POTELIGEO SOLUTION

Pajjiż: Kanada

Lingwa: Ingliż

Sors: Health Canada

Ixtrih issa

Ingredjent attiv:

MOGAMULIZUMAB

Disponibbli minn:

KYOWA KIRIN, INC.

Kodiċi ATC:

L01FX09

INN (Isem Internazzjonali):

MOGAMULIZUMAB

Dożaġġ:

4MG

Għamla farmaċewtika:

SOLUTION

Kompożizzjoni:

MOGAMULIZUMAB 4MG

Rotta amministrattiva:

INTRAVENOUS

Unitajiet fil-pakkett:

100

Tip ta 'preskrizzjoni:

Schedule D

Sommarju tal-prodott:

Active ingredient group (AIG) number: 0163781001; AHFS:

L-istatus ta 'awtorizzazzjoni:

APPROVED

Data ta 'l-awtorizzazzjoni:

2022-06-02

Karatteristiċi tal-prodott

                                _POTELIGEO (mogamulizumab for injection) _
_Page 1 of 25_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
Pr
POTELIGEO
®
Mogamulizumab for injection
20 mg/5 mL single-use vial
Intravenous Infusion, 4 mg/mL
Antineoplastic
ATC Code: L01FX09
Kyowa Kirin, Inc.
135 Route 202/206, Suite 6
Bedminster, NJ 07921 USA
www.kyowakirin.ca
DISTRIBUTOR:
Innomar Strategies
3470 Superior Court
Oakville, ON
L6L 0C4
http://www.innomar-strategies.com
Date of Initial Authorization:
June 2, 2022
Date of Revision:
June 20, 2022
Submission Control Number: 251277
_ _
_POTELIGEO (mogamulizumab for injection) _
_Page 2 of 25_
RECENT MAJOR LABEL CHANGES
N/A
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.......................................................4
4.3
Reconstitution
...........................................................................
                                
                                Aqra d-dokument sħiħ
                                
                            

Dokumenti f'lingwi oħra

Karatteristiċi tal-prodott Karatteristiċi tal-prodott Franċiż 20-06-2022

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