PREZCOBIX TABLET

Pajjiż: Kanada

Lingwa: Ingliż

Sors: Health Canada

Ixtrih issa

Ingredjent attiv:

DARUNAVIR (DARUNAVIR ETHANOLATE); COBICISTAT

Disponibbli minn:

JANSSEN INC

Kodiċi ATC:

J05AR14

INN (Isem Internazzjonali):

DARUNAVIR AND COBICISTAT

Dożaġġ:

800MG; 150MG

Għamla farmaċewtika:

TABLET

Kompożizzjoni:

DARUNAVIR (DARUNAVIR ETHANOLATE) 800MG; COBICISTAT 150MG

Rotta amministrattiva:

ORAL

Unitajiet fil-pakkett:

30

Tip ta 'preskrizzjoni:

Prescription

Żona terapewtika:

HIV PROTEASE INHIBITORS

Sommarju tal-prodott:

Active ingredient group (AIG) number: 0255810001; AHFS:

L-istatus ta 'awtorizzazzjoni:

APPROVED

Data ta 'l-awtorizzazzjoni:

2014-06-19

Karatteristiċi tal-prodott

                                Non Ann PM PRCB SNDS 268359 02222023.docx
EDMS-ERI-840430 V8.0_ _
_Page 1 of 65_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
PREZCOBIX
®
darunavir (as darunavir ethanolate)/cobicistat
film-coated tablets (800 mg/150 mg)
Human Immunodeficiency Virus (HIV) Protease Inhibitor
Janssen Inc.
19 Green Belt Drive
Toronto, Ontario
M3C 1L9
www.janssen.com/canada
Date of Initial Authorization:
June 18, 2014
Date of Revision:
March 3, 2023
Submission Control Number: 268359
© 2023 Janssen Inc.
All trademarks used under license.
Non Ann PM PRCB SNDS 268359 02222023.docx
EDMS-ERI-840430 V8.0_ _
_Page 2 of 65_
RECENT MAJOR LABEL CHANGES
2 CONTRAINDICATIONS
08/2022
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 .......................................................................
5
4.1
Dosing Considerations
.......................................................................................
5
4.2
Recommended Dose and Dosage Adjustment
.............................................. 5
4.4
Administration
......................................................................................................
7
4.5
Missed 
                                
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