children , etc. ( Insufficient clinical ) has not been established. Safety for low birth weight infants weighing less than 2kg at birth . Only when it is determined that therapeutic benefit is better than our original risk for low birth weight infants weighing 2kg less than birth , and be appropriately increased or decreased the dose clinical symptoms , clinical laboratory values ​​, to be administered with caution . In addition , 994 cases in which were collected post-marketing surveillance in ( drug use investigation , Special Investigation ) , low birth weight infants cases of body weight 2kg less than at birth is 293 cases , side effects 10 cases of (3.4 %) were reported them . 3 direct bilirubin rise 4 (GOT) increased AST (1.4%), (1.0%), 2 reviews ALT (GPT) rising main types of side effects ( 0.7% )
更新日期: 2013-10-28
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