AURO-TELMISARTAN HCTZ TABLET

Valsts: Kanāda

Valoda: angļu

Klimata pārmaiņas: Health Canada

Nopērc to tagad

Lejuplādēt Produkta apraksts (SPC)
26-01-2023

Aktīvā sastāvdaļa:

TELMISARTAN; HYDROCHLOROTHIAZIDE

Pieejams no:

AURO PHARMA INC

ATĶ kods:

C09DA07

SNN (starptautisko nepatentēto nosaukumu):

TELMISARTAN AND DIURETICS

Deva:

80MG; 12.5MG

Zāļu forma:

TABLET

Kompozīcija:

TELMISARTAN 80MG; HYDROCHLOROTHIAZIDE 12.5MG

Ievadīšanas:

ORAL

Vienības iepakojumā:

30/100/500/1000

Receptes veids:

Prescription

Ārstniecības joma:

ANGIOTENSIN II RECEPTOR ANTAGONISTS

Produktu pārskats:

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

Autorizācija statuss:

APPROVED

Autorizācija datums:

2016-07-18

Produkta apraksts

                                _Auro-Telmisartan HCTZ Product Monograph _Page 1 of 64
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
AURO-TELMISARTAN HCTZ
Telmisartan and Hydrochlorothiazide Tablets, USP
Tablet, 80 mg/12.5 mg and 80 mg/25 mg, Oral
Angiotensin II AT
1
Receptor Blocker/ Diuretic
Auro Pharma Inc.
3700 Steeles Avenue West, Suite # 402
Woodbridge, Ontario, L4L 8K8,
Canada
Date of initial Authorization:
July 18, 2016
Date of Revision:
January 26, 2023
Submission Control No: 267665
_Auro-Telmisartan HCTZ Product Monograph _Page 2 of 64
RECENT MAJOR LABEL CHANGES
2 CONTRAINDICATIONS
01 / 2023
7 WARNINGS AND PRECAUTIONS
01 / 2023
4 DOSAGE AND ADMINISTRATION
01 / 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
...................................................
                                
                                Izlasiet visu dokumentu
                                
                            

Dokumenti citās valodās

Produkta apraksts Produkta apraksts franču 26-01-2023