SANDOMIGRAN DS TABLET

Quốc gia: Canada

Ngôn ngữ: Tiếng Anh

Nguồn: Health Canada

Thành phần hoạt chất:

PIZOTIFEN (PIZOTIFEN MALATE)

Sẵn có từ:

PALADIN LABS INC.

Mã ATC:

N02CX01

INN (Tên quốc tế):

PIZOTIFEN

Liều dùng:

1MG

Dạng dược phẩm:

TABLET

Thành phần:

PIZOTIFEN (PIZOTIFEN MALATE) 1MG

Tuyến hành chính:

ORAL

Các đơn vị trong gói:

100

Loại thuốc theo toa:

Prescription

Khu trị liệu:

ANTIMIGRAINE AGENTS, MISCELLANEOUS

Tóm tắt sản phẩm:

Active ingredient group (AIG) number: 0110877001; AHFS:

Tình trạng ủy quyền:

APPROVED

Ngày ủy quyền:

2009-06-02

Đặc tính sản phẩm

_Product Monograph _
_ _
SANDOMIGRAN DS (_pizotifen tablets)_
_ _
_ Page 1 of 21_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
SANDOMIGRAN DS
Pizotifen tablets
Tablets, 1 mg pizotifen (as pizotifen malate), oral
Serotonin and Tryptamine Antagonist
Migraine Prophylaxis
ATC code: N02CX
Paladin Labs Inc.
100 Alexis Nihon Blvd., Suite 600
Saint-Laurent, Quebec, Canada
H4M 2P2
Date of Initial Authorization:
December 31, 1980
Date of Revision:
August 23, 2023
Version 5.0
Submission Control Number: 272965
_Product Monograph _
_ _
SANDOMIGRAN DS (_pizotifen tablets)_
_ _
_ Page 2 of 21_
RECENT MAJOR LABEL CHANGES
2 CONTRAINDICATIONS
08/2023
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
.................................................................................
5
4.1
Dosing Considerations
..............................................................................................
5
4.2
Recommended Dose and Dosage Adjustment
......................................................... 5
4.5
Missed Dose
..............................................