Wednesday, December 5, 2012

Tationil 900mg / 4ml ( bayer )







composition
Tationil 600mg: 1 vial of powder for solution for injection contains glutathione (sodium salt) 600mg. 1 vial of solvent contains: 3 ml water for injections.
Tationil 900mg: 1 vial of powder for solution for injection contains glutathione (sodium salt) 900mg. 1 vial of solution contains: water for injections 4 ml.

Pharmaceutical form and contents
5 vials + 5 vials 600mg powder 3 ml solvent.
10 vials powder 600mg + 10 ampoules of solvent 3 ml.
5 vials + 5 vials 900mg powder 4 ml solvent.
10 vials powder 900mg + 10 ampoules of solvent 4 ml.

Pharmacotherapeutic
antidotes

Name and address of the owner of 'authorization to' marketing
Marketing Authorisation Holder: Bayer SpA - Viale charterhouses 130-20156 Milan.

Name and address of the manufacturer
Tationil 600mg/3ml powder and solvent for solution for injection produced and controlled by Patheon Italy SpA.
officinadi Monza (MI) - Via G.B. Stucchi 110.

Tationil 900mg/4ml powder and solvent for solution for injection vials powder produced and controlled by Patheon Italy SpA.
workshop Monza (MI)-Viale G.B. Stucchi 110; Patheon S.p.A. Italy.
-workshop ferentino (FR) - Via Morolense 87.
Ampoules of solvent: product and controlled by Patheon Italy SpA.
-workshop Monza (MI)-Viale G.B. Stucchi 110.

therapeutic indications
Prophylaxis of neuropathy resulting from chemotherapy treatment with cisplatin or similar.

Contraindications
Ipersensibilite individually assessed to the drug.

Precautions for use
No.

Use in pregnancy and lactation
Is not recommended for use during pregnancy and breastfeeding.

Effects on driving and use machines
No.

Dose and timing of administration
In mild: 1-2 bottles a day 600mg intramuscularly or intravenously or as otherwise prescribed slow.
In the more demanding forms: 1-2 bottles a day to 900mg intramuscularly, intravenously or added to slow infusion or as otherwise prescribed.

overdose
There are no known cases of overdose.

side effects
May occur very rarely rashes disappear discontinuing therapy.
You should consult your doctor pharmacist in case of occurrence of undesired effects not described in this leaflet.

Mode of preservation
Caution: Do not use the medicine after the expiry date shown on the packaging.




 组成
tationil600毫克:1粉末注射用溶液的小瓶含有还原型谷胱甘肽(钠盐)600毫克。 1瓶溶剂含有:3毫升注射用水。
tationil900毫克:1粉末注射用溶液的小瓶含有还原型谷胱甘肽(钠盐)900毫克。 1瓶的解决方案包括:水注射4毫升。

药品的形式和内容
5瓶5瓶600毫克粉3毫升溶剂。
10瓶粉600毫克+溶剂3毫升10支。
5瓶5瓶900毫克粉4毫升溶剂。
10小瓶粉末900毫克+10安瓿溶剂4毫升的。

药物治疗
解毒剂

的名称和地址的所有者的授权营销
上市许可持有人::拜耳SPA - 130-20156米兰的Viale charterhouses

的制造商的名称和地址
tationil600mg/3ml注射用溶液的粉末和溶剂生产和由Patheon意大利SpA的控制。
officinadi蒙扎(MI) - 通过G.B.斯图基110。

tationil900mg/4ml粉末和溶剂的溶液用注射小瓶粉末生产和由Patheon意大利SpA的控制。
车间蒙扎(MI)的Viale G.B.斯图基110 Patheon S.p.A.的意大利。
-:车间ferentino(FR) - 通过Morolense87中。
安瓶的溶剂产品和Patheon意大利水疗控制。
车间蒙扎(MI)的Viale G.B.斯图基110。


 治疗适应症
导致神经病变的预防与顺铂或类似化疗治疗。

禁忌
Ipersensibilite个别方式评估的药物。

使用注意事项


在怀孕和哺乳期的使用
在怀孕和哺乳期间不建议使用。

驾驶及使用机器


剂量和给药时间
轻度:1-2瓶,每天600毫克肌肉注射或静脉注射或另有规定缓慢。
在要求更高的形式:每天1-2瓶900毫克肌肉注射,静脉注射或缓慢滴注,或另有规定。

过量
有没有已知的情况下,过量。

副作用
可能很少发生皮疹消失,停止治疗。
您应该咨询你的医生,药剂师,以防发生意外的影响没有说明这本小册子。

的保存方式
注意:不要使用药物后的包装上显示的有效期。


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