CIPRODEX SUSPENSION

Ülke: Kanada

Dil: İngilizce

Kaynak: Health Canada

Aktif bileşen:

CIPROFLOXACIN (CIPROFLOXACIN HYDROCHLORIDE); DEXAMETHASONE

Mevcut itibaren:

NOVARTIS PHARMACEUTICALS CANADA INC

ATC kodu:

S02CA06

INN (International Adı):

DEXAMETHASONE AND ANTIINFECTIVES

Doz:

0.3%; 0.1%

Farmasötik formu:

SUSPENSION

Kompozisyon:

CIPROFLOXACIN (CIPROFLOXACIN HYDROCHLORIDE) 0.3%; DEXAMETHASONE 0.1%

Uygulama yolu:

OTIC

Paketteki üniteler:

7.5ML

Reçete türü:

Prescription

Terapötik alanı:

ANTIBACTERIALS

Ürün özeti:

Active ingredient group (AIG) number: 0250083001; AHFS:

Yetkilendirme durumu:

APPROVED

Yetkilendirme tarihi:

2004-05-10

Ürün özellikleri

_CIPRODEX_
_®_
_ Product Monograph _
_Page 1 of 20_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
Pr
CIPRODEX
®
Ciprofloxacin / Dexamethasone Otic Suspension
0.3% w/v (as ciprofloxacin hydrochloride) / 0.1% w/v
Antibacterial - Corticosteroid (Otic)
Novartis Pharmaceuticals Canada Inc.
385 Bouchard Blvd.
Dorval, Quebec
H9S 1A9
Date of Revision:
www.novartis.ca
September 27, 2017
Submission Control No.: 206140
CIPRODEX
®
is a registered trademark of Bayer, used with permission.
_CIPRODEX_
_®_
_ Product Monograph _
_Page 2 of 20_
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
....................................................................................................6
DRUG INTERACTIONS
....................................................................................................8
DOSAGE AND ADMINISTRATION
................................................................................8
OVERDOSAGE
..................................................................................................................8
ACTION AND CLINICAL PHARMACOLOGY
..............................................................9
STORAGE AND STABILITY
............................................................................................9
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................10
PART II: SCIENTIFIC INFORMATION
................................................................................11
PHARMACEUTICAL INFORMATION
.......................