ReFacto AF

Pays: Union européenne

Langue: anglais

Source: EMA (European Medicines Agency)

Achète-le

Ingrédients actifs:

moroctocog alfa

Disponible depuis:

Pfizer Europe MA EEIG

Code ATC:

B02BD02

DCI (Dénomination commune internationale):

moroctocog alfa

Groupe thérapeutique:

Antihemorrhagics

Domaine thérapeutique:

Hemophilia A

indications thérapeutiques:

Treatment and prophylaxis of bleeding in patients with haemophilia A (congenital factor-VIII deficiency). ReFacto AF is appropriate for use in adults and children of all ages, including newborns. ReFacto AF does not contain von-Willebrand factor, and hence is not indicated in von-Willebrand's disease.,

Descriptif du produit:

Revision: 40

Statut de autorisation:

Authorised

Date de l'autorisation:

1999-04-13

Notice patient

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
ReFacto AF 250 IU powder and solvent for solution for injection
ReFacto AF 500 IU powder and solvent for solution for injection
ReFacto AF 1000 IU powder and solvent for solution for injection
ReFacto AF 2000 IU powder and solvent for solution for injection
ReFacto AF 250 IU powder and solvent for solution for injection in
pre-filled syringe
ReFacto AF 500 IU powder and solvent for solution for injection in
pre-filled syringe
ReFacto AF 1000 IU powder and solvent for solution for injection in
pre-filled syringe
ReFacto AF 2000 IU powder and solvent for solution for injection in
pre-filled syringe
ReFacto AF 3000 IU powder and solvent for solution for injection in
pre-filled syringe
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
ReFacto AF 250 IU powder and solvent for solution for injection
Each vial contains nominally 250 IU* moroctocog alfa**.
After reconstitution, each mL of solution contains approximately 62.5
IU moroctocog alfa.
ReFacto AF 500 IU powder and solvent for solution for injection
Each vial contains nominally 500 IU* moroctocog alfa**.
After reconstitution, each mL of solution contains approximately 125
IU moroctocog alfa.
ReFacto AF 1000 IU powder and solvent for solution for injection
Each vial contains nominally 1000 IU* moroctocog alfa**.
After reconstitution, each mL of solution contains approximately 250
IU moroctocog alfa.
ReFacto AF 2000 IU powder and solvent for solution for injection
Each vial contains nominally 2000 IU* moroctocog alfa**.
After reconstitution, each mL of solution contains approximately 500
IU moroctocog alfa.
ReFacto AF 250 IU powder and solvent for solution for injection in
pre-filled syringe
Each pre-filled syringe contains nominally 250 IU* moroctocog alfa**.
After reconstitution, each mL of solution contains approximately 62.5
IU moroctocog alfa.
ReFacto AF 500 IU powder and solvent for solution for injection in
pre-filled syringe
Each pre-filled syringe contains nominally 500 IU* moroctoco
                                
                                Lire le document complet
                                
                            

Résumé des caractéristiques du produit

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
ReFacto AF 250 IU powder and solvent for solution for injection
ReFacto AF 500 IU powder and solvent for solution for injection
ReFacto AF 1000 IU powder and solvent for solution for injection
ReFacto AF 2000 IU powder and solvent for solution for injection
ReFacto AF 250 IU powder and solvent for solution for injection in
pre-filled syringe
ReFacto AF 500 IU powder and solvent for solution for injection in
pre-filled syringe
ReFacto AF 1000 IU powder and solvent for solution for injection in
pre-filled syringe
ReFacto AF 2000 IU powder and solvent for solution for injection in
pre-filled syringe
ReFacto AF 3000 IU powder and solvent for solution for injection in
pre-filled syringe
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
ReFacto AF 250 IU powder and solvent for solution for injection
Each vial contains nominally 250 IU* moroctocog alfa**.
After reconstitution, each mL of solution contains approximately 62.5
IU moroctocog alfa.
ReFacto AF 500 IU powder and solvent for solution for injection
Each vial contains nominally 500 IU* moroctocog alfa**.
After reconstitution, each mL of solution contains approximately 125
IU moroctocog alfa.
ReFacto AF 1000 IU powder and solvent for solution for injection
Each vial contains nominally 1000 IU* moroctocog alfa**.
After reconstitution, each mL of solution contains approximately 250
IU moroctocog alfa.
ReFacto AF 2000 IU powder and solvent for solution for injection
Each vial contains nominally 2000 IU* moroctocog alfa**.
After reconstitution, each mL of solution contains approximately 500
IU moroctocog alfa.
ReFacto AF 250 IU powder and solvent for solution for injection in
pre-filled syringe
Each pre-filled syringe contains nominally 250 IU* moroctocog alfa**.
After reconstitution, each mL of solution contains approximately 62.5
IU moroctocog alfa.
ReFacto AF 500 IU powder and solvent for solution for injection in
pre-filled syringe
Each pre-filled syringe contains nominally 500 IU* moroctoco
                                
                                Lire le document complet
                                
                            

Documents dans d'autres langues

Notice patient Notice patient bulgare 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation bulgare 29-09-2016
Notice patient Notice patient espagnol 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation espagnol 29-09-2016
Notice patient Notice patient tchèque 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation tchèque 29-09-2016
Notice patient Notice patient danois 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation danois 29-09-2016
Notice patient Notice patient allemand 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation allemand 29-09-2016
Notice patient Notice patient estonien 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation estonien 29-09-2016
Notice patient Notice patient grec 08-11-2022
Notice patient Notice patient français 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation français 29-09-2016
Notice patient Notice patient italien 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation italien 29-09-2016
Notice patient Notice patient letton 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation letton 29-09-2016
Notice patient Notice patient lituanien 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation lituanien 29-09-2016
Notice patient Notice patient hongrois 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation hongrois 29-09-2016
Notice patient Notice patient maltais 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation maltais 29-09-2016
Notice patient Notice patient néerlandais 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation néerlandais 29-09-2016
Notice patient Notice patient polonais 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation polonais 29-09-2016
Notice patient Notice patient portugais 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation portugais 29-09-2016
Notice patient Notice patient roumain 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation roumain 29-09-2016
Notice patient Notice patient slovaque 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation slovaque 29-09-2016
Notice patient Notice patient slovène 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation slovène 29-09-2016
Notice patient Notice patient finnois 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation finnois 29-09-2016
Notice patient Notice patient suédois 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation suédois 29-09-2016
Notice patient Notice patient norvégien 08-11-2022
Notice patient Notice patient islandais 08-11-2022
Notice patient Notice patient croate 08-11-2022
Rapport public d'évaluation Rapport public d'évaluation croate 29-09-2016

Rechercher des alertes liées à ce produit

Afficher l'historique des documents