DOM-VENLAFAXINE XR CAPSULE (EXTENDED RELEASE)

Страна: Канада

Език: английски

Източник: Health Canada

Купи го сега

Активна съставка:

VENLAFAXINE (VENLAFAXINE HYDROCHLORIDE)

Предлага се от:

DOMINION PHARMACAL

АТС код:

N06AX16

INN (Международно Name):

VENLAFAXINE

дозиране:

37.5MG

Лекарствена форма:

CAPSULE (EXTENDED RELEASE)

Композиция:

VENLAFAXINE (VENLAFAXINE HYDROCHLORIDE) 37.5MG

Начин на приложение:

ORAL

Броя в опаковка:

500

Вид предписание :

Prescription

Терапевтична област:

SELECTIVE SEROTONIN AND NOREPINEPHRINE-REUPTAKE INHIBITORS

Каталог на резюме:

Active ingredient group (AIG) number: 0131294002; AHFS:

Статус Оторизация:

APPROVED

Дата Оторизация:

2013-05-17

Данни за продукта

                                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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Данни за продукта Данни за продукта френски 28-02-2013

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