XARELTO TABLET

País: Canadá

Idioma: inglés

Fuente: Health Canada

Ingredientes activos:

RIVAROXABAN

Disponible desde:

BAYER INC

Código ATC:

B01AF01

Designación común internacional (DCI):

RIVAROXABAN

Dosis:

15MG

formulario farmacéutico:

TABLET

Composición:

RIVAROXABAN 15MG

Vía de administración:

ORAL

Unidades en paquete:

28/42/90

tipo de receta:

Prescription

Área terapéutica:

Direct Factor Xa Inhibitors

Resumen del producto:

Active ingredient group (AIG) number: 0152487002; AHFS:

Estado de Autorización:

APPROVED

Fecha de autorización:

2012-01-16

Ficha técnica

_XARELTO (rivaroxaban tablets; rivaroxaban granules for oral
suspension) _
_Page 1 of 119_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
XARELTO®
Rivaroxaban tablets
Tablets 2.5 mg, 10 mg, 15 mg and 20 mg, Oral
Rivaroxaban granules for oral suspension
Granules for oral suspension, 1mg/mL when reconstituted, Oral
Anticoagulant
(ATC Classification: B01AF01)
Bayer Inc.
2920 Matheson Boulevard East
Mississauga, Ontario
L4W 5R6
http://www.bayer.ca
Date of Initial Authorization:
SEP 15, 2008
Date of Revision:
April 17, 2023
Submission Control Number: 268349
© 2023, Bayer Inc.
®
TM see www.bayer.ca/tm-mc
_XARELTO (rivaroxaban tablets; rivaroxaban granules for oral
suspension) _
_Page 2 of 119_
RECENT MAJOR LABEL CHANGES
4 DOSAGE AND ADMINISTRATION, 4.3 Reconstitution
04/2023
7 WARNINGS AND PRECAUTIONS, Bleeding
12/2021
TABLE OF CONTENTS
SECTIONS OR SUBSECTIONS THAT ARE NOT APPLICABLE AT THE TIME OF
AUTHORIZATION ARE NOT LISTED.
RECENT MAJOR LABEL CHANGES
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2
TABLE OF CONTENTS
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2
PART I: HEALTH PROFESSIONAL INFORMATION
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4
1 INDICATIONS
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4
1.1 Pediatrics
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4
1.2 Geriatrics
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5
2 CONTRAINDICATIONS
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5
4 DOSAGE AND ADMINISTRATION
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