VIOKACE TABLET

Држава: Канада

Језик: Енглески

Извор: Health Canada

Активни састојак:

LIPASE; PROTEASE; AMYLASE

Доступно од:

NESTLE ENTERPRISES S.A.

АТЦ код:

A09AA02

INN (Међународно име):

MULTIENZYMES (LIPASE, PROTEASE ETC)

Дозирање:

20880UNIT; 112500UNIT; 113400UNIT

Фармацеутски облик:

TABLET

Састав:

LIPASE 20880UNIT; PROTEASE 112500UNIT; AMYLASE 113400UNIT

Пут администрације:

ORAL

Јединице у пакету:

100

Тип рецептора:

Prescription

Терапеутска област:

DIGESTANTS

Резиме производа:

Active ingredient group (AIG) number: 0302964043; AHFS:

Статус ауторизације:

APPROVED

Датум одобрења:

2020-07-02

Карактеристике производа

IMPORTANT: PLEASE READ
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_VIOKACE_
_TM_
_ – Pancrelipase Tablets _
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_Page 1 of 17_
PRODUCT MONOGRAPH
PR
VIOKACE
TM
Pancrelipase tablets
10,440 USP and 20,880 USP units of lipase
USP
Pancreatic enzymes
A09AA02
Nestlé Enterprises S.A.
12, rue Entre-deux-Villes
1800 Vevey, Switzerland
Distributed by:
Accelera Pharma Canada Inc. Mississauga, ON, L5L 5Z9
Date of Initial Approval:
March 25, 2015
Date of Revision:
July 3, 2020
Submission Control No: 239610
IMPORTANT: PLEASE READ
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_VIOKACE_
_TM_
_ – Pancrelipase Tablets _
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_Page 2 of 17_
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
...................................................................................................
5
DRUG INTERACTIONS
...................................................................................................
6
DOSAGE AND ADMINISTRATION
...............................................................................
7
OVERDOSAGE
..................................................................................................................
8
ACTION AND CLINICAL PHARMACOLOGY
.............................................................. 8
STORAGE AND STABILITY
...........................................................................................
8
SPECIAL HANDLING INSTRUCTIONS
.........................................................................
9
DOSAGE FORMS, COMPOSITION AND PACKAGING
..............................................