ENTERIC COATED DAILY LOW DOSE ASA 81 MG TABLET (DELAYED-RELEASE)

Valsts: Kanāda

Valoda: angļu

Klimata pārmaiņas: Health Canada

Nopērc to tagad

Lejuplādēt Produkta apraksts (SPC)
23-03-2022

Aktīvā sastāvdaļa:

ACETYLSALICYLIC ACID

Pieejams no:

VITA HEALTH PRODUCTS INC

ATĶ kods:

B01AC06

SNN (starptautisko nepatentēto nosaukumu):

ACETYLSALICYLIC ACID

Deva:

81MG

Zāļu forma:

TABLET (DELAYED-RELEASE)

Kompozīcija:

ACETYLSALICYLIC ACID 81MG

Ievadīšanas:

ORAL

Vienības iepakojumā:

30/120/180/300

Receptes veids:

OTC

Ārstniecības joma:

SALICYLATES

Produktu pārskats:

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

Autorizācija statuss:

APPROVED

Autorizācija datums:

2011-02-17

Produkta apraksts

                                ASA 81 mg Page 1 of 46
PRODUCT MONOGRAPH
ASA 81 MG
Acetylsalicylic Acid Delayed Release Tablets
81 mg
USP
Platelet aggregation inhibitor
Vita Health Products Inc.
150 Beghin Avenue
Winnipeg, MB
Canada R2J 3W2
Control Number: 261087
Date of Preparation:
February 3, 2011
Date of Revision :
March 23, 2022
ASA 81 mg Page 2 of 46
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
...............................................................................................................
7
DRUG INTERACTIONS
...............................................................................................................
7
DOSAGE AND ADMINISTRATION
...........................................................................................
9
OVERDOSAGE
...........................................................................................................................
10
ACTION AND CLINICAL PHARMACOLOGY
.......................................................................
11
STORAGE AND STABILITY
.....................................................................................................
13
DOSAGE FORMS, COMPOSITION AND PACKAGING
........................................................ 13
PART II: SCIENTIFIC INFORMATION
..............................................................................
14
PHARMACEUTICAL INFORMATION
.....................................................................................
14
CLINICAL TRIALS
..............
                                
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