RIVA-ZOLMITRIPTAN TABLET

Држава: Канада

Језик: Енглески

Извор: Health Canada

Активни састојак:

ZOLMITRIPTAN

Доступно од:

LABORATOIRE RIVA INC.

АТЦ код:

N02CC03

INN (Међународно име):

ZOLMITRIPTAN

Дозирање:

2.5MG

Фармацеутски облик:

TABLET

Састав:

ZOLMITRIPTAN 2.5MG

Пут администрације:

ORAL

Јединице у пакету:

6/30

Тип рецептора:

Prescription

Терапеутска област:

SELECTIVE SEROTONIN AGONISTS

Резиме производа:

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

Статус ауторизације:

CANCELLED POST MARKET

Датум одобрења:

2019-03-05

Карактеристике производа

PRODUCT MONOGRAPH
PR
(ZOLMITRIPTAN FILM-COATED TABLETS)
RIVA-ZOLMITRIPTAN
2.5 MG
5-HT1 RECEPTOR AGONIST
MIGRAINE THERAPY
LABORATOIRE RIVA INC.
660 Boul. Industriel
Blainville, Québec, Canada.
J7C 3V4
www.labriva.com
Date of Revision:
August 25, 2015
Submission Control #: 186807
_RIVA-ZOLMITRIPTAN Product Monograph _
_Page 2 of 36 _
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION .........................................................3
SUMMARY PRODUCT INFORMATION
........................................................................3
INDICATIONS AND CLINICAL USE
..............................................................................3
CONTRAINDICATIONS
...................................................................................................4
WARNINGS AND PRECAUTIONS
..................................................................................5
ADVERSE REACTIONS
..................................................................................................11
DRUG INTERACTIONS
..................................................................................................17
DOSAGE AND ADMINISTRATION
..............................................................................19
OVERDOSAGE
................................................................................................................20
ACTION AND CLINICAL PHARMACOLOGY
............................................................20
STORAGE AND STABILITY
..........................................................................................23
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................23
PART II: SCIENTIFIC INFORMATION ...............................................................................24
PHARMACEUTICAL INFORMATION
..........................................................................24
CLINICAL TRIALS
..........................................................................................................25
DETAILED PHARMACOLOGY
......................