CYESTRA-35 TABLET

Страна: Канада

Език: английски

Източник: Health Canada

Активна съставка:

CYPROTERONE ACETATE; ETHINYL ESTRADIOL

Предлага се от:

PALADIN LABS INC.

АТС код:

G03HB01

INN (Международно Name):

CYPROTERONE AND ESTROGEN

дозиране:

2MG; 0.035MG

Лекарствена форма:

TABLET

Композиция:

CYPROTERONE ACETATE 2MG; ETHINYL ESTRADIOL 0.035MG

Начин на приложение:

ORAL

Броя в опаковка:

21

Вид предписание :

Prescription

Терапевтична област:

OTHER MISCELLANEOUS THERAPEUTIC AGENTS

Каталог на резюме:

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

Статус Оторизация:

APPROVED

Дата Оторизация:

2007-03-01

Данни за продукта

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_CYESTRA-35 Product Monograph Page 1 of 48 _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
CYESTRA
®
-35
cyproterone acetate and ethinyl estradiol tablets
2 mg/0.035 mg
THERAPEUTIC CLASSIFICATION
Acne Therapy
Paladin Labs Inc.
Date of Preparation:
100 Alexis Nihon Blvd, Suite 600
January 17, 2019
St-Laurent, Quebec
Version: 6.0
H4M 2P2
Control # 223341
______________________________________________________________________________________________
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_CYESTRA-35 Product Monograph Page 2 of 48 _
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
..................................................................3
SUMMARY PRODUCT INFORMATION
......................................................................................3
INDICATION AND CLINICAL USE
..............................................................................................3
CONTRAINDICATIONS
...............................................................................................................3
WARNINGS AND PRECAUTIONS
...............................................................................................4
ADVERSE
REACTIONS..............................................................................................................
13
DRUG INTERACTIONS
..............................................................................................................
16
DOSAGE AND
ADMINISTRATION
.........................................................................................
20
OVERDOSAGE
...........................................................................................................................
22
ACTION AND CLINICAL PHARMACOLOGY
...........................................................................
22
STORAGE AND STABILITY
......................................................................................................
24
SPECIAL HANDLING INSTRUCTIONS
............................