Iblias

Riik: Euroopa Liit

keel: inglise

Allikas: EMA (European Medicines Agency)

Osta kohe

Infovoldik Infovoldik (PIL)
27-04-2018
Toote omadused Toote omadused (SPC)
27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande (PAR)
09-03-2016

Toimeaine:

Octocog alfa

Saadav alates:

Bayer AG

ATC kood:

B02BD02

INN (Rahvusvaheline Nimetus):

octocog alfa

Terapeutiline rühm:

Antihemorrhagics

Terapeutiline ala:

Hemophilia A

Näidustused:

Treatment and prophylaxis of bleeding in patients with haemophilia A (congenital factor VIII deficiency).Iblias can be used for all age groups.

Toote kokkuvõte:

Revision: 4

Volitamisolek:

Withdrawn

Loa andmise kuupäev:

2016-02-18

Infovoldik

                                23
B. PACKAGE LEAFLET
24
PACKAGE LEAFLET: INFORMATION FOR THE USER
IBLIAS 250 IU POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
IBLIAS 500 IU POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
IBLIAS 1000 IU POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
IBLIAS 2000 IU POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
IBLIAS 3000 IU POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
Recombinant human coagulation factor VIII (octocog alfa)
This medicine is subject to additional monitoring. This will allow
quick identification of new
safety information. You can help by reporting any side effects you may
get. See the end of section 4
for how to report side effects.
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 Iblias is and what it is used for
2.
What you need to know before you use Iblias
3.
How to use Iblias
4.
Possible side effects
5.
How to store Iblias
6.
Contents of the pack and other information
1.
WHAT IBLIAS IS AND WHAT IT IS USED FOR
Iblias is a medicine that contains the active substance human
recombinant coagulation factor VIII, also
called octocog alfa. Iblias is prepared 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.
Iblias is used for treatment and prevention of bleeding in adults,
adolescents and children of all ages
with haemophilia A (congenital factor VIII deficiency).
2.
WHAT YOU NEED TO KNOW BEFORE YOU USE IBLIAS
DO NOT USE IBLIAS

if you are all
                                
                                Lugege kogu dokumenti
                                
                            

Toote omadused

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
This medicinal product is subject to additional monitoring. This will
allow quick identification of
new safety information. Healthcare professionals are asked to report
any suspected adverse reactions.
See section 4.8 for how to report adverse reactions.
1.
NAME OF THE MEDICINAL PRODUCT
Iblias 250 IU powder and solvent for solution for injection
Iblias 500 IU powder and solvent for solution for injection
Iblias 1000 IU powder and solvent for solution for injection
Iblias 2000 IU powder and solvent for solution for injection
Iblias 3000 IU powder and solvent for solution for injection
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each vial contains nominally 250/500/1000/2000/3000 IU human
coagulation factor VIII.

One mL Iblias 250 IU contains approximately 100 IU (250 IU / 2.5 mL)
of recombinant human
coagulation factor VIII (INN: octocog alfa) after reconstitution with
water for injections.

One mL Iblias 500 IU contains approximately 200 IU (500 IU / 2.5 mL)
of recombinant human
coagulation factor VIII (INN: octocog alfa) after reconstitution with
water for injections.

One mL Iblias 1000 IU contains approximately 400 IU (1000 IU / 2.5 mL)
of recombinant
human coagulation factor VIII (INN: octocog alfa) after reconstitution
with water for injections.

One mL Iblias 2000 IU contains approximately 400 IU (2000 IU / 5 mL)
of recombinant human
coagulation factor VIII (INN: octocog alfa) after reconstitution with
water for injections.

One mL Iblias 3000 IU contains approximately 600 IU (3000 IU / 5 mL)
of recombinant human
coagulation factor VIII (INN: octocog alfa) after reconstitution with
water for injections.
The potency (IU) is determined using the European Pharmacopoeia
chromogenic assay. The specific
activity of Iblias is approximately 4000 IU/mg protein.
Octocog alfa (Full length recombinant human coagulation factor VIII
(rDNA)) is a purified protein
that has 2,332 amino acids. It is produced by recombinant DNA
technology in baby hamster kidney
ce
                                
                                Lugege kogu dokumenti
                                
                            

Dokumendid teistes keeltes

Infovoldik Infovoldik bulgaaria 27-04-2018
Toote omadused Toote omadused bulgaaria 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande bulgaaria 09-03-2016
Infovoldik Infovoldik hispaania 27-04-2018
Toote omadused Toote omadused hispaania 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande hispaania 09-03-2016
Infovoldik Infovoldik tšehhi 27-04-2018
Toote omadused Toote omadused tšehhi 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande tšehhi 09-03-2016
Infovoldik Infovoldik taani 27-04-2018
Toote omadused Toote omadused taani 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande taani 09-03-2016
Infovoldik Infovoldik saksa 27-04-2018
Toote omadused Toote omadused saksa 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande saksa 09-03-2016
Infovoldik Infovoldik eesti 27-04-2018
Toote omadused Toote omadused eesti 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande eesti 09-03-2016
Infovoldik Infovoldik kreeka 27-04-2018
Toote omadused Toote omadused kreeka 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande kreeka 09-03-2016
Infovoldik Infovoldik prantsuse 27-04-2018
Toote omadused Toote omadused prantsuse 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande prantsuse 09-03-2016
Infovoldik Infovoldik itaalia 27-04-2018
Toote omadused Toote omadused itaalia 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande itaalia 09-03-2016
Infovoldik Infovoldik läti 27-04-2018
Toote omadused Toote omadused läti 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande läti 09-03-2016
Infovoldik Infovoldik leedu 27-04-2018
Toote omadused Toote omadused leedu 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande leedu 09-03-2016
Infovoldik Infovoldik ungari 27-04-2018
Toote omadused Toote omadused ungari 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande ungari 09-03-2016
Infovoldik Infovoldik malta 27-04-2018
Toote omadused Toote omadused malta 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande malta 09-03-2016
Infovoldik Infovoldik hollandi 27-04-2018
Toote omadused Toote omadused hollandi 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande hollandi 09-03-2016
Infovoldik Infovoldik poola 27-04-2018
Toote omadused Toote omadused poola 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande poola 09-03-2016
Infovoldik Infovoldik portugali 27-04-2018
Toote omadused Toote omadused portugali 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande portugali 09-03-2016
Infovoldik Infovoldik rumeenia 27-04-2018
Toote omadused Toote omadused rumeenia 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande rumeenia 09-03-2016
Infovoldik Infovoldik slovaki 27-04-2018
Toote omadused Toote omadused slovaki 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande slovaki 09-03-2016
Infovoldik Infovoldik sloveeni 27-04-2018
Toote omadused Toote omadused sloveeni 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande sloveeni 09-03-2016
Infovoldik Infovoldik soome 27-04-2018
Toote omadused Toote omadused soome 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande soome 09-03-2016
Infovoldik Infovoldik rootsi 27-04-2018
Toote omadused Toote omadused rootsi 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande rootsi 09-03-2016
Infovoldik Infovoldik norra 27-04-2018
Toote omadused Toote omadused norra 27-04-2018
Infovoldik Infovoldik islandi 27-04-2018
Toote omadused Toote omadused islandi 27-04-2018
Infovoldik Infovoldik horvaadi 27-04-2018
Toote omadused Toote omadused horvaadi 27-04-2018
Avaliku hindamisaruande Avaliku hindamisaruande horvaadi 09-03-2016

Otsige selle tootega seotud teateid

Vaadake dokumentide ajalugu