ACH-TELMISARTAN TABLET

Krajina: Kanada

Jazyk: angličtina

Zdroj: Health Canada

Kúpte ho teraz

Aktívna zložka:

TELMISARTAN

Dostupné z:

ACCORD HEALTHCARE INC

ATC kód:

C09CA07

INN (Medzinárodný Name):

TELMISARTAN

Dávkovanie:

80MG

Forma lieku:

TABLET

Zloženie:

TELMISARTAN 80MG

Spôsob podávania:

ORAL

Počet v balení:

15G/50G

Typ predpisu:

Prescription

Terapeutické oblasti:

ANGIOTENSIN II RECEPTOR ANTAGONISTS

Prehľad produktov:

Active ingredient group (AIG) number: 0138223002; AHFS:

Stav Autorizácia:

APPROVED

Dátum Autorizácia:

2021-03-05

Súhrn charakteristických

                                ACH-Telmisartan - Product Monograph
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Page 1 of 35
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
ACH-TELMISARTAN
Telmisartan Tablets
Tablet, 40 mg and 80 mg, Oral
Manufacturer’s Standard
Angiotensin II AT
1
Receptor Blocker
Accord Healthcare Inc.
3535 boul. St. Charles, Suite 704
Kirkland, QC, H9H 5B9
Canada
Date of Initial Authorization:
June 7, 2013
Date of Revision:
June 26, 2023
SUBMISSION CONTROL NUMBER: 271374
ACH-Telmisartan - Product Monograph
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Page 2 of 35
RECENT MAJOR LABEL CHANGES
2 CONTRAINDICATIONS
06/2023
7 WARNINGS AND PRECAUTIONS
06/2023
TABLE OF CONTENTS
SECTIONS OR SUBSECTIONS THAT ARE NOT APPLICABLE AT THE TIME OF
AUTHORIZATION ARE NOT LISTED.
RECENT MAJOR LABEL CHANGES
.............................................................................................
2
TABLE OF CONTENTS
...............................................................................................................
2
PART I: HEALTH PROFESSIONAL
INFORMATION.......................................................................
4
1
INDICATIONS
..................................................................................................................
4
1.1
Pediatrics
...............................................................................................................
4
1.2
Geriatrics
...............................................................................................................
4
2
CONTRAINDICATIONS.....................................................................................................
4
3
SERIOUS WARNINGS AND PRECAUTIONS BOX
................................................................ 5
4
DOSAGE AND ADMINISTRATION
....................................................................................
5
4.1
Dosing Considerations
............................................................................................
5
4.2
Recommended Dose and Dosage Adjustment
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