Iblias

Țară: Uniunea Europeană

Limbă: engleză

Sursă: EMA (European Medicines Agency)

Cumpara asta acum

Prospect Prospect (PIL)
27-04-2018

Ingredient activ:

Octocog alfa

Disponibil de la:

Bayer AG

Codul ATC:

B02BD02

INN (nume internaţional):

octocog alfa

Grupul Terapeutică:

Antihemorrhagics

Zonă Terapeutică:

Hemophilia A

Indicații terapeutice:

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

Rezumat produs:

Revision: 4

Statutul autorizaţiei:

Withdrawn

Data de autorizare:

2016-02-18

Prospect

                                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
                                
                                Citiți documentul complet
                                
                            

Caracteristicilor produsului

                                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
                                
                                Citiți documentul complet
                                
                            

Documente în alte limbi

Prospect Prospect bulgară 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului bulgară 27-04-2018
Raport public de evaluare Raport public de evaluare bulgară 09-03-2016
Prospect Prospect spaniolă 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului spaniolă 27-04-2018
Raport public de evaluare Raport public de evaluare spaniolă 09-03-2016
Prospect Prospect cehă 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului cehă 27-04-2018
Raport public de evaluare Raport public de evaluare cehă 09-03-2016
Prospect Prospect daneză 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului daneză 27-04-2018
Raport public de evaluare Raport public de evaluare daneză 09-03-2016
Prospect Prospect germană 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului germană 27-04-2018
Raport public de evaluare Raport public de evaluare germană 09-03-2016
Prospect Prospect estoniană 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului estoniană 27-04-2018
Raport public de evaluare Raport public de evaluare estoniană 09-03-2016
Prospect Prospect greacă 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului greacă 27-04-2018
Raport public de evaluare Raport public de evaluare greacă 09-03-2016
Prospect Prospect franceză 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului franceză 27-04-2018
Raport public de evaluare Raport public de evaluare franceză 09-03-2016
Prospect Prospect italiană 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului italiană 27-04-2018
Raport public de evaluare Raport public de evaluare italiană 09-03-2016
Prospect Prospect letonă 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului letonă 27-04-2018
Raport public de evaluare Raport public de evaluare letonă 09-03-2016
Prospect Prospect lituaniană 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului lituaniană 27-04-2018
Raport public de evaluare Raport public de evaluare lituaniană 09-03-2016
Prospect Prospect maghiară 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului maghiară 27-04-2018
Raport public de evaluare Raport public de evaluare maghiară 09-03-2016
Prospect Prospect malteză 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului malteză 27-04-2018
Raport public de evaluare Raport public de evaluare malteză 09-03-2016
Prospect Prospect olandeză 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului olandeză 27-04-2018
Raport public de evaluare Raport public de evaluare olandeză 09-03-2016
Prospect Prospect poloneză 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului poloneză 27-04-2018
Raport public de evaluare Raport public de evaluare poloneză 09-03-2016
Prospect Prospect portugheză 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului portugheză 27-04-2018
Raport public de evaluare Raport public de evaluare portugheză 09-03-2016
Prospect Prospect română 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului română 27-04-2018
Raport public de evaluare Raport public de evaluare română 09-03-2016
Prospect Prospect slovacă 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului slovacă 27-04-2018
Raport public de evaluare Raport public de evaluare slovacă 09-03-2016
Prospect Prospect slovenă 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului slovenă 27-04-2018
Raport public de evaluare Raport public de evaluare slovenă 09-03-2016
Prospect Prospect finlandeză 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului finlandeză 27-04-2018
Raport public de evaluare Raport public de evaluare finlandeză 09-03-2016
Prospect Prospect suedeză 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului suedeză 27-04-2018
Raport public de evaluare Raport public de evaluare suedeză 09-03-2016
Prospect Prospect norvegiană 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului norvegiană 27-04-2018
Prospect Prospect islandeză 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului islandeză 27-04-2018
Prospect Prospect croată 27-04-2018
Caracteristicilor produsului Caracteristicilor produsului croată 27-04-2018
Raport public de evaluare Raport public de evaluare croată 09-03-2016

Căutați alerte legate de acest produs

Vizualizați istoricul documentelor