BeneFIX

Riik: Euroopa Liit

keel: inglise

Allikas: EMA (European Medicines Agency)

Osta kohe

Infovoldik Infovoldik (PIL)
17-10-2022
Toote omadused Toote omadused (SPC)
17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande (PAR)
30-10-2015

Toimeaine:

Nonacog alfa

Saadav alates:

Pfizer Europe MA EEIG

ATC kood:

B02BD04

INN (Rahvusvaheline Nimetus):

nonacog alfa

Terapeutiline rühm:

Antihemorrhagics

Terapeutiline ala:

Hemophilia B

Näidustused:

Treatment and prophylaxis of bleeding in patients with haemophilia B (congenital factor-IX deficiency).,

Toote kokkuvõte:

Revision: 42

Volitamisolek:

Authorised

Loa andmise kuupäev:

1997-08-27

Infovoldik

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
BeneFIX 250 IU powder and solvent for solution for injection
BeneFIX 500 IU powder and solvent for solution for injection
BeneFIX 1000 IU powder and solvent for solution for injection
BeneFIX 1500 IU powder and solvent for solution for injection
BeneFIX 2000 IU powder and solvent for solution for injection
BeneFIX 3000 IU powder and solvent for solution for injection
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
BeneFIX 250 IU powder and solvent for solution for injection
Each vial contains nominally 250 IU nonacog alfa (recombinant
coagulation factor IX). After
reconstitution with the accompanying 5 mL (0.234%) sodium chloride
solution for injection, each mL
of the solution contains approximately 50 IU nonacog alfa.
BeneFIX 500 IU powder and solvent for solution for injection
Each vial contains nominally 500 IU nonacog alfa (recombinant
coagulation factor IX). After
reconstitution with the accompanying 5 mL (0.234%) sodium chloride
solution for injection, each mL
of the solution contains approximately 100 IU nonacog alfa.
BeneFIX 1000 IU powder and solvent for solution for injection
Each vial contains nominally 1000 IU nonacog alfa (recombinant
coagulation factor IX). After
reconstitution with the accompanying 5 mL (0.234%) sodium chloride
solution for injection, each mL
of the solution contains approximately 200 IU nonacog alfa.
BeneFIX 1500 IU powder and solvent for solution for injection
Each vial contains nominally 1500 IU nonacog alfa (recombinant
coagulation factor IX). After
reconstitution with the accompanying 5 mL (0.234%) sodium chloride
solution for injection, each mL
of the solution contains approximately 300 IU nonacog alfa.
BeneFIX 2000 IU powder and solvent for solution for injection
Each vial contains nominally 2000 IU nonacog alfa (recombinant
coagulation factor IX). After
reconstitution with the accompanying 5 mL (0.234%) sodium chloride
solution for injection, each mL
of the solution contains approximately 400 IU non
                                
                                Lugege kogu dokumenti
                                
                            

Toote omadused

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
BeneFIX 250 IU powder and solvent for solution for injection
BeneFIX 500 IU powder and solvent for solution for injection
BeneFIX 1000 IU powder and solvent for solution for injection
BeneFIX 1500 IU powder and solvent for solution for injection
BeneFIX 2000 IU powder and solvent for solution for injection
BeneFIX 3000 IU powder and solvent for solution for injection
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
BeneFIX 250 IU powder and solvent for solution for injection
Each vial contains nominally 250 IU nonacog alfa (recombinant
coagulation factor IX). After
reconstitution with the accompanying 5 mL (0.234%) sodium chloride
solution for injection, each mL
of the solution contains approximately 50 IU nonacog alfa.
BeneFIX 500 IU powder and solvent for solution for injection
Each vial contains nominally 500 IU nonacog alfa (recombinant
coagulation factor IX). After
reconstitution with the accompanying 5 mL (0.234%) sodium chloride
solution for injection, each mL
of the solution contains approximately 100 IU nonacog alfa.
BeneFIX 1000 IU powder and solvent for solution for injection
Each vial contains nominally 1000 IU nonacog alfa (recombinant
coagulation factor IX). After
reconstitution with the accompanying 5 mL (0.234%) sodium chloride
solution for injection, each mL
of the solution contains approximately 200 IU nonacog alfa.
BeneFIX 1500 IU powder and solvent for solution for injection
Each vial contains nominally 1500 IU nonacog alfa (recombinant
coagulation factor IX). After
reconstitution with the accompanying 5 mL (0.234%) sodium chloride
solution for injection, each mL
of the solution contains approximately 300 IU nonacog alfa.
BeneFIX 2000 IU powder and solvent for solution for injection
Each vial contains nominally 2000 IU nonacog alfa (recombinant
coagulation factor IX). After
reconstitution with the accompanying 5 mL (0.234%) sodium chloride
solution for injection, each mL
of the solution contains approximately 400 IU non
                                
                                Lugege kogu dokumenti
                                
                            

Dokumendid teistes keeltes

Infovoldik Infovoldik bulgaaria 17-10-2022
Toote omadused Toote omadused bulgaaria 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande bulgaaria 30-10-2015
Infovoldik Infovoldik hispaania 17-10-2022
Toote omadused Toote omadused hispaania 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande hispaania 30-10-2015
Infovoldik Infovoldik tšehhi 17-10-2022
Toote omadused Toote omadused tšehhi 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande tšehhi 30-10-2015
Infovoldik Infovoldik taani 17-10-2022
Toote omadused Toote omadused taani 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande taani 30-10-2015
Infovoldik Infovoldik saksa 17-10-2022
Toote omadused Toote omadused saksa 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande saksa 30-10-2015
Infovoldik Infovoldik eesti 17-10-2022
Toote omadused Toote omadused eesti 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande eesti 30-10-2015
Infovoldik Infovoldik kreeka 17-10-2022
Toote omadused Toote omadused kreeka 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande kreeka 30-10-2015
Infovoldik Infovoldik prantsuse 17-10-2022
Toote omadused Toote omadused prantsuse 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande prantsuse 30-10-2015
Infovoldik Infovoldik itaalia 17-10-2022
Toote omadused Toote omadused itaalia 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande itaalia 30-10-2015
Infovoldik Infovoldik läti 17-10-2022
Toote omadused Toote omadused läti 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande läti 30-10-2015
Infovoldik Infovoldik leedu 17-10-2022
Toote omadused Toote omadused leedu 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande leedu 30-10-2015
Infovoldik Infovoldik ungari 17-10-2022
Toote omadused Toote omadused ungari 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande ungari 30-10-2015
Infovoldik Infovoldik malta 17-10-2022
Toote omadused Toote omadused malta 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande malta 30-10-2015
Infovoldik Infovoldik hollandi 17-10-2022
Toote omadused Toote omadused hollandi 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande hollandi 30-10-2015
Infovoldik Infovoldik poola 17-10-2022
Toote omadused Toote omadused poola 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande poola 30-10-2015
Infovoldik Infovoldik portugali 17-10-2022
Toote omadused Toote omadused portugali 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande portugali 30-10-2015
Infovoldik Infovoldik rumeenia 17-10-2022
Toote omadused Toote omadused rumeenia 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande rumeenia 30-10-2015
Infovoldik Infovoldik slovaki 17-10-2022
Toote omadused Toote omadused slovaki 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande slovaki 30-10-2015
Infovoldik Infovoldik sloveeni 17-10-2022
Toote omadused Toote omadused sloveeni 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande sloveeni 30-10-2015
Infovoldik Infovoldik soome 17-10-2022
Toote omadused Toote omadused soome 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande soome 30-10-2015
Infovoldik Infovoldik rootsi 17-10-2022
Toote omadused Toote omadused rootsi 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande rootsi 30-10-2015
Infovoldik Infovoldik norra 17-10-2022
Toote omadused Toote omadused norra 17-10-2022
Infovoldik Infovoldik islandi 17-10-2022
Toote omadused Toote omadused islandi 17-10-2022
Infovoldik Infovoldik horvaadi 17-10-2022
Toote omadused Toote omadused horvaadi 17-10-2022
Avaliku hindamisaruande Avaliku hindamisaruande horvaadi 30-10-2015

Otsige selle tootega seotud teateid

Vaadake dokumentide ajalugu