TARO-CYPROTERONE/ETHINYL ESTRADIOL TABLET

Land: Kanada

Sprache: Englisch

Quelle: Health Canada

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05-08-2020

Wirkstoff:

CYPROTERONE ACETATE; ETHINYL ESTRADIOL

Verfügbar ab:

SUN PHARMA CANADA INC

ATC-Code:

G03HB01

INN (Internationale Bezeichnung):

CYPROTERONE AND ESTROGEN

Dosierung:

2MG; 0.035MG

Darreichungsform:

TABLET

Zusammensetzung:

CYPROTERONE ACETATE 2MG; ETHINYL ESTRADIOL 0.035MG

Verabreichungsweg:

ORAL

Einheiten im Paket:

21+7

Verschreibungstyp:

Prescription

Therapiebereich:

OTHER MISCELLANEOUS THERAPEUTIC AGENTS

Produktbesonderheiten:

Active ingredient group (AIG) number: 0232337001; AHFS:

Berechtigungsstatus:

APPROVED

Berechtigungsdatum:

2020-08-05

Fachinformation

                                _Pr_
_TARO-CYPROTERONE/ETHINYL ESTRADIOL (CYPROTERONE ACETATE AND ETHINYL
ESTRADIOL TABLETS) PRODUCT MONOGRAPH _
_Page 1 of 47 _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
TARO-CYPROTERONE/ETHINYL ESTRADIOL
2 mg cyproterone acetate and 0.035 mg ethinyl estradiol tablets
Acne Therapy
Sun Pharma Canada Inc.
Date of Revision:
126 East Drive
August 5, 2020
Brampton, Ontario
L6T 1C1
Submission Control No.: 240914
_Pr_
_TARO-CYPROTERONE/ETHINYL ESTRADIOL (CYPROTERONE ACETATE AND ETHINYL
ESTRADIOL TABLETS) PRODUCT MONOGRAPH _
_Page 2 of 47 _
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
.........................................................................................................................
12
DRUG INTERACTIONS
.........................................................................................................................
15
DOSAGE AND ADMINISTRATION
.....................................................................................................
19
OVERDOSAGE
.......................................................................................................................................
21
ACTION AND CLINICAL PHARMACOLOGY
....................................................................................
21
STORAGE AND STABILITY
.................................................................................................................
                                
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