NERISONE OINTMENT

Quốc gia: Canada

Ngôn ngữ: Tiếng Anh

Nguồn: Health Canada

Thành phần hoạt chất:

DIFLUCORTOLONE VALERATE

Sẵn có từ:

GLAXOSMITHKLINE INC

Mã ATC:

D07AC06

INN (Tên quốc tế):

DIFLUCORTOLONE

Liều dùng:

0.1%

Dạng dược phẩm:

OINTMENT

Thành phần:

DIFLUCORTOLONE VALERATE 0.1%

Tuyến hành chính:

TOPICAL

Các đơn vị trong gói:

30G

Loại thuốc theo toa:

Prescription

Khu trị liệu:

ANTI-INFLAMMATORY AGENTS

Tóm tắt sản phẩm:

Active ingredient group (AIG) number: 0115864001; AHFS:

Tình trạng ủy quyền:

CANCELLED POST MARKET

Ngày ủy quyền:

2015-11-03

Đặc tính sản phẩm

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_Page 1 of 20_
PRODUCT MONOGRAPH
PR
NERISONE
®
(DIFLUCORTOLONE VALERATE)
Cream 0.1% w/w
Oily Cream 0.1% w/w
Ointment 0.1% w/w
THERAPEUTIC CLASSIFICATION
TOPICAL CORTICOSTEROID
GlaxoSmithKline Inc.
7333 Mississauga Road
Mississauga, Ontario
L5N 6L4
www.stiefel.ca
Date of Revision:
October 29, 2014
Submission Control No: 175615
_©2014 GlaxoSmithKline Inc., All Rights Reserved _
_®NERISONE is a trade mark of Bayer Schering Pharma
Aktiengesellschaft. _
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_Page 2 of 20_
TABLE OF CONTENTS
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PAGE
PART I: HEALTH PROFESSIONAL
INFORMATION................................................... 3
SUMMARY PRODUCT INFORMATION
................................................................... 3
INDICATIONS AND CLINICAL USE
.........................................................................
3
CONTRAINDICATIONS
..............................................................................................
4
WARNINGS AND PRECAUTIONS
.............................................................................
4
ADVERSE REACTIONS
...............................................................................................
8
DRUG INTERACTIONS
...............................................................................................
8
DOSAGE AND ADMINISTRATION
...........................................................................
9
ACTION AND CLINICAL PHARMACOLOGY
....................................................... 11
STORAGE AND STABILITY
.....................................................................................
12
DOSAGE FORMS, COMPOSITION AND PACKAGING
........................................ 12
PART II: SCIENTIFIC INFORMATION
........................................................................
13
PHARMACEUTICAL INFORMATION
.....................................................................
13
REFERENCES
.............................................................................................................
16
PART III: CONSUMER INFORMATION
............