Alexan

Država: Armenija

Jezik: engleski

Izvor: Դեղերի և բժշկական տեխնոլոգիաների փորձագիտական կենտրոնի գործունեության Հայաստանի Հանրապետությունում

Preuzimanje Svojstava lijeka (SPC)
14-05-2018

Aktivni sastojci:

cytarabine

Dostupno od:

EBEWE Pharma Ges. m.b.H. Nfg. KG

INN (International ime):

cytarabine

Doziranje:

50mg/ml

Farmaceutski oblik:

solution for injection

Tip recepta:

Prescription

Svojstava lijeka

                                m12 - en-spc-pl-w - 3
1
PRESCRIBING INFORMATION
1.
NAME OF THE MEDICINAL PRODUCT
Alexan
®
Solution for injection and infusion
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Alexan
®
100 mg: One vial with 5 ml solution contains 100 mg cytarabine (20
mg/ml).
Alexan
®
500 mg: One vial with 10 ml solution contains 500 mg cytarabine (50
mg/ml).
Alexan
®
1000 mg: One vial with 20 ml solution contains 1000 mg cytarabine (50
mg/ml).
For the list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Solution for injection and infusion
Clear and colourless solution
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Alexan is used in adults.
1. Standard treatment:
Cytarabine is a cytostatic drug for the induction therapy of a
clinical remission and/or
maintenance therapy in patients with:

acute non-lymphoblast leukaemia,

acute lymphoblast leukaemia,

acute myeloid leukaemia,

diffuse hystiocytic lymphoma (non-Hodgkin’s lymphoma with high level
of
malignancy).
2. High dose cytarabine therapy is indicated in patients with:

refractory acute non-lymphoblast leukaemia,

refractory acute lymphoblast leukaemia,

blast crisis in chronic myeloid leukaemia,

leukaemias with particular risk, e.g. acute leukaemias with secondary
carcinoma
after previous chemotherapy and/or irradiation,

refractory non-Hodgkin’s lymphomas.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
POSOLOGY
The treatment with Alexan should be initiated under the monitoring or
consultation of a
physician with experience in treatment with cytostatics.
m12 - en-spc-pl-w - 3
2
It must be assumed that effective cytarabine plasma levels are between
0.01 and
0.15

g/ml. The dose must be determined exactly and individually, preferably
according to
body surface area (BSA).
Cytarabine is used in combination with other cytostatic substances
within complex therapy
protocols.
Only general dosing recommendations can be given. For exact dosing,
see treatment
protocols in the specialised literature.
Patients with hepatic or renal impairment
In pat
                                
                                Pročitajte cijeli dokument
                                
                            

Dokumenti na drugim jezicima

Uputa o lijeku Uputa o lijeku ruski 14-05-2018

Upozorenja za pretraživanje vezana za ovaj proizvod

Pogledajte povijest dokumenata