CLOPIXOL-ACUPHASE 50MG/ML SOLUTION

Страна: Канада

Език: английски

Източник: Health Canada

Купи го сега

Активна съставка:

ZUCLOPENTHIXOL ACETATE

Предлага се от:

LUNDBECK CANADA INC

АТС код:

N05AF05

INN (Международно Name):

ZUCLOPENTHIXOL

дозиране:

50MG

Лекарствена форма:

SOLUTION

Композиция:

ZUCLOPENTHIXOL ACETATE 50MG

Начин на приложение:

INTRAMUSCULAR

Броя в опаковка:

5X1ML/5X2ML

Вид предписание :

Prescription

Терапевтична област:

THIOXANTHENES

Каталог на резюме:

Active ingredient group (AIG) number: 0127601001; AHFS:

Статус Оторизация:

APPROVED

Дата Оторизация:

1997-01-30

Данни за продукта

                                _ _
_ _
_Page 1 of 34_
PRODUCT MONOGRAPH
Pr
CLOPIXOL
®
Zuclopenthixol Tablets Lundbeck Std.
(10 mg and 25 mg zuclopenthixol as zuclopenthixol hydrochloride)
Lundbeck standard
Pr
CLOPIXOL-ACUPHASE
®
50 mg/mL Zuclopenthixol Intramuscular Injection
(45.25 mg/mL zuclopenthixol as zuclopenthixol acetate)
Lundbeck standard
Pr
CLOPIXOL
® DEPOT
200 mg/mL Zuclopenthixol Intramuscular Injection
(144.4 mg/mL zuclopenthixol as zuclopenthixol decanoate)
Lundbeck standard
ANTIPSYCHOTIC AGENT
Lundbeck Canada Inc.
1000 De la Gauchetière Street West
Suite 500
Montréal, QC
H3B 4W5
Date of Revision:
08 April 2014
Submission Control No : 171198
_ _
_ _
_Page 2 of 34_
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
....................................................................................................9
DRUG INTERACTIONS
..................................................................................................13
DOSAGE AND ADMINISTRATION
..............................................................................14
OVERDOSAGE
................................................................................................................19
ACTION AND CLINICAL PHARMACOLOGY
............................................................19
STORAGE AND STABILITY
..........................................................................................20
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................21
PART II: SCIENTIFIC INFORMATION
............................
                                
                                Прочетете целия документ
                                
                            

Документи на други езици

Данни за продукта Данни за продукта френски 08-04-2014

Сигнали за търсене, свързани с този продукт

Преглед на историята на документите