RIVA RIVAROXABAN TABLET

Land: Canada

Språk: engelsk

Kilde: Health Canada

Aktiv ingrediens:

RIVAROXABAN

Tilgjengelig fra:

LABORATOIRE RIVA INC.

ATC-kode:

B01AF01

INN (International Name):

RIVAROXABAN

Dosering :

10MG

Legemiddelform:

TABLET

Sammensetning:

RIVAROXABAN 10MG

Administreringsrute:

ORAL

Enheter i pakken:

15G/50G

Resept typen:

Prescription

Produkt oppsummering:

Active ingredient group (AIG) number: 0152487001; AHFS:

Autorisasjon status:

APPROVED

Autorisasjon dato:

2023-11-01

Preparatomtale

_Page 1 of 111_
_RIVA RIVAROXABAN (rivaroxaban)_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
RIVA RIVAROXABAN
Rivaroxaban Tablets
Tablets, 2.5 mg, 10 mg, 15 mg and 20 mg, Oral
House standard
Anticoagulant
(ATC Classification: B01AF01)
LABORATOIRE RIVA INC.
660 Boul. Industriel
Blainville, Quebec
J7C 3V4
www.labriva.com
Submission Control Number: 276851
Date of Initial Authorization:
AUG
25, 2023
_RIVA RIVAROXABAN (rivaroxaban) _
_ _
_Page 2 of 111_
RECENT MAJOR LABEL CHANGES
N/A
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
...................................................................................................................
5
2
CONTRAINDICATIONS
.................................................................................................
5
4
DOSAGE AND ADMINISTRATION
.................................................................................
5
4.1
Dosing Considerations
..............................................................................................
5
4.2
Recommended Dose and Dosage Adjustment
......................................................... 7
4.4
Administration
........................................................................................................
11
4.5
Missed Dose
..............................................................................