NovoSeven

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

eptacog alfa (activated)

Available from:

Novo Nordisk A/S

ATC code:

B02BD08

INN (International Name):

eptacog alfa (activated)

Therapeutic group:

Antihemorrhagics

Therapeutic area:

Hemophilia B; Thrombasthenia; Factor VII Deficiency; Hemophilia A

Therapeutic indications:

NovoSeven is indicated for the treatment of bleeding episodes and for the prevention of bleeding in those undergoing surgery or invasive procedures in the following patient groups:in patients with congenital haemophilia with inhibitors to coagulation factors VIII or IX > 5 Bethesda units (BU);in patients with congenital haemophilia who are expected to have a high anamnestic response to factor-VIII or factor-IX administration;in patients with acquired haemophilia;in patients with congenital factor-VII deficiency;in patients with Glanzmann's thrombasthenia with antibodies to platelet glycoprotein (GP) IIb-IIIa and / or human leucocyte antigens (HLA), and with past or present refractoriness to platelet transfusions.in patients with Glanzmann’s thrombasthenia with past or present refractoriness to platelet transfusions, or where platelets are not readily available. 

Product summary:

Revision: 38

Authorization status:

Authorised

Authorization date:

1996-02-23

Patient Information leaflet

                                37
B. PACKAGE LEAFLET
38
PACKAGE LEAFLET: INFORMATION FOR THE USER
NOVOSEVEN 1 MG (50 KIU) POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
NOVOSEVEN 2 MG (100 KIU) POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
NOVOSEVEN 5 MG (250 KIU) POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
NOVOSEVEN 8 MG (400 KIU) POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
eptacog alfa (activated)
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU ARE GIVEN THIS INJECTION
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.
•
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. This includes any
possible side effects not listed
in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What NovoSeven is and what it is used for
2.
What you need to know before you use NovoSeven
3.
How to use NovoSeven
4.
Possible side effects
5.
How to store NovoSeven
6.
Contents of the pack and other information
Overleaf: Instructions on how to use NovoSeven
1.
WHAT NOVOSEVEN IS AND WHAT IT IS USED FOR
NovoSeven is a blood coagulation factor. It works by making the blood
clot at the site of bleeding,
when the body's own clotting factors are not working.
NovoSeven is used
to treat bleeding, and to prevent excessive bleeding after surgery or
other
important treatments. Early treatment with NovoSeven reduces how much
you bleed and for how long.
It works in all types of bleeds, including joint bleeds. This reduces
the need for hospitalisation and
days absent from work and school.
It is used in certain groups of people:
•
If you were
_born with haemophilia_
and do not respond normally to factors VIII or IX treatment
•
If you have
_acquired haemophilia_
•
If you have
_Factor VII deficiency_
•
If you have
_Glanzmann’s thrombasthenia_
(a bleeding disorder) and your condition cannot be
treated effectively
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
NovoSeven 1 mg (50 KIU) powder and solvent for solution for injection
NovoSeven 2 mg (100 KIU) powder and solvent for solution for injection
NovoSeven 5 mg (250 KIU) powder and solvent for solution for injection
NovoSeven 8 mg (400 KIU) powder and solvent for solution for injection
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
NovoSeven 1 m
g (50 KIU)
NovoSeven is presented as powder and solvent for solution for
injection containing 1 mg eptacog alfa
(activated) per vial (corresponds to 50 KIU/vial).
NovoSeven 2 m
g (100 KIU)
NovoSeven is presented as powder and solvent for solution for
injection containing 2 mg eptacog alfa
(activated) per vial (corresponds to 100 KIU/vial).
NovoSeven 5 m
g (250 KIU)
NovoSeven is presented as powder and solvent for solution for
injection containing 5 mg eptacog alfa
(activated) per vial (corresponds to 250 KIU/vial).
NovoSeven 8 mg (400 KIU)
NovoSeven is presented as powder and solvent for solution for
injection containing 8 mg eptacog alfa
(activated) per vial (corresponds to 400 KIU/vial).
1 KIU equals 1,000 IU (International Units).
eptacog alfa (activated) is recombinant coagulation factor VIIa
(rFVIIa) with a molecular mass of
approximately 50,000 Daltons produced in baby hamster kidney cells
(BHK Cells) by recombinant
DNA technology.
After reconstitution, the product contains 1 mg/ml eptacog alfa
(activated) when reconstituted with
solvent.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Powder and solvent for solution for injection.
White lyophilised powder. Solvent: clear colourless solution. The
reconstituted solution has a pH of
approximately 6.0.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
NovoSeven is indicated for the treatment of bleeding episodes and for
the prevention of bleeding in
those undergoing surgery or invasive procedures in the following
patient groups:
•
in patients with congenital haemophilia with inhibitors to coagulation
factors VIII or
IX
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 05-01-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 05-01-2023
Public Assessment Report Public Assessment Report Bulgarian 26-07-2022
Patient Information leaflet Patient Information leaflet Spanish 05-01-2023
Public Assessment Report Public Assessment Report Spanish 26-07-2022
Patient Information leaflet Patient Information leaflet Czech 05-01-2023
Public Assessment Report Public Assessment Report Czech 26-07-2022
Patient Information leaflet Patient Information leaflet Danish 05-01-2023
Public Assessment Report Public Assessment Report Danish 26-07-2022
Patient Information leaflet Patient Information leaflet German 05-01-2023
Public Assessment Report Public Assessment Report German 26-07-2022
Patient Information leaflet Patient Information leaflet Estonian 05-01-2023
Public Assessment Report Public Assessment Report Estonian 26-07-2022
Patient Information leaflet Patient Information leaflet Greek 05-01-2023
Public Assessment Report Public Assessment Report Greek 26-07-2022
Patient Information leaflet Patient Information leaflet French 05-01-2023
Public Assessment Report Public Assessment Report French 26-07-2022
Patient Information leaflet Patient Information leaflet Italian 05-01-2023
Public Assessment Report Public Assessment Report Italian 26-07-2022
Patient Information leaflet Patient Information leaflet Latvian 05-01-2023
Public Assessment Report Public Assessment Report Latvian 26-07-2022
Patient Information leaflet Patient Information leaflet Lithuanian 05-01-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 05-01-2023
Public Assessment Report Public Assessment Report Lithuanian 26-07-2022
Patient Information leaflet Patient Information leaflet Hungarian 05-01-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 05-01-2023
Public Assessment Report Public Assessment Report Hungarian 26-07-2022
Patient Information leaflet Patient Information leaflet Maltese 05-01-2023
Public Assessment Report Public Assessment Report Maltese 26-07-2022
Patient Information leaflet Patient Information leaflet Dutch 05-01-2023
Public Assessment Report Public Assessment Report Dutch 26-07-2022
Patient Information leaflet Patient Information leaflet Polish 05-01-2023
Public Assessment Report Public Assessment Report Polish 26-07-2022
Patient Information leaflet Patient Information leaflet Portuguese 05-01-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 05-01-2023
Public Assessment Report Public Assessment Report Portuguese 26-07-2022
Patient Information leaflet Patient Information leaflet Romanian 05-01-2023
Public Assessment Report Public Assessment Report Romanian 26-07-2022
Patient Information leaflet Patient Information leaflet Slovak 05-01-2023
Public Assessment Report Public Assessment Report Slovak 26-07-2022
Patient Information leaflet Patient Information leaflet Slovenian 05-01-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 05-01-2023
Public Assessment Report Public Assessment Report Slovenian 26-07-2022
Patient Information leaflet Patient Information leaflet Finnish 05-01-2023
Public Assessment Report Public Assessment Report Finnish 26-07-2022
Patient Information leaflet Patient Information leaflet Swedish 05-01-2023
Public Assessment Report Public Assessment Report Swedish 26-07-2022
Patient Information leaflet Patient Information leaflet Norwegian 05-01-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 05-01-2023
Patient Information leaflet Patient Information leaflet Icelandic 05-01-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 05-01-2023
Patient Information leaflet Patient Information leaflet Croatian 05-01-2023
Public Assessment Report Public Assessment Report Croatian 26-07-2022

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