EYLEA SOLUTION

Land: Canada

Sprog: engelsk

Kilde: Health Canada

Køb det nu

Hent Produktets egenskaber (SPC)
29-06-2023

Aktiv bestanddel:

AFLIBERCEPT

Tilgængelig fra:

BAYER INC

ATC-kode:

S01LA05

INN (International Name):

AFLIBERCEPT

Dosering:

2MG

Lægemiddelform:

SOLUTION

Sammensætning:

AFLIBERCEPT 2MG

Indgivelsesvej:

INTRAVITREAL

Enheder i pakken:

278 MICROLITERS

Recept type:

Prescription

Terapeutisk område:

EENT DRUGS, MISCELLANEOUS

Produkt oversigt:

Active ingredient group (AIG) number: 0154950001; AHFS:

Autorisation status:

APPROVED

Autorisation dato:

2013-11-08

Produktets egenskaber

                                _EYLEA Aflibercept Injection _
_Page 1 of 70_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
EYLEA
®
Aflibercept injection
Single Use Pre-filled Syringes and Single Use Vials for the Treatment
of a Single Eye
2 mg / 0.05 mL Solution for Intravitreal Injection
Ophthalmological / Antineovascularization agent
ATC Code: S01LA05
Bayer Inc.
2920 Matheson Boulevard East
Mississauga, Ontario
L4W 5R6
http://www.bayer.ca
Date of Initial Authorization:
NOV 08, 2013
Date of Revision:
JUN 29, 2023
Submission Control Number: 266439
© 2023, Bayer Inc.
®
TM see www.bayer.ca/tm-mc
_EYLEA Aflibercept Injection _
_Page 2 of 70_
RECENT MAJOR LABEL CHANGES
4 DOSAGE AND ADMINISTRATION, 4.2 Recommended Dose and
Dosage Adjustment
06/2023
4 DOSAGE AND ADMINISTRATION, 4.4 Administration
11/2022
TABLE OF CONTENTS
SECTIONS OR SUBSECTIONS THAT ARE NOT APPLICABLE AT THE TIME OF
AUTHORIZATION ARE NOT LISTED
.
RECENT MAJOR LABEL CHANGES
.........................................................................................
2
TABLE OF CONTENTS ...........................................................................................................
2
PART I: HEALTH PROFESSIONAL INFORMATION .................................................................. 4
1 INDICATIONS
....................................................................................................................
4
1.1 Pediatrics
.......................................................................................................................
4
1.2 Geriatrics
.......................................................................................................................
4
2 CONTRAINDICATIONS ......................................................................................................
4
4 DOSAGE AND ADMINISTRATION ......................................................................................
4
4.1 Dosing Considerations
....................................................................................................
4
4.2 
                                
                                Læs hele dokumentet
                                
                            

Dokumenter på andre sprog

Produktets egenskaber Produktets egenskaber fransk 29-06-2023

Søg underretninger relateret til dette produkt