APO-TELMISARTAN-AMLODIPINE TABLET

Pays: Canada

Langue: anglais

Source: Health Canada

Achète-le

Ingrédients actifs:

TELMISARTAN; AMLODIPINE (AMLODIPINE BESYLATE)

Disponible depuis:

APOTEX INC

Code ATC:

C09DB04

DCI (Dénomination commune internationale):

TELMISARTAN AND AMLODIPINE

Dosage:

40MG; 10MG

forme pharmaceutique:

TABLET

Composition:

TELMISARTAN 40MG; AMLODIPINE (AMLODIPINE BESYLATE) 10MG

Mode d'administration:

ORAL

Unités en paquet:

30/100/500

Type d'ordonnance:

Prescription

Domaine thérapeutique:

ANGIOTENSIN II RECEPTOR ANTAGONISTS

Descriptif du produit:

Active ingredient group (AIG) number: 0252947002; AHFS:

Statut de autorisation:

APPROVED

Date de l'autorisation:

2020-09-04

Résumé des caractéristiques du produit

                                _Product Monograph _
_APO-TELMISARTAN-AMLODIPINE (telmisartan/amlodipine) _
_Page 1 of 59 _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
APO-TELMISARTAN-AMLODIPINE
Telmisartan / Amlodipine Tablets
Tablets, 40/5 mg, 40/10 mg, 80/5 mg and 80/10 mg telmisartan /
amlodipine (as amlodipine
besylate), Oral
House Standard
Angiotensin II AT1 Receptor Blocker / Calcium Channel Blocker
APOTEX INC.
150 Signet Drive
Toronto, Ontario
M9L 1T9
Date of Initial Authorization
FEB 27, 2018
Date of Revision:
OCT 16, 2023
Submission Control Number: 274810
_Product Monograph _
_APO-TELMISARTAN-AMLODIPINE (telmisartan/amlodipine) _
_Page 2 of 59 _
RECENT MAJOR LABEL CHANGES
4 DOSAGE AND ADMINISTRATION
10/2023
7 WARNINGS AND PRECAUTIONS
10/2023
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
......................
                                
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