MYLAN-AMIODARONE TABLET

国家: 加拿大

语言: 英文

来源: Health Canada

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下载 产品特点 (SPC)
22-04-2016

有效成分:

AMIODARONE HYDROCHLORIDE

可用日期:

MYLAN PHARMACEUTICALS ULC

ATC代码:

C01BD01

INN(国际名称):

AMIODARONE

剂量:

200MG

药物剂型:

TABLET

组成:

AMIODARONE HYDROCHLORIDE 200MG

给药途径:

ORAL

每包单位数:

100

处方类型:

Prescription

治疗领域:

CLASS III ANTIARRYTHMICS

產品總結:

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

授权状态:

CANCELLED POST MARKET

授权日期:

2018-07-12

产品特点

                                PAGE 1 OF 64
PRODUCT MONOGRAPH
PR
MYLAN-AMIODARONE
(Amiodarone Hydrochloride Tablets, BP)
200 MG
Antiarrhythmic Agent
Mylan Pharmaceuticals ULC
Date of revision:
85 Advance Road
April 14, 2016
Etobicoke, Ontario
M8Z 2S6
Control number: 193651
PAGE 2 OF 64
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
........................................................ 3
SUMMARY
PRODUCT
INFORMATION
................................................................................
3
INDICATIONS
AND
CLINICAL
USE
.....................................................................................
3
CONTRAINDICATIONS
..........................................................................................................
4
WARNINGS
AND
PRECAUTIONS
.........................................................................................
5
ADVERSE
REACTIONS
.........................................................................................................
20
DRUG
INTERACTIONS
.........................................................................................................
23
DOSAGE
AND
ADMINISTRATION
.....................................................................................
29
OVERDOSAGE
.......................................................................................................................
31
ACTION
AND
CLINICAL
PHARMACOLOGY
....................................................................
32
STORAGE
AND
STABILITY
...............................................................................................
36
SPECIAL
HANDLING
INSTRUCTIONS
...........................................................................
36
DOSAGE
FORMS,
COMPOSITION
AND
PACKAGING
................................................ 36
PART II: SCIENTIFIC INFORMATION
..............................................................................
37
PHARMACEUTICAL
INFORMATION
.................................................................................
37
CLINICAL
TRIALS
...............................
                                
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