Jivi

Country: Evrópusambandið

Tungumál: enska

Heimild: EMA (European Medicines Agency)

Kauptu það núna

Vara einkenni Vara einkenni (SPC)
13-07-2023
Opinber matsskýrsla Opinber matsskýrsla (PAR)
28-01-2019

Virkt innihaldsefni:

Damoctocog alfa pegol

Fáanlegur frá:

Bayer AG

ATC númer:

B02BD02

INN (Alþjóðlegt nafn):

damoctocog alfa pegol

Meðferðarhópur:

Antihemorrhagics

Lækningarsvæði:

Hemophilia A

Ábendingar:

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

Vörulýsing:

Revision: 5

Leyfisstaða:

Authorised

Leyfisdagur:

2018-11-22

Upplýsingar fylgiseðill

                                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
                                
                                Lestu allt skjalið
                                
                            

Vara einkenni

                                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
                                
                                Lestu allt skjalið
                                
                            

Skjöl á öðrum tungumálum

Upplýsingar fylgiseðill Upplýsingar fylgiseðill búlgarska 13-07-2023
Vara einkenni Vara einkenni búlgarska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla búlgarska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill spænska 13-07-2023
Vara einkenni Vara einkenni spænska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla spænska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill tékkneska 13-07-2023
Vara einkenni Vara einkenni tékkneska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla tékkneska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill danska 13-07-2023
Vara einkenni Vara einkenni danska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla danska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill þýska 13-07-2023
Vara einkenni Vara einkenni þýska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla þýska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill eistneska 13-07-2023
Vara einkenni Vara einkenni eistneska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla eistneska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill gríska 13-07-2023
Vara einkenni Vara einkenni gríska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla gríska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill franska 13-07-2023
Vara einkenni Vara einkenni franska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla franska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill ítalska 13-07-2023
Vara einkenni Vara einkenni ítalska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla ítalska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill lettneska 13-07-2023
Vara einkenni Vara einkenni lettneska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla lettneska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill litháíska 13-07-2023
Vara einkenni Vara einkenni litháíska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla litháíska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill ungverska 13-07-2023
Vara einkenni Vara einkenni ungverska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla ungverska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill maltneska 13-07-2023
Vara einkenni Vara einkenni maltneska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla maltneska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill hollenska 13-07-2023
Vara einkenni Vara einkenni hollenska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla hollenska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill pólska 13-07-2023
Vara einkenni Vara einkenni pólska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla pólska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill portúgalska 13-07-2023
Vara einkenni Vara einkenni portúgalska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla portúgalska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill rúmenska 13-07-2023
Vara einkenni Vara einkenni rúmenska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla rúmenska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill slóvakíska 13-07-2023
Vara einkenni Vara einkenni slóvakíska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla slóvakíska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill slóvenska 13-07-2023
Vara einkenni Vara einkenni slóvenska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla slóvenska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill finnska 13-07-2023
Vara einkenni Vara einkenni finnska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla finnska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill sænska 13-07-2023
Vara einkenni Vara einkenni sænska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla sænska 28-01-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill norska 13-07-2023
Vara einkenni Vara einkenni norska 13-07-2023
Upplýsingar fylgiseðill Upplýsingar fylgiseðill íslenska 13-07-2023
Vara einkenni Vara einkenni íslenska 13-07-2023
Upplýsingar fylgiseðill Upplýsingar fylgiseðill króatíska 13-07-2023
Vara einkenni Vara einkenni króatíska 13-07-2023
Opinber matsskýrsla Opinber matsskýrsla króatíska 28-01-2019

Leitaðu viðvaranir sem tengjast þessari vöru

Skoða skjalasögu