TEVA-DAPAGLIFLOZIN TABLET

Land: Canada

Taal: Engels

Bron: Health Canada

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Download Productkenmerken (SPC)
21-12-2021

Werkstoffen:

DAPAGLIFLOZIN

Beschikbaar vanaf:

TEVA CANADA LIMITED

ATC-code:

A10BK01

INN (Algemene Internationale Benaming):

DAPAGLIFLOZIN

Dosering:

10MG

farmaceutische vorm:

TABLET

Samenstelling:

DAPAGLIFLOZIN 10MG

Toedieningsweg:

ORAL

Eenheden in pakket:

100

Prescription-type:

Prescription

Product samenvatting:

Active ingredient group (AIG) number: 0156370002; AHFS:

Autorisatie-status:

APPROVED

Autorisatie datum:

2023-05-15

Productkenmerken

                                _Teva-Dapagliflozin Page 1 of 72_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
TEVA-DAPAGLIFLOZIN
dapagliflozin tablets
Tablets, 5 mg and 10 mg, Oral
ATC Code: A10BK01
Sodium-glucose co-transporter 2 (SGLT2) inhibitors
Teva Canada Limited
30 Novopharm Court
Toronto, Ontario M1B 2K9
Canada
Date of Initial Authorization:
DEC 21, 2021
Submission Control No: 246884
_Teva-Dapagliflozin Page 2 of 72_
RECENT MAJOR LABEL CHANGES
NOT APPLICABLE.
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
...........................................................................................................
5
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
4.5
Missed Dose
..................................
                                
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