FIRMAGON POWDER FOR SOLUTION

Ülke: Kanada

Dil: İngilizce

Kaynak: Health Canada

Aktif bileşen:

DEGARELIX (DEGARELIX ACETATE)

Mevcut itibaren:

FERRING INC

ATC kodu:

L02BX02

INN (International Adı):

DEGARELIX

Doz:

80MG

Farmasötik formu:

POWDER FOR SOLUTION

Kompozisyon:

DEGARELIX (DEGARELIX ACETATE) 80MG

Uygulama yolu:

SUBCUTANEOUS

Paketteki üniteler:

80MG

Reçete türü:

Prescription

Terapötik alanı:

ANTINEOPLASTIC AGENTS

Ürün özeti:

Active ingredient group (AIG) number: 0152667001; AHFS:

Yetkilendirme durumu:

APPROVED

Yetkilendirme tarihi:

2009-11-16

Ürün özellikleri

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PRODUCT MONOGRAPH
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FIRMAGON
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Degarelix for Injection
120 mg degarelix (as degarelix acetate) per vial
80 mg degarelix (as degarelix acetate) per vial
Gonadotropin-Releasing Hormone Receptor Antagonist
Ferring Pharmaceuticals
200 Yorkland Blvd., Suite 500
North York, Ontario
M2J 5C1
DATE OF REVISION:
March 18, 2016
SUBMISSION CONTROL NO: 180927
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_FIRMAGON_
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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
....................................................................................................8
DRUG INTERACTIONS
..................................................................................................11
DOSAGE AND ADMINISTRATION
..............................................................................12
OVERDOSAGE
................................................................................................................26
ACTION AND CLINICAL PHARMACOLOGY
............................................................26
STORAGE AND STABILITY
..........................................................................................30
SPECIAL HANDLING INSTRUCTIONS
.......................................................................30
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................30
PART II: SCIENTIFIC INFORMATION
...............................................................................31
PHARMACEUTICAL INFORMATION
............................................