MYLAN-VENLAFAXINE XR CAPSULE (EXTENDED RELEASE)

国家: 加拿大

语言: 英文

来源: Health Canada

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17-05-2018

有效成分:

VENLAFAXINE (VENLAFAXINE HYDROCHLORIDE)

可用日期:

MYLAN PHARMACEUTICALS ULC

ATC代码:

N06AX16

INN(国际名称):

VENLAFAXINE

剂量:

37.5MG

药物剂型:

CAPSULE (EXTENDED RELEASE)

组成:

VENLAFAXINE (VENLAFAXINE HYDROCHLORIDE) 37.5MG

给药途径:

ORAL

每包单位数:

100/500

处方类型:

Prescription

治疗领域:

SELECTIVE SEROTONIN AND NOREPINEPHRINE-REUPTAKE INHIBITORS

產品總結:

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

授权状态:

CANCELLED POST MARKET

授权日期:

2018-02-07

产品特点

                                PAGE 1 OF 62
PRODUCT MONOGRAPH
PR
MYLAN-VENLAFAXINE XR CAPSULES
(VENLAFAXINE HYDROCHLORIDE)
EXTENDED RELEASE CAPSULES
(37.5 MG, 75 MG, AND 150 MG VENLAFAXINE AS VENLAFAXINE HYDROCHLORIDE)
ANTIDEPRESSANT
Mylan Pharmaceuticals ULC
Date of Revision:
85 Advance Rd.
May 17, 2018
Etobicoke, Ontario
M8Z 2S6
Submission Control No.: 215657
PAGE 2 OF 62
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
.........................................................................................................
16
DRUG INTERACTIONS
.........................................................................................................
29
DOSAGE AND ADMINISTRATION
.....................................................................................
36
OVERDOSAGE
.......................................................................................................................
39
ACTION AND CLINICAL PHARMACOLOGY
................................................................... 41
STORAGE AND STABILITY
.................................................................................................
45
SPECIAL HANDLING INSTRUCTIONS
..............................................................................
45
DOSAGE FORMS, COMPOSITION AND PACKAGING
.................................................... 45
PART II: SCIENTIFIC INFORMATION
....................................................................................
47
PHARMACEUTICAL INFORMATION
.......................
                                
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