Insulin Human Winthrop

国家: 欧盟

语言: 英文

来源: EMA (European Medicines Agency)

现在购买

资料单张 资料单张 (PIL)
30-04-2018
产品特点 产品特点 (SPC)
30-04-2018
公众评估报告 公众评估报告 (PAR)
30-04-2018

有效成分:

Insulin human

可用日期:

sanofi-aventis Deutschland GmbH

ATC代码:

A10AB01

INN(国际名称):

insulin human

治疗组:

Drugs used in diabetes

治疗领域:

Diabetes Mellitus

疗效迹象:

Diabetes mellitus where treatment with insulin is required. Insulin Human Winthrop Rapid is also suitable for the treatment of hyperglycaemic coma and ketoacidosis, as well as for achieving pre-, intra- and postoperative stabilisation in patients with diabetes mellitus.

產品總結:

Revision: 15

授权状态:

Withdrawn

授权日期:

2007-01-17

资料单张

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
Medicinal product no longer authorised
2
1.
NAME OF THE MEDICINAL PRODUCT
_ _
Insulin Human Winthrop Rapid 100 IU/ml solution for injection in a
vial
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each ml contains 100 IU insulin human (equivalent to 3.5 mg).
Each vial contains 5 ml of solution for injection, equivalent to 500
IU insulin, or 10 ml of solution for
injection, equivalent to 1000 IU insulin. One IU (International Unit)
corresponds to 0.035 mg of
anhydrous human insulin.
Insulin Human Winthrop Rapid is a neutral insulin solution (regular
insulin).
Human insulin is produced by recombinant DNA technology in
_Escherichia coli_
.
For the full list of excipients, see section 6.1.
_ _
3.
PHARMACEUTICAL FORM
Solution for injection in a vial.
Clear, colourless solution.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Diabetes mellitus where treatment with insulin is required. Insulin
Human Winthrop Rapid is also
suitable for the treatment of hyperglycaemic coma and ketoacidosis, as
well as for achieving pre-,
intra- and post-operative stabilisation in patients with diabetes
mellitus.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
The desired blood glucose levels, the insulin preparations to be used
and the insulin dose regimen
(doses and timings) must be determined individually and adjusted to
suit the patient’s diet, physical
activity and life-style.
_Daily doses and timing of administration _
There are no fixed rules for insulin dose regimen. However, the
average insulin requirement is often
0.5 to 1.0 IU per kg body weight per day. The basal metabolic
requirement is 40% to 60% of the total
daily requirement. Insulin Human Winthrop Rapid is injected
subcutaneously 15 to 20 minutes before
a meal.
In the treatment of severe hyperglycaemia or ketoacidosis in
particular, insulin administration is part
of a complex therapeutic regimen which includes measures to protect
patients from possible severe
complications of a relatively rapid lowering of blood glucose. T
                                
                                阅读完整的文件
                                
                            

产品特点

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
Medicinal product no longer authorised
2
1.
NAME OF THE MEDICINAL PRODUCT
_ _
Insulin Human Winthrop Rapid 100 IU/ml solution for injection in a
vial
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each ml contains 100 IU insulin human (equivalent to 3.5 mg).
Each vial contains 5 ml of solution for injection, equivalent to 500
IU insulin, or 10 ml of solution for
injection, equivalent to 1000 IU insulin. One IU (International Unit)
corresponds to 0.035 mg of
anhydrous human insulin.
Insulin Human Winthrop Rapid is a neutral insulin solution (regular
insulin).
Human insulin is produced by recombinant DNA technology in
_Escherichia coli_
.
For the full list of excipients, see section 6.1.
_ _
3.
PHARMACEUTICAL FORM
Solution for injection in a vial.
Clear, colourless solution.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Diabetes mellitus where treatment with insulin is required. Insulin
Human Winthrop Rapid is also
suitable for the treatment of hyperglycaemic coma and ketoacidosis, as
well as for achieving pre-,
intra- and post-operative stabilisation in patients with diabetes
mellitus.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
The desired blood glucose levels, the insulin preparations to be used
and the insulin dose regimen
(doses and timings) must be determined individually and adjusted to
suit the patient’s diet, physical
activity and life-style.
_Daily doses and timing of administration _
There are no fixed rules for insulin dose regimen. However, the
average insulin requirement is often
0.5 to 1.0 IU per kg body weight per day. The basal metabolic
requirement is 40% to 60% of the total
daily requirement. Insulin Human Winthrop Rapid is injected
subcutaneously 15 to 20 minutes before
a meal.
In the treatment of severe hyperglycaemia or ketoacidosis in
particular, insulin administration is part
of a complex therapeutic regimen which includes measures to protect
patients from possible severe
complications of a relatively rapid lowering of blood glucose. T
                                
                                阅读完整的文件
                                
                            

其他语言的文件

资料单张 资料单张 保加利亚文 30-04-2018
产品特点 产品特点 保加利亚文 30-04-2018
公众评估报告 公众评估报告 保加利亚文 30-04-2018
资料单张 资料单张 西班牙文 30-04-2018
产品特点 产品特点 西班牙文 30-04-2018
公众评估报告 公众评估报告 西班牙文 30-04-2018
资料单张 资料单张 捷克文 30-04-2018
产品特点 产品特点 捷克文 30-04-2018
公众评估报告 公众评估报告 捷克文 30-04-2018
资料单张 资料单张 丹麦文 30-04-2018
产品特点 产品特点 丹麦文 30-04-2018
公众评估报告 公众评估报告 丹麦文 30-04-2018
资料单张 资料单张 德文 30-04-2018
产品特点 产品特点 德文 30-04-2018
公众评估报告 公众评估报告 德文 30-04-2018
资料单张 资料单张 爱沙尼亚文 30-04-2018
产品特点 产品特点 爱沙尼亚文 30-04-2018
公众评估报告 公众评估报告 爱沙尼亚文 30-04-2018
资料单张 资料单张 希腊文 30-04-2018
产品特点 产品特点 希腊文 30-04-2018
公众评估报告 公众评估报告 希腊文 30-04-2018
资料单张 资料单张 法文 30-04-2018
产品特点 产品特点 法文 30-04-2018
公众评估报告 公众评估报告 法文 30-04-2018
资料单张 资料单张 意大利文 30-04-2018
产品特点 产品特点 意大利文 30-04-2018
公众评估报告 公众评估报告 意大利文 30-04-2018
资料单张 资料单张 拉脱维亚文 30-04-2018
产品特点 产品特点 拉脱维亚文 30-04-2018
公众评估报告 公众评估报告 拉脱维亚文 30-04-2018
资料单张 资料单张 立陶宛文 30-04-2018
产品特点 产品特点 立陶宛文 30-04-2018
公众评估报告 公众评估报告 立陶宛文 30-04-2018
资料单张 资料单张 匈牙利文 30-04-2018
产品特点 产品特点 匈牙利文 30-04-2018
公众评估报告 公众评估报告 匈牙利文 30-04-2018
资料单张 资料单张 马耳他文 30-04-2018
产品特点 产品特点 马耳他文 30-04-2018
公众评估报告 公众评估报告 马耳他文 30-04-2018
资料单张 资料单张 荷兰文 30-04-2018
产品特点 产品特点 荷兰文 30-04-2018
公众评估报告 公众评估报告 荷兰文 30-04-2018
资料单张 资料单张 波兰文 30-04-2018
产品特点 产品特点 波兰文 30-04-2018
公众评估报告 公众评估报告 波兰文 30-04-2018
资料单张 资料单张 葡萄牙文 30-04-2018
产品特点 产品特点 葡萄牙文 30-04-2018
公众评估报告 公众评估报告 葡萄牙文 30-04-2018
资料单张 资料单张 罗马尼亚文 30-04-2018
产品特点 产品特点 罗马尼亚文 30-04-2018
公众评估报告 公众评估报告 罗马尼亚文 30-04-2018
资料单张 资料单张 斯洛伐克文 30-04-2018
产品特点 产品特点 斯洛伐克文 30-04-2018
公众评估报告 公众评估报告 斯洛伐克文 30-04-2018
资料单张 资料单张 斯洛文尼亚文 30-04-2018
产品特点 产品特点 斯洛文尼亚文 30-04-2018
公众评估报告 公众评估报告 斯洛文尼亚文 30-04-2018
资料单张 资料单张 芬兰文 30-04-2018
产品特点 产品特点 芬兰文 30-04-2018
公众评估报告 公众评估报告 芬兰文 30-04-2018
资料单张 资料单张 瑞典文 30-04-2018
产品特点 产品特点 瑞典文 30-04-2018
公众评估报告 公众评估报告 瑞典文 30-04-2018
资料单张 资料单张 挪威文 30-04-2018
产品特点 产品特点 挪威文 30-04-2018
资料单张 资料单张 冰岛文 30-04-2018
产品特点 产品特点 冰岛文 30-04-2018
资料单张 资料单张 克罗地亚文 30-04-2018
产品特点 产品特点 克罗地亚文 30-04-2018

搜索与此产品相关的警报