PREMPLUS CYCLE KIT

Šalis: Kanada

kalba: anglų

Šaltinis: Health Canada

Nusipirk tai dabar

Parsisiųsti Prekės savybės (SPC)
21-12-2010

Veiklioji medžiaga:

CONJUGATED ESTROGENS; MEDROXYPROGESTERONE ACETATE

Prieinama:

PFIZER CANADA ULC

ATC kodas:

G03FA12

INN (Tarptautinis Pavadinimas):

MEDROXYPROGESTERONE AND ESTROGEN

Dozė:

0.625MG; 10MG

Vaisto forma:

KIT

Sudėtis:

CONJUGATED ESTROGENS 0.625MG; MEDROXYPROGESTERONE ACETATE 10MG

Vartojimo būdas:

ORAL

Vienetai pakuotėje:

42

Recepto tipas:

Prescription

Gydymo sritis:

ESTROGENS

Produkto santrauka:

Active ingredient group (AIG) number: 0242061003; AHFS:

Autorizacija statusas:

CANCELLED PRE MARKET

Leidimo data:

2019-11-06

Prekės savybės

                                _Premplus _
®
_ and Premplus Cycle_
®
_ _
_Page 1 of 49_
PRODUCT MONOGRAPH
Pr
PREMPLUS
®
conjugated estrogens tablets CSD 0.625 mg and
medroxyprogesterone acetate tablets USP 2.5 mg, 5.0 mg
(Continuous therapy)
Pr
PREMPLUS CYCLE
®
conjugated estrogens tablets CSD 0.625 mg and
medroxyprogesterone acetate tablets USP 10.0 mg
(Cyclic therapy)
Estrogenic Hormones/Progestin
® Wyeth LLC
Pfizer Canada Inc., Licensee
17,300 Trans-Canada Highway
Kirkland, Quebec H9J 2M5
Date of Revision:
DECEMBER 8, 2010
Submission Control No: 141329
_Premplus _
®
_ and Premplus Cycle_
®
_ _
_Page 2 of 49_
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
.........................................................3
SUMMARY PRODUCT
INFORMATION...........................................................................3
INDICATIONS AND CLINICAL USE
................................................................................3
CONTRAINDICATIONS......................................................................................................4
WARNINGS AND PRECAUTIONS
....................................................................................4
ADVERSE REACTIONS
....................................................................................................14
DRUG INTERACTIONS
..................................................................................................22
DOSAGE AND ADMINISTRATION
................................................................................23
OVERDOSAGE...................................................................................................................24
ACTION AND CLINICAL
PHARMACOLOGY...............................................................25
STORAGE AND STABILITY
............................................................................................30
SPECIAL HANDLING
INSTRUCTIONS..........................................................................30
DOSAGE FORMS, COMPOSITION AND
PACKAGING................................................30
P
                                
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