ASA 81 MG TABLET (DELAYED-RELEASE)

Země: Kanada

Jazyk: angličtina

Zdroj: Health Canada

Aktivní složka:

ACETYLSALICYLIC ACID

Dostupné s:

LABORATOIRES TRIANON INC.

ATC kód:

B01AC06

INN (Mezinárodní Name):

ACETYLSALICYLIC ACID

Dávkování:

81MG

Léková forma:

TABLET (DELAYED-RELEASE)

Složení:

ACETYLSALICYLIC ACID 81MG

Podání:

ORAL

Jednotky v balení:

120/150/300

Druh předpisu:

OTC

Terapeutické oblasti:

SALICYLATES

Přehled produktů:

Active ingredient group (AIG) number: 0101169013; AHFS:

Stav Autorizace:

APPROVED

Datum autorizace:

2015-12-11

Charakteristika produktu

_ASA 81 MG - Product Monograph _
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_Page 1 of 44 _
PRODUCT MONOGRAPH
ASA 81 MG
Acetylsalicylic
Acid Delayed Release Tablets
81 mg
USP
Platelet aggregation inhibitor
LABORATOIRES TRIANON INC.
660 Boul. Industriel
Blainville,
Quebec
J7C 3V4
www.labriva.com
Date of Preparation:
December 11, 2015
Date of Revision:
September 28, 2022
Control Number: 267165
_ASA 81 MG - Product Monograph _
_ _
_Page 2 of 44 _
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.............................................................................................
6
DRUG INTERACTIONS
.............................................................................................
7
DOSAGE AND ADMINISTRATION
..........................................................................
9
OVERDOSAGE
.........................................................................................................10
ACTION AND CLINICAL
PHARMACOLOGY.........................................................11
STORAGE AND STABILITY
....................................................................................12
DOSAGE FORMS, COMPOSITION AND PACKAGING
..........................................12
PART II: SCIENTIFIC INFORMATION
..........................................................................
13
PHARMACEUTICAL INFORMATION
.....................................................................13
CLINICAL TRIALS
...................................................................................................14
DETAILED
PHARMACOLOGY.......................