TEVA-ATAZANAVIR CAPSULE

Země: Kanada

Jazyk: angličtina

Zdroj: Health Canada

Aktivní složka:

ATAZANAVIR (ATAZANAVIR SULFATE)

Dostupné s:

TEVA CANADA LIMITED

ATC kód:

J05AE08

INN (Mezinárodní Name):

ATAZANAVIR

Dávkování:

300MG

Léková forma:

CAPSULE

Složení:

ATAZANAVIR (ATAZANAVIR SULFATE) 300MG

Podání:

ORAL

Jednotky v balení:

10/30/60

Druh předpisu:

Prescription

Terapeutické oblasti:

HIV PROTEASE INHIBITORS

Přehled produktů:

Active ingredient group (AIG) number: 0149741004; AHFS:

Stav Autorizace:

APPROVED

Datum autorizace:

2017-04-18

Charakteristika produktu

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_Teva-Atazanavir _
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PRODUCT MONOGRAPH
PR
TEVA-ATAZANAVIR
Atazanavir capsules
150 mg, 200 mg and 300 mg
(as atazanavir sulfate)
Azapeptide Inhibitor of HIV-1 Protease
Teva Canada Limited
30 Novopharm Court
Toronto, Ontario
M1B 2K9
www.tevacanada.com
Date of Revision: April 12, 2021
Submission Control No: 240892
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_Teva-Atazanavir _
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TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
............................................................... 3
SUMMARY PRODUCT INFORMATION
........................................................................
3
INDICATIONS AND CLINICAL USE
.............................................................................
3
CONTRAINDICATIONS
...................................................................................................
4
WARNINGS AND PRECAUTIONS
.................................................................................
5
ADVERSE REACTIONS
.................................................................................................
12
DRUG INTERACTIONS
.................................................................................................
23
DOSAGE AND ADMINISTRATION
.............................................................................
35
OVERDOSAGE
................................................................................................................
38
ACTION AND CLINICAL PHARMACOLOGY
............................................................ 39
STORAGE AND STABILITY
.........................................................................................
43
DOSAGE FORMS, COMPOSITION AND PACKAGING
............................................. 44
PART II: SCIENTIFIC INFORMATION
....................................................................................
45
PHARMACEUTICAL INFORMATION
.........................................................................
45
CLINICAL TRIALS
......................................................................................................