MAR-QUETIAPINE TABLET (IMMEDIATE RELEASE)

Maa: Kanada

Kieli: englanti

Lähde: Health Canada

Osta se nyt

Valmisteyhteenveto Valmisteyhteenveto (SPC)
16-11-2022

Aktiivinen ainesosa:

QUETIAPINE (QUETIAPINE FUMARATE)

Saatavilla:

MARCAN PHARMACEUTICALS INC

ATC-koodi:

N05AH04

INN (Kansainvälinen yleisnimi):

QUETIAPINE

Annos:

100MG

Lääkemuoto:

TABLET (IMMEDIATE RELEASE)

Koostumus:

QUETIAPINE (QUETIAPINE FUMARATE) 100MG

Antoreitti:

ORAL

Kpl paketissa:

100/500

Prescription tyyppi:

Prescription

Terapeuttinen alue:

ATYPICAL ANTIPSYCHOTICS

Tuoteyhteenveto:

Active ingredient group (AIG) number: 0131858002; AHFS:

Valtuutuksen tilan:

APPROVED

Valtuutus päivämäärä:

2013-01-16

Valmisteyhteenveto

                                Page1 of58
PRODUCT MONOGRAPH
INCLUDING PATIENTMEDICATIONINFORMATION
Pr
MAR-QUETIAPINE
QuetiapineTablets
Immediate-ReleaseTablets,25, 100, 200 and300mg (asquetiapinefumarate),
OralUse
USP
AntipsychoticAgent
MarcanPharmaceuticals Inc.
2GurdwaraRoad,Suite#112
Ottawa,Ontario
K2E1A2 Canada
Date of InitialAuthorization:
JAN 16,2013
Date ofRevision:
NOV16,2022
SubmissionControl No.: 269102
Page2 of58
RECENT MAJORLABELCHANGES
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TABLE OF CONTENTS
Sectionsorsubsectionsthatare notapplicableat the time of authorization
are notlisted
1.
INDICATIONS
......................................................................................................................4
1.1
Pediatrics...............................................................................................................
4
1.2
Geriatrics
...............................................................................................................
4
2.
CONTRAINDICATIONS
.......................................................................................................4
3.
SERIOUS WARNINGS AND PRECAUTIONS BOX
......................................................... 5
4.
DOSAGE AND ADMINISTRATION
.....................................................................................5
4.1
Dosing
Considerations...................................................................................................
5
4.2
Recommended Dose and Dosage
Adjustment..........................................................5
4.4
Administration........................................................................................................
7
4.5
Missed
Dose...................................................................................................................
7
5.
OVERDOSAGE
........................................................................................................................
7
6.
DOSA
                                
                                Lue koko asiakirja
                                
                            

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Valmisteyhteenveto Valmisteyhteenveto ranska 16-11-2022

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