Insulin Human Winthrop

Riik: Euroopa Liit

keel: inglise

Allikas: EMA (European Medicines Agency)

Osta kohe

Infovoldik Infovoldik (PIL)
30-04-2018
Toote omadused Toote omadused (SPC)
30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande (PAR)
30-04-2018

Toimeaine:

Insulin human

Saadav alates:

sanofi-aventis Deutschland GmbH

ATC kood:

A10AB01

INN (Rahvusvaheline Nimetus):

insulin human

Terapeutiline rühm:

Drugs used in diabetes

Terapeutiline ala:

Diabetes Mellitus

Näidustused:

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.

Toote kokkuvõte:

Revision: 15

Volitamisolek:

Withdrawn

Loa andmise kuupäev:

2007-01-17

Infovoldik

                                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
                                
                                Lugege kogu dokumenti
                                
                            

Toote omadused

                                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
                                
                                Lugege kogu dokumenti
                                
                            

Dokumendid teistes keeltes

Infovoldik Infovoldik bulgaaria 30-04-2018
Toote omadused Toote omadused bulgaaria 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande bulgaaria 30-04-2018
Infovoldik Infovoldik hispaania 30-04-2018
Toote omadused Toote omadused hispaania 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande hispaania 30-04-2018
Infovoldik Infovoldik tšehhi 30-04-2018
Toote omadused Toote omadused tšehhi 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande tšehhi 30-04-2018
Infovoldik Infovoldik taani 30-04-2018
Toote omadused Toote omadused taani 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande taani 30-04-2018
Infovoldik Infovoldik saksa 30-04-2018
Toote omadused Toote omadused saksa 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande saksa 30-04-2018
Infovoldik Infovoldik eesti 30-04-2018
Toote omadused Toote omadused eesti 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande eesti 30-04-2018
Infovoldik Infovoldik kreeka 30-04-2018
Toote omadused Toote omadused kreeka 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande kreeka 30-04-2018
Infovoldik Infovoldik prantsuse 30-04-2018
Toote omadused Toote omadused prantsuse 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande prantsuse 30-04-2018
Infovoldik Infovoldik itaalia 30-04-2018
Toote omadused Toote omadused itaalia 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande itaalia 30-04-2018
Infovoldik Infovoldik läti 30-04-2018
Toote omadused Toote omadused läti 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande läti 30-04-2018
Infovoldik Infovoldik leedu 30-04-2018
Toote omadused Toote omadused leedu 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande leedu 30-04-2018
Infovoldik Infovoldik ungari 30-04-2018
Toote omadused Toote omadused ungari 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande ungari 30-04-2018
Infovoldik Infovoldik malta 30-04-2018
Toote omadused Toote omadused malta 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande malta 30-04-2018
Infovoldik Infovoldik hollandi 30-04-2018
Toote omadused Toote omadused hollandi 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande hollandi 30-04-2018
Infovoldik Infovoldik poola 30-04-2018
Toote omadused Toote omadused poola 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande poola 30-04-2018
Infovoldik Infovoldik portugali 30-04-2018
Toote omadused Toote omadused portugali 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande portugali 30-04-2018
Infovoldik Infovoldik rumeenia 30-04-2018
Toote omadused Toote omadused rumeenia 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande rumeenia 30-04-2018
Infovoldik Infovoldik slovaki 30-04-2018
Toote omadused Toote omadused slovaki 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande slovaki 30-04-2018
Infovoldik Infovoldik sloveeni 30-04-2018
Toote omadused Toote omadused sloveeni 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande sloveeni 30-04-2018
Infovoldik Infovoldik soome 30-04-2018
Toote omadused Toote omadused soome 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande soome 30-04-2018
Infovoldik Infovoldik rootsi 30-04-2018
Toote omadused Toote omadused rootsi 30-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande rootsi 30-04-2018
Infovoldik Infovoldik norra 30-04-2018
Toote omadused Toote omadused norra 30-04-2018
Infovoldik Infovoldik islandi 30-04-2018
Toote omadused Toote omadused islandi 30-04-2018
Infovoldik Infovoldik horvaadi 30-04-2018
Toote omadused Toote omadused horvaadi 30-04-2018

Otsige selle tootega seotud teateid