PRO-AMIODARONE - 200 TABLET

Quốc gia: Canada

Ngôn ngữ: Tiếng Anh

Nguồn: Health Canada

Thành phần hoạt chất:

AMIODARONE HYDROCHLORIDE

Sẵn có từ:

PRO DOC LIMITEE

Mã ATC:

C01BD01

INN (Tên quốc tế):

AMIODARONE

Liều dùng:

200MG

Dạng dược phẩm:

TABLET

Thành phần:

AMIODARONE HYDROCHLORIDE 200MG

Tuyến hành chính:

ORAL

Các đơn vị trong gói:

100

Loại thuốc theo toa:

Prescription

Khu trị liệu:

CLASS III ANTIARRYTHMICS

Tóm tắt sản phẩm:

Active ingredient group (AIG) number: 0118593001; AHFS:

Tình trạng ủy quyền:

APPROVED

Ngày ủy quyền:

2008-05-21

Đặc tính sản phẩm

Page 1 of 65
PRODUCT MONOGRAPH
PRO-AMIODARONE - 200
AMIODARONE TABLETS BP
200 MG AMIODARONE HYDROCHLORIDE
ANTIARRHYTHMIC AGENT
PRO DOC LTÉE
DATE OF REVISION:
2925, boul. Industriel
September 15, 2017
Laval, Quebec
H7L 3W9
SUBMISSION CONTROL NO: 209239
Page 2 of 65
TABLE OF CONTENTS
PART I:HEALTH PROFESSIONAL INFORMATION
......................................................... 3
SUMMARY PRODUCT INFORMATION
............................................................................
3
INDICATIONS AND CLINICAL USE
..................................................................................
3
CONTRAINDICATIONS
.......................................................................................................
4
WARNINGS AND PRECAUTIONS
......................................................................................
4
ADVERSE REACTIONS
......................................................................................................
19
DRUG INTERACTIONS
......................................................................................................
25
DOSAGE AND ADMINISTRATION
..................................................................................
30
OVERDOSAGE
....................................................................................................................
32
ACTION AND CLINICAL PHARMACOLOGY
................................................................ 33
STORAGE AND STABILITY
..............................................................................................
37
DOSAGE FORMS, COMPOSITION AND PACKAGING
................................................. 37
PART II: SCIENTIFIC INFORMATION
..............................................................................
38
PHARMACEUTICAL INFORMATION
..............................................................................
38
CLINICAL TRIALS
..............................................................................................................
38
DETAILED PHARMACOLOGY
..........................