Accofil

Land: Europäische Union

Sprache: Englisch

Quelle: EMA (European Medicines Agency)

Kaufe es jetzt

Wirkstoff:

filgrastim

Verfügbar ab:

Accord Healthcare S.L.U.

ATC-Code:

L03AA02

INN (Internationale Bezeichnung):

filgrastim

Therapiegruppe:

Immunostimulants,

Therapiebereich:

Neutropenia

Anwendungsgebiete:

Accofil is indicated for the reduction in the duration of neutropenia and the incidence of febrile neutropenia in patients treated with established cytotoxic chemotherapy for malignancy (with the exception of chronic myeloid leukaemia and myelodysplastic syndromes) and for the reduction in the duration of neutropenia in patients undergoing myeloablative therapy followed by bone marrow transplantation considered to be at increased risk of prolonged severe neutropenia. The safety and efficacy of Accofil are similar in adults and children receiving cytotoxic chemotherapy.Accofil is indicated for the mobilisation of peripheral blood progenitor cells (PBPCs).In patients, children or adults with severe congenital, cyclic, or idiopathic neutropenia with an absolute neutrophil count (ANC) of ≤ 0.5 x 109/L, and a history of severe or recurrent infections, long term administration of Accofil is indicated to increase neutrophil counts and to reduce the incidence and duration of infection-related events.Accofil is indicated for the treatment of persistent neutropenia (ANC less than or equal to 1.0 x 109/L) in patients with advanced HIV infection, in order to reduce the risk of bacterial infections when other options to manage neutropenia are inappropriate.

Produktbesonderheiten:

Revision: 14

Berechtigungsstatus:

Authorised

Berechtigungsdatum:

2014-09-17

Gebrauchsinformation

                                102
B. PACKAGE LEAFLET
103
PACKAGE LEAFLET: INFORMATION FOR THE USER
_ _
ACCOFIL 30 MU/0.5 ML (0.6 MG/ML) SOLUTION FOR INJECTION/INFUSION IN
PRE-FILLED SYRINGE
filgrastim
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, nurse 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, pharmacist or nurse.
This includes any possible
side effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Accofil is and what it is used for
2.
What you need to know before you use Accofil
3.
How to use Accofil
4.
Possible side effects
5. How to store Accofil
6. Contents of the pack and other information
1.
WHAT ACCOFIL IS AND WHAT IT IS USED FOR
WHAT ACCOFIL IS
Accofil is a white blood cell growth factor (granulocyte-colony
stimulating factor) and belong to a
group of medicines called cytokines. Growth factors are proteins that
are produced naturally in the
body but they can also be made using biotechnology for use as a
medicine. Accofil works by
encouraging the bone marrow to produce more white blood cells.
A reduction in the number of white blood cells (neutropenia) can occur
for several reasons and makes
your body less able to fight infection. Accofil stimulates the bone
marrow to produce new white cells
quickly.
Accofil can be used:
-
to increase the number of white blood cells after treatment with
chemotherapy to help prevent
infections;
-
to increase the number of white blood cells after a bone marrow
transplant to help prevent
infections;
-
before high-dose chemotherapy to make the bone marrow produce more
stem cells which can
be collected and given back to you after your treatment. These can be
taken from you or from
a donor. The stem cells will then go b
                                
                                Lesen Sie das vollständige Dokument
                                
                            

Fachinformation

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Accofil 30 MU/0.5 ml solution for injection/infusion in pre-filled
syringe
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each pre-filled syringe contains 30 million units (MU)/300 micrograms
of filgrastim in 0.5 ml
(0.6 mg/ml) solution for injection or infusion.
Filgrastim is a recombinant methionyl human granulocyte-colony
stimulating factor produced in
_Escherichia coli _
(BL21) by recombinant DNA technology.
Excipient with known effect:
Each ml of solution contains 50 mg of sorbitol (E420).
_ _
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Solution for injection in pre-filled syringe
Concentrate for solution for infusion in pre-filled syringe
Clear, colourless solution.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Accofil is indicated for the reduction in the duration of neutropenia
and the incidence of febrile
neutropenia in patients treated with established cytotoxic
chemotherapy for malignancy (with the
exception of chronic myeloid leukaemia and myelodysplastic syndromes)
and for the reduction in the
duration of neutropenia in patients undergoing myeloablative therapy
followed by bone marrow
transplantation considered to be at increased risk of prolonged severe
neutropenia.
The safety and
efficacy of Accofil are similar in adults and children receiving
cytotoxic chemotherapy.
Accofil is indicated for the mobilisation of peripheral blood
progenitor cells (PBPCs).
In patients, children or adults with severe congenital, cyclic, or
idiopathic neutropenia with an absolute
neutrophil count (ANC) of ≤ 0.5 x 10
9
/L, and a history of severe or recurrent infections, long term
administration of Accofil is indicated to increase neutrophil counts
and to reduce the incidence and
duration of infection-related events.
Accofil is indicated f
or the treatment of persistent neutropenia (ANC less than or equal to
1.0 x
10
9
/L)
in patients with advanced HIV infection, in order to reduce the risk
of bacterial infec
                                
                                Lesen Sie das vollständige Dokument
                                
                            

Dokumente in anderen Sprachen

Gebrauchsinformation Gebrauchsinformation Bulgarisch 15-03-2024
Fachinformation Fachinformation Bulgarisch 15-03-2024
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Bulgarisch 28-10-2014
Gebrauchsinformation Gebrauchsinformation Spanisch 15-03-2024
Fachinformation Fachinformation Spanisch 15-03-2024
Gebrauchsinformation Gebrauchsinformation Tschechisch 15-03-2024
Fachinformation Fachinformation Tschechisch 15-03-2024
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Tschechisch 28-10-2014
Gebrauchsinformation Gebrauchsinformation Dänisch 15-03-2024
Fachinformation Fachinformation Dänisch 15-03-2024
Gebrauchsinformation Gebrauchsinformation Deutsch 15-03-2024
Fachinformation Fachinformation Deutsch 15-03-2024
Gebrauchsinformation Gebrauchsinformation Estnisch 15-03-2024
Fachinformation Fachinformation Estnisch 15-03-2024
Gebrauchsinformation Gebrauchsinformation Griechisch 15-03-2024
Fachinformation Fachinformation Griechisch 15-03-2024
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Griechisch 28-10-2014
Gebrauchsinformation Gebrauchsinformation Französisch 15-03-2024
Fachinformation Fachinformation Französisch 15-03-2024
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Französisch 28-10-2014
Gebrauchsinformation Gebrauchsinformation Italienisch 15-03-2024
Fachinformation Fachinformation Italienisch 15-03-2024
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Italienisch 28-10-2014
Gebrauchsinformation Gebrauchsinformation Lettisch 15-03-2024
Fachinformation Fachinformation Lettisch 15-03-2024
Gebrauchsinformation Gebrauchsinformation Litauisch 15-03-2024
Fachinformation Fachinformation Litauisch 15-03-2024
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Litauisch 28-10-2014
Gebrauchsinformation Gebrauchsinformation Ungarisch 15-03-2024
Fachinformation Fachinformation Ungarisch 15-03-2024
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Ungarisch 28-10-2014
Gebrauchsinformation Gebrauchsinformation Maltesisch 15-03-2024
Fachinformation Fachinformation Maltesisch 15-03-2024
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Maltesisch 28-10-2014
Gebrauchsinformation Gebrauchsinformation Niederländisch 15-03-2024
Fachinformation Fachinformation Niederländisch 15-03-2024
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Niederländisch 28-10-2014
Gebrauchsinformation Gebrauchsinformation Polnisch 15-03-2024
Fachinformation Fachinformation Polnisch 15-03-2024
Gebrauchsinformation Gebrauchsinformation Portugiesisch 15-03-2024
Fachinformation Fachinformation Portugiesisch 15-03-2024
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Portugiesisch 28-10-2014
Gebrauchsinformation Gebrauchsinformation Rumänisch 15-03-2024
Fachinformation Fachinformation Rumänisch 15-03-2024
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Rumänisch 28-10-2014
Gebrauchsinformation Gebrauchsinformation Slowakisch 15-03-2024
Fachinformation Fachinformation Slowakisch 15-03-2024
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Slowakisch 28-10-2014
Gebrauchsinformation Gebrauchsinformation Slowenisch 15-03-2024
Fachinformation Fachinformation Slowenisch 15-03-2024
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Slowenisch 28-10-2014
Gebrauchsinformation Gebrauchsinformation Finnisch 15-03-2024
Fachinformation Fachinformation Finnisch 15-03-2024
Gebrauchsinformation Gebrauchsinformation Schwedisch 15-03-2024
Fachinformation Fachinformation Schwedisch 15-03-2024
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Schwedisch 28-10-2014
Gebrauchsinformation Gebrauchsinformation Norwegisch 15-03-2024
Fachinformation Fachinformation Norwegisch 15-03-2024
Gebrauchsinformation Gebrauchsinformation Isländisch 15-03-2024
Fachinformation Fachinformation Isländisch 15-03-2024
Gebrauchsinformation Gebrauchsinformation Kroatisch 15-03-2024
Fachinformation Fachinformation Kroatisch 15-03-2024
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Kroatisch 28-10-2014

Suchen Sie nach Benachrichtigungen zu diesem Produkt

Dokumentverlauf anzeigen