AIMOVIG SOLUTION

Šalis: Kanada

kalba: anglų

Šaltinis: Health Canada

Nusipirk tai dabar

Prekės savybės Prekės savybės (SPC)
27-10-2022

Veiklioji medžiaga:

ERENUMAB

Prieinama:

NOVARTIS PHARMACEUTICALS CANADA INC

ATC kodas:

N02CD01

INN (Tarptautinis Pavadinimas):

ERENUMAB

Dozė:

70MG

Vaisto forma:

SOLUTION

Sudėtis:

ERENUMAB 70MG

Vartojimo būdas:

SUBCUTANEOUS

Vienetai pakuotėje:

(1X1 ML) AND (2X1ML)

Recepto tipas:

Prescription

Gydymo sritis:

CALCITONIN-GENE-RELATED PEPTIDE (CGRP) ANTAGONISTS

Produkto santrauka:

Active ingredient group (AIG) number: 0160530001; AHFS:

Autorizacija statusas:

APPROVED

Leidimo data:

2018-08-01

Prekės savybės

                                _AIMOVIG® (erenumab) _
_Page 1 of 63 _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
AIMOVIG®
(erenumab injection)
Solution for Injection, 70 mg/mL, for subcutaneous use
Solution for Injection, 140 mg/mL, for subcutaneous use
Professed Standard
Anti-Calcitonin gene-related peptide receptor (anti-CGRPR)
Novartis Pharmaceuticals Canada Inc.
385 Bouchard Blvd.
Dorval, Quebec
H9S 1A9
Date of Initial Authorization:
August 01, 2018
Date of Revision:
October 27, 2022
Submission Control Number: 264464
® AIMOVIG & SureClick are registered trademarks of Amgen Inc. used
under license by
Novartis Pharmaceuticals Canada Inc.
_ _
_AIMOVIG® (erenumab) _
_Page 2 of 63_
RECENT MAJOR LABEL CHANGES
7.0 WARNINGS AND PRECAUTIONS, Constipation with Serious
Complications
09/2022
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
Recommended Dose and Dosage
Adjustment.............
                                
                                Perskaitykite visą dokumentą
                                
                            

Dokumentai kitomis kalbomis

Prekės savybės Prekės savybės prancūzų 27-10-2022

Ieškokite perspėjimų, susijusių su šiuo produktu

Peržiūrėti dokumentų istoriją