Jivi

Land: Europeiska unionen

Språk: engelska

Källa: EMA (European Medicines Agency)

Köp det nu

Bipacksedel Bipacksedel (PIL)
13-07-2023
Produktens egenskaper Produktens egenskaper (SPC)
13-07-2023

Aktiva substanser:

Damoctocog alfa pegol

Tillgänglig från:

Bayer AG

ATC-kod:

B02BD02

INN (International namn):

damoctocog alfa pegol

Terapeutisk grupp:

Antihemorrhagics

Terapiområde:

Hemophilia A

Terapeutiska indikationer:

Treatment and prophylaxis of bleeding in previously treated patients ≥ 12 years of age with haemophilia A (congenital factor VIII deficiency).

Produktsammanfattning:

Revision: 5

Bemyndigande status:

Authorised

Tillstånd datum:

2018-11-22

Bipacksedel

                                73
B. PACKAGE LEAFLET
74
PACKAGE LEAFLET: INFORMATION FOR THE USER
JIVI 250 IU POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
JIVI 500 IU POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
JIVI 1000 IU POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
JIVI 2000 IU POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
JIVI 3000 IU POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
PEGylated B-domain deleted recombinant human coagulation factor VIII
(damoctocog alfa pegol)
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 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 to your doctor or pharmacist. This
includes any possible side
effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Jivi is and what it is used for
2.
What you need to know before you use Jivi
3.
How to use Jivi
4.
Possible side effects
5.
How to store Jivi
6.
Contents of the pack and other information
1.
WHAT JIVI IS AND WHAT IT IS USED FOR
Jivi contains the active substance damoctocog alfa pegol. It is
produced by recombinant technology
without addition of any human- or animal-derived components in the
manufacturing process.
Factor VIII is a protein naturally found in the blood that helps to
clot it. The protein in damoctocog
alfa pegol has been modified (pegylated) to prolong its action in the
body.
Jivi is used to TREAT AND PREVENT BLEEDING in previously treated
adults and adolescents aged from
12 years with haemophilia A (hereditary factor VIII deficiency). It is
not for use in children younger
than 12 years of age.
2.
WHAT YOU NEED TO KNOW BEFORE YOU USE JIVI
DO NOT USE JIVI if you are
•
allergic to damoctocog alfa pegol or any of the other ingredients of
this medicine (listed in
section 6).
•
allergic to mou
                                
                                Läs hela dokumentet
                                
                            

Produktens egenskaper

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Jivi 250 IU powder and solvent for solution for injection
Jivi 500 IU powder and solvent for solution for injection
Jivi 1000 IU powder and solvent for solution for injection
Jivi 2000 IU powder and solvent for solution for injection
Jivi 3000 IU powder and solvent for solution for injection
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Jivi 250 IU powder and solvent for solution for injection
After reconstitution with the solvent provided, one mL of solution
contains approximately 100 IU
(250 IU/2.5 mL) of human coagulation factor VIII, damoctocog alfa
pegol.
Jivi 500 IU powder and solvent for solution for injection
After reconstitution with the solvent provided, one mL of solution
contains approximately 200 IU
(500 IU/2.5 mL) of human coagulation factor VIII, damoctocog alfa
pegol.
Jivi 1000 IU powder and solvent for solution for injection
After reconstitution with the solvent provided, one mL of solution
contains approximately 400 IU
(1 000 IU/2.5 mL) of human coagulation factor VIII, damoctocog alfa
pegol.
Jivi 2000 IU powder and solvent for solution for injection
After reconstitution with the solvent provided, one mL of solution
contains approximately 800 IU
(2 000 IU/2.5 mL) of human coagulation factor VIII, damoctocog alfa
pegol.
Jivi 3000 IU powder and solvent for solution for injection
After reconstitution with the solvent provided, one mL of solution
contains approximately 1 200 IU
(3 000 IU/2.5 mL) of human coagulation factor
VIII, damoctocog alfa pegol.
The potency International Unit (IU) is determined using the European
Pharmacopoeia chromogenic
assay. The specific activity of Jivi is approximately 10 000 IU/mg
protein.
The active substance, damoctocog alfa pegol, is a site specifically
PEGylated B-domain deleted
recombinant human coagulation factor VIII, produced in baby hamster
kidney cells (BHK), with a
60 kDa branched polyethylene-glycol (two 30 kDa PEG) moiety. The
molecular weight of the protein
is approximately 234 k
                                
                                Läs hela dokumentet
                                
                            

Dokument på andra språk

Bipacksedel Bipacksedel bulgariska 13-07-2023
Produktens egenskaper Produktens egenskaper bulgariska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport bulgariska 28-01-2019
Bipacksedel Bipacksedel spanska 13-07-2023
Produktens egenskaper Produktens egenskaper spanska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport spanska 28-01-2019
Bipacksedel Bipacksedel tjeckiska 13-07-2023
Produktens egenskaper Produktens egenskaper tjeckiska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport tjeckiska 28-01-2019
Bipacksedel Bipacksedel danska 13-07-2023
Produktens egenskaper Produktens egenskaper danska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport danska 28-01-2019
Bipacksedel Bipacksedel tyska 13-07-2023
Produktens egenskaper Produktens egenskaper tyska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport tyska 28-01-2019
Bipacksedel Bipacksedel estniska 13-07-2023
Produktens egenskaper Produktens egenskaper estniska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport estniska 28-01-2019
Bipacksedel Bipacksedel grekiska 13-07-2023
Produktens egenskaper Produktens egenskaper grekiska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport grekiska 28-01-2019
Bipacksedel Bipacksedel franska 13-07-2023
Produktens egenskaper Produktens egenskaper franska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport franska 28-01-2019
Bipacksedel Bipacksedel italienska 13-07-2023
Produktens egenskaper Produktens egenskaper italienska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport italienska 28-01-2019
Bipacksedel Bipacksedel lettiska 13-07-2023
Produktens egenskaper Produktens egenskaper lettiska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport lettiska 28-01-2019
Bipacksedel Bipacksedel litauiska 13-07-2023
Produktens egenskaper Produktens egenskaper litauiska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport litauiska 28-01-2019
Bipacksedel Bipacksedel ungerska 13-07-2023
Produktens egenskaper Produktens egenskaper ungerska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport ungerska 28-01-2019
Bipacksedel Bipacksedel maltesiska 13-07-2023
Produktens egenskaper Produktens egenskaper maltesiska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport maltesiska 28-01-2019
Bipacksedel Bipacksedel nederländska 13-07-2023
Produktens egenskaper Produktens egenskaper nederländska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport nederländska 28-01-2019
Bipacksedel Bipacksedel polska 13-07-2023
Produktens egenskaper Produktens egenskaper polska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport polska 28-01-2019
Bipacksedel Bipacksedel portugisiska 13-07-2023
Produktens egenskaper Produktens egenskaper portugisiska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport portugisiska 28-01-2019
Bipacksedel Bipacksedel rumänska 13-07-2023
Produktens egenskaper Produktens egenskaper rumänska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport rumänska 28-01-2019
Bipacksedel Bipacksedel slovakiska 13-07-2023
Produktens egenskaper Produktens egenskaper slovakiska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport slovakiska 28-01-2019
Bipacksedel Bipacksedel slovenska 13-07-2023
Produktens egenskaper Produktens egenskaper slovenska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport slovenska 28-01-2019
Bipacksedel Bipacksedel finska 13-07-2023
Produktens egenskaper Produktens egenskaper finska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport finska 28-01-2019
Bipacksedel Bipacksedel svenska 13-07-2023
Produktens egenskaper Produktens egenskaper svenska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport svenska 28-01-2019
Bipacksedel Bipacksedel norska 13-07-2023
Produktens egenskaper Produktens egenskaper norska 13-07-2023
Bipacksedel Bipacksedel isländska 13-07-2023
Produktens egenskaper Produktens egenskaper isländska 13-07-2023
Bipacksedel Bipacksedel kroatiska 13-07-2023
Produktens egenskaper Produktens egenskaper kroatiska 13-07-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport kroatiska 28-01-2019

Sök varningar relaterade till denna produkt

Visa dokumenthistorik