AMIODARONE TABLET

Krajina: Kanada

Jazyk: angličtina

Zdroj: Health Canada

Aktívna zložka:

AMIODARONE HYDROCHLORIDE

Dostupné z:

SIVEM PHARMACEUTICALS ULC

ATC kód:

C01BD01

INN (Medzinárodný Name):

AMIODARONE

Dávkovanie:

200MG

Forma lieku:

TABLET

Zloženie:

AMIODARONE HYDROCHLORIDE 200MG

Spôsob podávania:

ORAL

Počet v balení:

100

Typ predpisu:

Prescription

Terapeutické oblasti:

CLASS III ANTIARRYTHMICS

Prehľad produktov:

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

Stav Autorizácia:

APPROVED

Dátum Autorizácia:

2012-05-31

Súhrn charakteristických

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_Amiodarone _
_Page 1 of 65_
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PRODUCT MONOGRPAH
PR
AMIODARONE
Amiodarone Hydrochloride tablets, BP
200 mg
Antiarrhythmic Agent
SIVEM PHARMACEUTICALS ULC
Date of Revision:
4705 Dobrin Street
October 27, 2016
St. Laurent, Quebec
H4R 2P7
www.sivem.ca
Control number: 198891
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_Amiodarone _
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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........................................................................................................................................
23
DOSAGE
AND
ADMINISTRATION
....................................................................................................................
28
OVERDOSAGE
......................................................................................................................................................
30
ACTION
AND
CLINICAL
PHARMACOLOGY
...................................................................................................
31
STORAGE
AND
STABILITY
................................................................................................................................
34
SPECIAL
HANDLING
INSTRUCTIONS
....................................