UPTRAVI TABLET

Země: Kanada

Jazyk: angličtina

Zdroj: Health Canada

Aktivní složka:

SELEXIPAG

Dostupné s:

JANSSEN INC

ATC kód:

B01AC27

INN (Mezinárodní Name):

SELEXIPAG

Dávkování:

600MCG

Léková forma:

TABLET

Složení:

SELEXIPAG 600MCG

Podání:

ORAL

Jednotky v balení:

60

Druh předpisu:

Prescription

Terapeutické oblasti:

VASODILATING AGENTS

Přehled produktů:

Active ingredient group (AIG) number: 0157750003; AHFS:

Stav Autorizace:

APPROVED

Datum autorizace:

2016-01-20

Charakteristika produktu

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PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
UPTRAVI
®
Selexipag Film-coated tablets
200 mcg, 400 mcg, 600 mcg, 800 mcg, 1000 mcg, 1200 mcg, 1400 mcg, and
1600 mcg
Professed standard
Prostacyclin (PGI
2
) receptor (IP receptor) agonist
Janssen Inc
19 Green Belt Drive
Toronto, Ontario
M3C 1L9
www.janssen.com/canada
Date of Initial Authorization:
January 20, 2016
Date of Revision:
April 21, 2022
Submission Control Number: 258347
© 2022 Janssen Inc.
All trademarks used under licence.
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_EDMS-RIM-516055 v12.0 _
_Page 2 of 37 _
RECENT MAJOR LABEL CHANGES
4 DOSAGE AND ADMINISTRATION, 4.2 Recommended Dose and Dosage
Adjustment, Dosage adjustment with co-administration of moderate
CYP2C8
inhibitors
06/2020
7 WARNINGS AND PRECAUTIONS
11/2021
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
4
DOSAGE AND ADMINISTRATION
..............................................................................
4
4.2
Recommended Dose and Dosage Adjustment
.................................................