TEVA-TELMISARTAN HCTZ TABLET

Krajina: Kanada

Jazyk: angličtina

Zdroj: Health Canada

Kúpte ho teraz

Aktívna zložka:

TELMISARTAN (TELMISARTAN SODIUM); HYDROCHLOROTHIAZIDE

Dostupné z:

TEVA CANADA LIMITED

ATC kód:

C09DA07

INN (Medzinárodný Name):

TELMISARTAN AND DIURETICS

Dávkovanie:

80MG; 12.5MG

Forma lieku:

TABLET

Zloženie:

TELMISARTAN (TELMISARTAN SODIUM) 80MG; HYDROCHLOROTHIAZIDE 12.5MG

Spôsob podávania:

ORAL

Počet v balení:

30/100/500

Typ predpisu:

Prescription

Terapeutické oblasti:

ANGIOTENSIN II RECEPTOR ANTAGONISTS

Prehľad produktov:

Active ingredient group (AIG) number: 0244783001; AHFS:

Stav Autorizácia:

APPROVED

Dátum Autorizácia:

2012-02-06

Súhrn charakteristických

                                _ _
TEVA-TELMISARTAN HCTZ
_ _
Page 1 of 72
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
TEVA-TELMISARTAN HCTZ
Telmisartan and Hydrochlorothiazide Tablets
Tablet, 80 mg Telmisartan (as Telmisartan Sodium) / 12.5 mg
Hydrochlorothiazide, Oral
Tablet, 80 mg Telmisartan (as Telmisartan Sodium) / 25 mg
Hydrochlorothiazide, Oral
Teva standard
Angiotensin II AT
1
Receptor Blocker / Diuretic
Teva Canada Limited
30 Novopharm Court
Toronto, ON
M1B 2K9
Canada
www.tevacanada.com
Date of Initial Authorization:
February 6, 2012
Date of Revision:
February 24, 2023
Submission Control Number: 267285
_ _
TEVA-TELMISARTAN HCTZ
_ _
Page 2 of 72
RECENT MAJOR LABEL CHANGES
2 CONTRAINDICATIONS
10/2021
7 WARNINGS AND PRECAUTIONS
02/2023
4 DOSAGE AND ADMINISTRATION
02/2023
7 WARNINGS AND PRECAUTIONS
02/2023
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
Dos
                                
                                Prečítajte si celý dokument
                                
                            

Dokumenty v iných jazykoch

Súhrn charakteristických Súhrn charakteristických francúzština 24-02-2023