DOM-VENLAFAXINE XR CAPSULE (EXTENDED RELEASE)

Maa: Kanada

Kieli: englanti

Lähde: Health Canada

Osta se nyt

Lataa Valmisteyhteenveto (SPC)
28-02-2013

Aktiivinen ainesosa:

VENLAFAXINE (VENLAFAXINE HYDROCHLORIDE)

Saatavilla:

DOMINION PHARMACAL

ATC-koodi:

N06AX16

INN (Kansainvälinen yleisnimi):

VENLAFAXINE

Annos:

150MG

Lääkemuoto:

CAPSULE (EXTENDED RELEASE)

Koostumus:

VENLAFAXINE (VENLAFAXINE HYDROCHLORIDE) 150MG

Antoreitti:

ORAL

Kpl paketissa:

500

Prescription tyyppi:

Prescription

Terapeuttinen alue:

SELECTIVE SEROTONIN AND NOREPINEPHRINE-REUPTAKE INHIBITORS

Tuoteyhteenveto:

Active ingredient group (AIG) number: 0131294005; AHFS:

Valtuutuksen tilan:

APPROVED

Valtuutus päivämäärä:

2013-05-17

Valmisteyhteenveto

                                PRODUCT MONOGRAPH
PR
DOM-VENLAFAXINE XR
VENLAFAXINE HYDROCHLORIDE EXTENDED-RELEASE CAPSULES
37.5 MG, 75 MG AND 150 MG VENLAFAXINE, AS VENLAFAXINE HYDROCHLORIDE
Antidepressant
DOMINION PHARMACAL
6111 Royalmount Ave, Suite 100
Montréal, Québec
H4P 2T4
DATE OF REVISION:
February 28, 2013
Submission Control No: 116569, 151422, 162398
_ _
_Dom-VENLAFAXINE XR Product Monograph _
_Page 2 of 54 _
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
..................................................................................................23
DOSAGE AND ADMINISTRATION
..............................................................................30
OVERDOSAGE
................................................................................................................33
ACTION AND CLINICAL PHARMACOLOGY
............................................................34
STORAGE AND STABILITY
..........................................................................................37
SPECIAL HANDLING INSTRUCTIONS
.......................................................................37
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................38
PART II: SCIENTIFIC INFORMATION
...............................................................................39
PHARMACEUTICAL INFORMATION
..........................................................................39
CLINI
                                
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Valmisteyhteenveto Valmisteyhteenveto ranska 28-02-2013

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