NovoRapid

Riik: Euroopa Liit

keel: inglise

Allikas: EMA (European Medicines Agency)

Osta kohe

Infovoldik Infovoldik (PIL)
22-03-2023
Toote omadused Toote omadused (SPC)
22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande (PAR)
15-11-2016

Toimeaine:

insulin aspart

Saadav alates:

Novo Nordisk A/S

ATC kood:

A10AB05

INN (Rahvusvaheline Nimetus):

insulin aspart

Terapeutiline rühm:

Drugs used in diabetes

Terapeutiline ala:

Diabetes Mellitus

Näidustused:

NovoRapid is indicated for treatment of diabetes mellitus in adults, adolescents and children aged 1 year and above.

Toote kokkuvõte:

Revision: 32

Volitamisolek:

Authorised

Loa andmise kuupäev:

1999-09-07

Infovoldik

                                56
B. PACKAGE LEAFLET
57
PACKAGE LEAFLET: INFORMATION FOR THE USER
NOVORAPID 100 UNITS/ML SOLUTION FOR INJECTION IN VIAL
insulin aspart
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START USING THIS
MEDICINE BECAUSE IT CONTAINS
IMPORTANT INFORMATION FOR YOU.
•
Keep this leaflet. You may need to read it again.
•
If you have any further questions, ask your doctor, nurse or
pharmacist.
•
This medicine has been prescribed for you only. Do not pass it on to
others. It may harm them,
even if their signs of illness are the same as yours.
•
If you get any side effects, talk with your doctor, nurse or
pharmacist. This includes any
possible side effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What NovoRapid is and what it is used for
2.
What you need to know before you use NovoRapid
3.
How to use NovoRapid
4.
Possible side effects
5.
How to store NovoRapid
6.
Contents of the pack and other information
1.
WHAT NOVORAPID IS AND WHAT IT IS USED FOR
NovoRapid is a modern insulin (insulin analogue) with a rapid-acting
effect. Modern insulin products
are improved versions of human insulin.
NovoRapid is used to reduce the high blood sugar level in adults,
adolescents and children aged 1 year
and above with diabetes mellitus (diabetes). Diabetes is a disease
where your body does not produce
enough insulin to control the level of your blood sugar. Treatment
with NovoRapid helps to prevent
complications from your diabetes.
NovoRapid will start to lower your blood sugar 10–20 minutes after
you inject it, a maximum effect
occurs between 1 and 3 hours after the injection and the effect lasts
for 3–5 hours. Due to this short
action NovoRapid should normally be taken in combination with
intermediate-acting or long-acting
insulin preparations. Moreover NovoRapid can be used for continuous
infusion in a pump system.
2.
WHAT YOU NEED TO KNOW BEFORE YOU USE NOVORAPID
DO NOT USE NOVORAPID
►
If you are allergic to insulin aspart, or any of the other ingredients
in this medicine (see section
6, Conten
                                
                                Lugege kogu dokumenti
                                
                            

Toote omadused

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
NovoRapid 100 units/ml solution for injection in vial
NovoRapid Penfill 100 units/ml solution for injection in cartridge
NovoRapid FlexPen 100 units/ml solution for injection in pre-filled
pen
NovoRapid InnoLet 100 units/ml solution for injection in pre-filled
pen
NovoRapid FlexTouch 100 units/ml solution for injection in pre-filled
pen
NovoRapid PumpCart 100 units/ml solution for injection in cartridge
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
NovoRapid vial
1 vial contains 10 ml equivalent to 1,000 units.1 ml solution contains
100 units insulin aspart*
(equivalent to 3.5 mg).
NovoRapid Penfill
1 cartridge contains 3 ml equivalent to 300 units.1 ml solution
contains 100 units insulin aspart*
(equivalent to 3.5 mg).
NovoRapid FlexPen/NovoRapid InnoLet/NovoRapid FlexTouch
1 pre-filled pen contains 3 ml equivalent to 300 units.1 ml solution
contains 100 units insulin aspart*
(equivalent to 3.5 mg).
NovoRapid PumpCart
1 cartridge contains 1.6 ml equivalent to 160 units.1 ml solution
contains 100 units insulin aspart*
(equivalent to 3.5 mg).
*Insulin aspart is produced in
_Saccharomyces cerevisiae _
by recombinant DNA technology.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Solution for injection.
The solution is clear, colourless and aqueous.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
NovoRapid is indicated for treatment of diabetes mellitus in adults,
adolescents and children aged 1
year and above.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
POSOLOGY
The potency of insulin analogues, including insulin aspart, is
expressed in units, whereas the potency
of human insulin is expressed in international units.
NovoRapid dosing is individual and determined in accordance with the
needs of the patient. It should
normally be used in combination with intermediate-acting or
long-acting insulin.
3
Moreover NovoRapid vial and NovoRapid PumpCart can be used for
continuous subcutaneous insulin
infusion (CSII) in pum
                                
                                Lugege kogu dokumenti
                                
                            

Dokumendid teistes keeltes

Infovoldik Infovoldik bulgaaria 22-03-2023
Toote omadused Toote omadused bulgaaria 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande bulgaaria 15-11-2016
Infovoldik Infovoldik hispaania 22-03-2023
Toote omadused Toote omadused hispaania 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande hispaania 15-11-2016
Infovoldik Infovoldik tšehhi 22-03-2023
Toote omadused Toote omadused tšehhi 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande tšehhi 15-11-2016
Infovoldik Infovoldik taani 22-03-2023
Toote omadused Toote omadused taani 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande taani 15-11-2016
Infovoldik Infovoldik saksa 22-03-2023
Toote omadused Toote omadused saksa 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande saksa 15-11-2016
Infovoldik Infovoldik eesti 22-03-2023
Toote omadused Toote omadused eesti 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande eesti 15-11-2016
Infovoldik Infovoldik kreeka 22-03-2023
Toote omadused Toote omadused kreeka 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande kreeka 15-11-2016
Infovoldik Infovoldik prantsuse 22-03-2023
Toote omadused Toote omadused prantsuse 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande prantsuse 15-11-2016
Infovoldik Infovoldik itaalia 22-03-2023
Toote omadused Toote omadused itaalia 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande itaalia 15-11-2016
Infovoldik Infovoldik läti 22-03-2023
Toote omadused Toote omadused läti 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande läti 15-11-2016
Infovoldik Infovoldik leedu 22-03-2023
Toote omadused Toote omadused leedu 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande leedu 15-11-2016
Infovoldik Infovoldik ungari 22-03-2023
Toote omadused Toote omadused ungari 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande ungari 15-11-2016
Infovoldik Infovoldik malta 22-03-2023
Toote omadused Toote omadused malta 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande malta 15-11-2016
Infovoldik Infovoldik hollandi 22-03-2023
Toote omadused Toote omadused hollandi 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande hollandi 15-11-2016
Infovoldik Infovoldik poola 22-03-2023
Toote omadused Toote omadused poola 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande poola 15-11-2016
Infovoldik Infovoldik portugali 22-03-2023
Toote omadused Toote omadused portugali 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande portugali 15-11-2016
Infovoldik Infovoldik rumeenia 22-03-2023
Toote omadused Toote omadused rumeenia 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande rumeenia 15-11-2016
Infovoldik Infovoldik slovaki 22-03-2023
Toote omadused Toote omadused slovaki 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande slovaki 15-11-2016
Infovoldik Infovoldik sloveeni 22-03-2023
Toote omadused Toote omadused sloveeni 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande sloveeni 15-11-2016
Infovoldik Infovoldik soome 22-03-2023
Toote omadused Toote omadused soome 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande soome 15-11-2016
Infovoldik Infovoldik rootsi 22-03-2023
Toote omadused Toote omadused rootsi 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande rootsi 15-11-2016
Infovoldik Infovoldik norra 22-03-2023
Toote omadused Toote omadused norra 22-03-2023
Infovoldik Infovoldik islandi 22-03-2023
Toote omadused Toote omadused islandi 22-03-2023
Infovoldik Infovoldik horvaadi 22-03-2023
Toote omadused Toote omadused horvaadi 22-03-2023
Avaliku hindamisaruande Avaliku hindamisaruande horvaadi 15-11-2016

Otsige selle tootega seotud teateid

Vaadake dokumentide ajalugu