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AQUPLA for Intravenous Injection(奈达铂注射剂)

2012-12-02 07:47:01  作者:新特药房  来源:互联网  浏览次数:186  文字大小:【】【】【
简介: 部分中文奈达铂处方资料(仅供参考) 分类名称 一级分类:抗肿瘤药物 二级分类:其他抗肿瘤药物 三级分类: 药品英文名 Nedaplatin 药品别名 Nedaplait、Aqupla 药物剂型 注射用奈达铂:10mg,50 ...

部份中文奈达铂/アクプラ静注用处方资料(仅供参考)
奈达铂(nedaplatin/Aqupla):1995年6月在日本上市,为盐野义制药公司开发的第一个二代铂类抗肿瘤药,每4周1次1小时静脉输注80~100mg/m2,用于治疗头颈部肿瘤、小细胞和非小细胞肺癌、食道癌、膀胱癌、睾丸癌、卵巢癌和子宫颈癌。其疗效优于顺铂,血液学毒性较顺铂高,而肾毒性和胃肠道副反应则较低。
治疗类别名称
抗肿瘤药
药理作用
本药为顺铂类似物,以与顺铂相同的方式与脱氧核糖核酸(DNA)结合,抑制DNA复制,从而产生抗肿瘤活性。其作用机制为:当其进入细胞后,甘醇酸脂配基上的醇性氧与铂之间的键断裂,水与铂结合,形成离子型物质(活性物质或水合物),而断裂的甘醇酸脂配基被释放,产生多种离子型物质并与DNA结合,且结合的碱基位点与顺铂相同。本药与卡铂的优劣比较及适应证的差异,尚缺乏充分研究。
适应症
头颈部癌、小细胞肺癌、非小细胞肺癌、食道癌、膀胱癌、睾丸癌、卵巢癌、子宫颈癌。
用法用量
1.成年人每天一次给药的80-100毫克/米2(体表面积),为奈达铂,随后停药至少4周。这是一个疗程,重复给药。
此外,该剂量可根据年龄,疾病和症状进行调整。
2.这种药物的给药,溶解在一个更生理盐水或5%木糖醇注射溶液的300mL按照给药量,在一个60分钟内静脉内输注。
3.继续成1000mL以上的输液这种药物的管理,以静脉滴注。
AQUPLA for Intravenous Injection(Nedaplatin)

アクプラ静注用10mg/アクプラ静注用50mg/アクプラ静注用100mg

AQUPLA for Intravenous Injection 10mg(アクプラ静注用10mg) 
Brand name : AQUPLA for Intravenous Injection 10mg
 Active ingredient: Nedaplatin
 Dosage form: injection
 Print on wrapping:
AQUPLA for Intravenous Injection 50mg(アクプラ静注用50mg) 
Brand name : AQUPLA for Intravenous Injection 50mg
 Active ingredient: Nedaplatin
 Dosage form: injection
 Print on wrapping:
AQUPLA for Intravenous Injection 100mg(アクプラ静注用100mg)
Brand name : AQUPLA for Intravenous Injection 100mg
 Active ingredient: Nedaplatin
 Dosage form: injection
 Print on wrapping:
Effects of this medicine
This medicine shows antitumor effects by suppressing tumor cell growth due to DNA synthesis inhibition.
It is usually used for the treatment of head and neck cancer, small cell lung cancer, non-small cell lung cancer, esophagus cancer, bladder cancer, testicular tumor, ovarian cancer and uterine cervix cancer.
Before using this medicine, be sure to tell your doctor and pharmacist
•If you have previously experienced any allergic reactions (itch, rash, etc.) to any medicines.
If you have myelosuppression or renal disorder.
•If you are pregnant, possibly pregnant or breastfeeding.
•If you are taking any other medicinal products. (Some medicines may interact to enhance or diminish medicinal effects. Beware of over-the-counter medicines and dietary supplements as well as other prescription medicines.)
Dosing schedule (How to take this medicine)
•Your dosing schedule prescribed by your doctor is <<to be written by a healthcare professional>>
•In general, for adults, this medicine is administered once daily by an intravenous drip infusion over 60 minutes or longer, and then it is discontinued for at least 4 weeks. This dosing schedule as 1 course is repeated.
•After this medicine is used, a transfusion is successively administered by an intravenous drip infusion.
•Consult with your doctor about your concrete schedule for use.
Precautions while taking this medicine
•If you are breastfeeding, discontinue breastfeeding while using this medicine.
Possible adverse reactions to this medicine
The most commonly reported adverse reactions include nausea, vomiting, loss of appetite and hair loss. If any of these symptoms occur, consult with your doctor or pharmacist.
The symptoms described below are rarely seen as initial symptoms of the adverse reactions indicated in brackets. If any of these symptoms occur, stop taking this medicine and see your doctor immediately.
•hot flush, breathing difficulty, chill  [shock, anaphylactoid symptoms]
•fever, symptoms of anemia, bleeding tendency  [myelosuppression]
•swelling, malaise, decreased urine output  [renal failure]
•unable to hear voices and sounds, ear ringing  [deafness, decreased hearing, tinnitus]
•fever, dry cough, breathlessness  [interstitial pneumonia]
The above symptoms do not describe all the adverse reactions to this medicine. Consult with your doctor or pharmacist if you notice any symptoms of concern other than those listed above.
Shionogi & Co., Ltd.Injection
Published: 2/2014
The information on this sheet is based on approvals granted by the Japanese regulatory authority. Approval details may vary by country. Medicines have adverse reactions (risks) as well as efficacies (benefits). It is important to minimize adverse reactions and maximize efficacy. To obtain a better therapeutic response, patients should understand their medication and cooperate with the treatment.
http://www.info.pmda.go.jp/go/pack/4291405F1025_1_10/
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注:以下产品来同规格和不同价格,采购咨询为准!
---------------------------------------------
产地国家:日本
原产地英文商品名:
AQUPLA for Intravenous Injection(アクプラ静注用) 100MG/VIAL
原产地英文药品名:
NEDAPLATIN
原产地英文化合物名称:
cis-Diammineglycolatoplatinum
中文参考商品译名:
AQUPLA(アクプラ静注用) 100毫克/瓶
中文参考药品译名:
奈达铂
生产厂家中文参考译名:
塩野義製薬
生产厂家英文名:
shionogi


-------------------------------------------
产地国家:日本
原产地英文商品名:
AQUPLA for Intravenous Injection(アクプラ静注用) 10MG/VIAL
原产地英文药品名:
NEDAPLATIN
原产地英文化合物名称:
cis-Diammineglycolatoplatinum
中文参考商品译名:
AQUPLA(アクプラ静注用) 10毫克/瓶
中文参考药品译名:
奈达铂
生产厂家中文参考译名:
塩野義製薬
生产厂家英文名:
shionogi


--------------------------------------------
产地国家:日本
原产地英文商品名:
AQUPLA for Intravenous Injection(アクプラ静注用) 50MG/VIAL
原产地英文药品名:
NEDAPLATIN
原产地英文化合物名称:
cis-Diammineglycolatoplatinum
中文参考商品译名:
AQUPLA(アクプラ静注用) 50毫克/瓶
中文参考药品译名:
奈达铂
生产厂家中文参考译名:
塩野義製薬
生产厂家英文名:
shionogi

责任编辑:admin


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