AGENERASE LIQUID

Maa: Kanada

Kieli: englanti

Lähde: Health Canada

Aktiivinen ainesosa:

AMPRENAVIR

Saatavilla:

GLAXOSMITHKLINE INC

ATC-koodi:

J05AE05

INN (Kansainvälinen yleisnimi):

AMPRENAVIR

Annos:

15MG

Lääkemuoto:

LIQUID

Koostumus:

AMPRENAVIR 15MG

Antoreitti:

ORAL

Kpl paketissa:

240 ML

Prescription tyyppi:

Prescription

Terapeuttinen alue:

HIV PROTEASE INHIBITORS

Tuoteyhteenveto:

Active ingredient group (AIG) number: 0143241003; AHFS:

Valtuutuksen tilan:

CANCELLED POST MARKET

Valtuutus päivämäärä:

2008-05-27

Valmisteyhteenveto

_DCTM/498/510/131-2005-06-21-pm-pristine-agenerase-oral-solution.doc _
_ _
_Appendix E - Product Monograph Template - Standard _
_Page 1 of 33_
PRODUCT MONOGRAPH
Pr
AGENERASE™
amprenavir
15 mg/mL oral solution
Antiretroviral Agent
GlaxoSmithKline Inc.
7333 Mississauga Road
Mississauga, Ontario
L5N 6L4
Date of Preparation:
October 30, 2001
Date of Revision:
June 27, 2005
Submission Control No: 097413
_©_
_ 2005 GlaxoSmithKline Inc. All Rights Reserved _
_™ AGENERASE used under license by GlaxoSmithKline Inc_
_._
_Appendix E - Product Monograph Template - Standard _
_Page 2 of 33_
Table of Contents
PART I: HEALTH PROFESSIONAL
INFORMATION.........................................................3
SUMMARY PRODUCT INFORMATION
........................................................................3
INDICATIONS AND CLINICAL
USE..............................................................................3
CONTRAINDICATIONS
...................................................................................................3
WARNINGS AND
PRECAUTIONS..................................................................................4
ADVERSE
REACTIONS..................................................................................................10
DRUG INTERACTIONS
..................................................................................................12
DOSAGE AND
ADMINISTRATION..............................................................................17
OVERDOSAGE
................................................................................................................19
ACTION AND CLINICAL PHARMACOLOGY
............................................................19
STORAGE AND
STABILITY..........................................................................................22
SPECIAL HANDLING INSTRUCTIONS
.......................................................................22
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................22
PART II: SCIENTIFIC INFORMATION
.