AMIODARONE OMEGA SOLUTION

Maa: Kanada

Kieli: englanti

Lähde: Health Canada

Osta se nyt

Valmisteyhteenveto Valmisteyhteenveto (SPC)
04-06-2018

Aktiivinen ainesosa:

AMIODARONE HYDROCHLORIDE

Saatavilla:

OMEGA LABORATORIES LIMITED

ATC-koodi:

C01BD01

INN (Kansainvälinen yleisnimi):

AMIODARONE

Annos:

50MG

Lääkemuoto:

SOLUTION

Koostumus:

AMIODARONE HYDROCHLORIDE 50MG

Antoreitti:

INTRAVENOUS

Kpl paketissa:

100

Prescription tyyppi:

Prescription

Terapeuttinen alue:

CLASS III ANTIARRYTHMICS

Tuoteyhteenveto:

Active ingredient group (AIG) number: 0118593002; AHFS:

Valtuutuksen tilan:

APPROVED

Valtuutus päivämäärä:

2004-04-05

Valmisteyhteenveto

                                _Amiodarone Omega _
_Page 1 of 59 _
PRODUCT MONOGRAPH PR
AMIODARONE OMEGA
Amiodarone hydrochloride for injection
House Standard
Vials: 50 mg/mL
Antiarrhythmic Agent
Omega Laboratories Limited.
Date of Revision: June 4, 2018
11 177 Hamon
Montreal, Quebec
H3M 3E4
Control Number: 213232
_Amiodarone Omega _
_Page 2 of 59 _
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
.......................................................................................................................
15
DRUG INTERACTIONS
.......................................................................................................................
18
DOSAGE AND ADMINISTRATION
...................................................................................................
22
OVERDOSAGE
.....................................................................................................................................
26
ACTION AND CLINICAL PHARMACOLOGY
..................................................................................
27
STORAGE AND STABILITY
...............................................................................................................
30
SPECIAL HANDLING INSTRUCTIONS
.............................................................................................
30
DOSAGE FORMS, COMPOSITION AND PACKAGING
................................................................... 30
PART II: SCIENT
                                
                                Lue koko asiakirja
                                
                            

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