XEOMIN POWDER FOR SOLUTION

국가: 캐나다

언어: 영어

출처: Health Canada

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Download 제품 특성 요약 (SPC)
03-10-2023

유효 성분:

INCOBOTULINUMTOXINA

제공처:

MERZ PHARMACEUTICALS GMBH

ATC 코드:

M03AX01

INN (국제 이름):

BOTULINUM TOXIN

복용량:

50UNIT

약제 형태:

POWDER FOR SOLUTION

구성:

INCOBOTULINUMTOXINA 50UNIT

관리 경로:

INTRAGLANDULAR

패키지 단위:

15G/50G

처방전 유형:

Prescription

치료 영역:

OTHER MISCELLANEOUS THERAPEUTIC AGENTS

제품 요약:

Active ingredient group (AIG) number: 0153613002; AHFS:

승인 상태:

APPROVED

승인 날짜:

2011-08-02

제품 특성 요약

                                _Xeomin_
_®_
_ (incobotulinumtoxinA) - Product Monograph _
_Page 1 of 58_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
XEOMIN
®
incobotulinumtoxinA for injection
Clostridium Botulinum Neurotoxin Type A (150 kD), free from complexing
proteins
50 and 100 units per vial
Intramuscular or intraglandular injection
Pharmaceutical Standard: House
Muscle relaxant, peripherally acting agent
Manufactured by:
Merz Pharmaceuticals GmbH
Eckenheimer Landstraße 100
60318 Frankfurt/Main
Germany
http://www.merz.com/company/merz_pharmaceuticals/
Imported and distributed by:
Merz Pharma Canada Ltd.
5515 North Service Road, Ste 202
Burlington, ON L7L 6G4
Date of Initial Authorization:
March 13, 2009
Date of Revision: October 3, 2023
Submission Control Number: 274814
_Xeomin_
_®_
_ (incobotulinumtoxinA) - Product Monograph _
_Page 2 of 58_
RECENT MAJOR LABEL CHANGES
1 INDICATIONS, Chronic Sialorrhea in Pediatric Patients
09/2022
1 INDICATIONS, Spasticity of the Upper Limb
03/2022
1.1 PEDIATRICS, Chronic Sialorrhea in Pediatric Patients
09/2022
3 SERIOUS WARNINGS AND PRECAUTIONS BOX
12/2022
4 DOSAGE AND ADMINISTRATION, 4.2 Recommended Dose and Dosage
Adjustment,
Chronic Sialorrhea in Pediatric Patients
09/2022
4 DOSAGE AND ADMINISTRATION, 4.2 Recommended Dose and Dosage
Adjustment,
Spasticity of the Upper Limb
03/2022
4 DOSAGE AND ADMINISTRATION,4.4, Administration, Chronic Sialorrhea
(pediatrics)
09/2022
7 WARNINGS AND PRECAUTIONS, 7.1.3 Pediatric Sialorrhea
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
.....................................................................
5
1
INDICATIONS
.....................................................................
                                
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