TEVA-ZOLMITRIPTAN TABLET

国家: 加拿大

语言: 英文

来源: Health Canada

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06-04-2020

有效成分:

ZOLMITRIPTAN

可用日期:

TEVA CANADA LIMITED

ATC代码:

N02CC03

INN(国际名称):

ZOLMITRIPTAN

剂量:

2.5MG

药物剂型:

TABLET

组成:

ZOLMITRIPTAN 2.5MG

给药途径:

ORAL

每包单位数:

3/6/50

处方类型:

Prescription

治疗领域:

SELECTIVE SEROTONIN AGONISTS

產品總結:

Active ingredient group (AIG) number: 0134381001; AHFS:

授权状态:

APPROVED

授权日期:

2011-06-07

产品特点

                                PRODUCT MONOGRAPH
PR
TEVA-ZOLMITRIPTAN
(zolmitriptan) tablets
2.5 mg
PR
TEVA-ZOLMITRIPTAN OD
(zolmitriptan) orally disintegrating tablets
2.5 mg
Teva Standard
Migraine Therapy
5-HT
1
Receptor Agonist
Teva Canada Limited
30 Novopharm Court
Toronto, Ontario
M1B 2K9
www.tevacanada.com
Submission Control No: 237687
Date of Revision:
April 6, 2020
2
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
.........................................................................................................
12
DRUG INTERACTIONS
.........................................................................................................
18
DOSAGE AND ADMINISTRATION
.....................................................................................
19
OVERDOSAGE
.......................................................................................................................
21
ACTION AND CLINICAL PHARMACOLOGY
................................................................... 21
STORAGE AND STABILITY
.................................................................................................
24
DOSAGE FORMS, COMPOSITION AND PACKAGING
.................................................... 24
PART II: SCIENTIFIC INFORMATION
...............................................................................
25
PHARMACEUTICAL INFORMATION
.................................................................................
25
CLINICAL TRIALS
...........................................
                                
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