BENEFIX POWDER FOR SOLUTION

Šalis: Kanada

kalba: anglų

Šaltinis: Health Canada

Nusipirk tai dabar

Parsisiųsti Prekės savybės (SPC)
21-07-2017

Veiklioji medžiaga:

COAGULATION FACTOR IX (RECOMBINANT)

Prieinama:

PFIZER CANADA ULC

ATC kodas:

B02BD04

INN (Tarptautinis Pavadinimas):

COAGULATION FACTOR IX

Dozė:

3000UNIT

Vaisto forma:

POWDER FOR SOLUTION

Sudėtis:

COAGULATION FACTOR IX (RECOMBINANT) 3000UNIT

Vartojimo būdas:

INTRAVENOUS

Vienetai pakuotėje:

15G/50G

Recepto tipas:

Schedule D

Gydymo sritis:

HEMOSTATICS

Produkto santrauka:

Active ingredient group (AIG) number: 0152202005; AHFS:

Autorizacija statusas:

APPROVED

Leidimo data:

2012-09-05

Prekės savybės

                                _ _
_BeneFIX_
_®_
_ (coagulation factor IX) Product Monograph _
_Page 1 of 30 _
PRODUCT MONOGRAPH
BENEFIX
®
COAGULATION FACTOR IX (RECOMBINANT)
INN= NONACOG ALFA
BENEFIX
 COAGULATION FACTOR IX (RECOMBINANT), IS PREPARED IN SIX LYOPHILIZED
POWDER DOSAGE FORMS NOMINALLY CONTAINING 250, 500, 1000, 1500, 2000
AND
3000 IU PER VIAL. THE RECONSTITUTED PRODUCT CONTAINS APPROXIMATELY:
50, 100,
200, 300, 400 AND 600 IU/ML, RESPECTIVELY.
WORLD HEALTH ORGANIZATION (WHO) INTERNATIONAL STANDARD FOR FACTOR IX
CONCENTRATE
ANTIHEMORRHAGIC BLOOD COAGULATION FACTOR IX
®
T.M. GENETICS INSTITUTE LLC
PFIZER CANADA INC., LICENSEE
17,300 TRANS-CANADA HIGHWAY
KIRKLAND, QUEBEC H9J 2M5
SUBMISSION CONTROL NO: 200822 DATE OF APPROVAL: JULY 21, 2017
©
PFIZER CANADA INC.
_ _
_BeneFIX_
_®_
_ (coagulation factor IX) Product Monograph _
_Page 2 of 30 _
_ _
_BeneFIX_
_®_
_ (coagulation factor IX) Product Monograph _
_Page 3 of 30 _
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
......................................................... 4
SUMMARY PRODUCT INFORMATION
.............................................................................
4
INDICATIONS AND CLINICAL USE
...................................................................................
4
CONTRAINDICATIONS..........................................................................................................
5
WARNINGS AND PRECAUTIONS
........................................................................................
5
ADVERSE REACTIONS
..........................................................................................................
8
DRUG INTERACTIONS
........................................................................................................
10
DOSAGE AND ADMINISTRATION
....................................................................................
10
OVERDOSAGE
........................................................................................................................
14
ACTION AND CLINICAL
PHARMACOLOGY...........
                                
                                Perskaitykite visą dokumentą
                                
                            

Dokumentai kitomis kalbomis

Prekės savybės Prekės savybės prancūzų 21-07-2017

Ieškokite perspėjimų, susijusių su šiuo produktu

Peržiūrėti dokumentų istoriją