IRBESARTAN TABLET

Pajjiż: Kanada

Lingwa: Ingliż

Sors: Health Canada

Ingredjent attiv:

IRBESARTAN

Disponibbli minn:

SIVEM PHARMACEUTICALS ULC

Kodiċi ATC:

C09CA04

INN (Isem Internazzjonali):

IRBESARTAN

Dożaġġ:

300MG

Għamla farmaċewtika:

TABLET

Kompożizzjoni:

IRBESARTAN 300MG

Rotta amministrattiva:

ORAL

Unitajiet fil-pakkett:

100/500

Tip ta 'preskrizzjoni:

Prescription

Żona terapewtika:

ANGIOTENSIN II RECEPTOR ANTAGONISTS

Sommarju tal-prodott:

Active ingredient group (AIG) number: 0131700003; AHFS:

L-istatus ta 'awtorizzazzjoni:

APPROVED

Data ta 'l-awtorizzazzjoni:

2012-05-25

Karatteristiċi tal-prodott

_IRBESARTAN _
_Page 1 of 37_
_ _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
IRBESARTAN
Irbesartan tablets
Tablets, 75 mg, 150 mg and 300 mg, Oral
USP
Angiotensin II AT
1
Receptor Blocker
Sivem Pharmaceuticals ULC
4705 Dobrin Street
Saint-Laurent, Quebec, Canada
H4R 2P7
www.sivem.ca
Date of Initial Authorization
MAY 25, 2012
Date of revision
JAN 02, 2024
Submission Control No.: 281898
_IRBESARTAN _
_Page 2 of 37_
_ _
RECENT MAJOR LABEL CHANGES
7. WARNINGS AND PRECAUTIONS
01/2024
TABLE OF CONTENTS
RECENT MAJOR LABEL
CHANGES………………………………………………………………………….…...............2
TABLES 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
......................................................... 5
4.4
Administration
..........................................................................................................
6
4.5
Missed Dose
...............................................