SANDOZ ESTRADIOL DERM 100 PATCH

Land: Kanada

Tungumál: enska

Heimild: Health Canada

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Download Vara einkenni (SPC)
25-03-2009

Virkt innihaldsefni:

ESTRADIOL (ESTRADIOL HEMIHYDRATE)

Fáanlegur frá:

SANDOZ CANADA INCORPORATED

ATC númer:

G03CA03

INN (Alþjóðlegt nafn):

ESTRADIOL

Skammtar:

100MCG

Lyfjaform:

PATCH

Samsetning:

ESTRADIOL (ESTRADIOL HEMIHYDRATE) 100MCG

Stjórnsýsluleið:

TRANSDERMAL

Einingar í pakka:

8

Gerð lyfseðils:

Prescription

Lækningarsvæði:

ESTROGENS

Vörulýsing:

Active ingredient group (AIG) number: 0106457037; AHFS:

Leyfisstaða:

APPROVED

Leyfisdagur:

2006-01-11

Vara einkenni

                                PRODUCT MONOGRAPH
SANDOZ ESTRADIOL DERM 50, 75 AND 100 ESTRADIOL HEMIHYDRATE (ESTRADIOL-17Β)
TRANSDERMAL THERAPEUTIC SYSTEM
4, 6 AND 8 MG ESTRADIOL PATCHES
CORRESPONDING TO
50 MCG/DAY, 75 MCG/DAY AND 100 MCG/DAY DELIVERY
ESTROGEN
Sandoz Canada Inc.
145 Jules-Léger
Date of Revision: March 19, 2009
Boucherville, QC, Canada
J4B 7K8
CONTROL NUMBER: 120474
_ _
_Sandoz Estradiol Derm _
_Page 2 of 34 _
_ _
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........................................................................................................................................
11
DRUG
INTERACTIONS
........................................................................................................................................
12
DOSAGE
AND
ADMINISTRATION
....................................................................................................................
14
OVERDOSAGE
......................................................................................................................................................
16
ACTIONS
AND
CLINICAL
PHARMACOLOGY.................................................................................................
16
STORAGE
AND
STABILITY
.....................................................................................................................
                                
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