ODEFSEY TABLET

Šalis: Kanada

kalba: anglų

Šaltinis: Health Canada

Nusipirk tai dabar

Prekės savybės Prekės savybės (SPC)
13-11-2019

Veiklioji medžiaga:

EMTRICITABINE; RILPIVIRINE (RILPIVIRINE HYDROCHLORIDE); TENOFOVIR ALAFENAMIDE (TENOFOVIR ALAFENAMIDE HEMIFUMARATE)

Prieinama:

GILEAD SCIENCES CANADA INC

ATC kodas:

J05AR19

INN (Tarptautinis Pavadinimas):

EMTRICITABINE, TENOFOVIR ALAFENAMIDE AND RILPIVIRINE

Dozė:

200MG; 25MG; 25MG

Vaisto forma:

TABLET

Sudėtis:

EMTRICITABINE 200MG; RILPIVIRINE (RILPIVIRINE HYDROCHLORIDE) 25MG; TENOFOVIR ALAFENAMIDE (TENOFOVIR ALAFENAMIDE HEMIFUMARATE) 25MG

Vartojimo būdas:

ORAL

Vienetai pakuotėje:

30

Recepto tipas:

Prescription

Gydymo sritis:

NONNUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS

Produkto santrauka:

Active ingredient group (AIG) number: 0358830001; AHFS:

Autorizacija statusas:

APPROVED

Leidimo data:

2017-02-10

Prekės savybės

                                PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
ODEFSEY
®
(EMTRICITABINE/RILPIVIRINE/TENOFOVIR ALAFENAMIDE) TABLETS
200 mg emtricitabine
25 mg rilpivirine (as rilpivirine hydrochloride)
25 mg tenofovir alafenamide (as tenofovir alafenamide hemifumarate)
ANTIRETROVIRAL AGENT
Gilead Sciences Canada, Inc.
Mississauga, ON L5N 2W3
www.gilead.ca
Submission Control No: 229507
Date of Initial Approval:
February 10, 2017
Date of Revision:
November 13, 2019
ODEFSEY (emtricitabine/rilpivirine*/tenofovir alafenamide**) tablets
*as rilpivirine hydrochloride **as tenofovir alafenamide hemifumarate
Product Monograph
_ _
_ _
_Page 2 of 97_
RECENT MAJOR LABEL CHANGES
Serious Warnings and Precautions Box (3)
06/2018
Dosage and Administration, Dosing Considerations (4.1)
10/2019
Dosage and Administration, Recommended Dose and Dose Adjustment (4.2)
12/2018
Warnings and Precautions, General (7)
10/2019
Warnings and Precautions, Cardiovascular (7)
10/2019
Warnings and Precautions, Serum Lipids and Blood Glucose (7)
06/2018
Warnings and Precautions, Gastrointestinal (7)
01/2018
Warnings and Precautions, Lactic Acidosis/Severe Hepatomegaly with
Steatosis
(7)
06/2018
Warnings and Precautions, Musculoskeletal (7)
06/2018
Warnings and Precautions, Renal (7)
10/2019
Warnings and Precautions, Risk of Adverse Reactions or Loss of
Virologic
Response Due to Drug Interactions (7)
10/2019
Warnings and Precautions, Special Populations, Pregnant Women (7.1.2)
12/2018
TABLE OF CONTENTS
RECENT MAJOR LABEL CHANGES
...........................................................................................................
2
TABLE OF CONTENTS
................................................................................................................................
2
PART I: HEALTH PROFESSIONAL INFORMATION
...................................................................................
4
1.
INDICATIONS
....................................................................................................................................
                                
                                Perskaitykite visą dokumentą
                                
                            

Dokumentai kitomis kalbomis

Prekės savybės Prekės savybės prancūzų 13-11-2019

Peržiūrėti dokumentų istoriją