DORZOLAMIDE-TIMOLOL SOLUTION

Riik: Kanada

keel: inglise

Allikas: Health Canada

Toimeaine:

DORZOLAMIDE (DORZOLAMIDE HYDROCHLORIDE); TIMOLOL (TIMOLOL MALEATE)

Saadav alates:

ALCON CANADA INC

ATC kood:

S01ED51

INN (Rahvusvaheline Nimetus):

TIMOLOL, COMBINATIONS

Annus:

2.0%; 0.5%

Ravimvorm:

SOLUTION

Koostis:

DORZOLAMIDE (DORZOLAMIDE HYDROCHLORIDE) 2.0%; TIMOLOL (TIMOLOL MALEATE) 0.5%

Manustamisviis:

OPHTHALMIC

Ühikuid pakis:

5ML/10ML

Retsepti tüüp:

Prescription

Terapeutiline ala:

BETA-ADRENERGIC AGENTS

Toote kokkuvõte:

Active ingredient group (AIG) number: 0237301001; AHFS:

Volitamisolek:

CANCELLED PRE MARKET

Loa andmise kuupäev:

2021-06-25

Toote omadused

_Product Monograph – _
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_Page 1 of 28_
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_DORZOLAMIDE-TIMOLOL _
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PRODUCT MONOGRAPH
PR
DORZOLAMIDE-TIMOLOL
Dorzolamide (as Dorzolamide Hydrochloride USP) 2.0% and
Timolol (as Timolol Maleate USP) 0.5% w/v
Sterile Ophthalmic Solution
Elevated Intraocular Pressure Therapy
(Topical Carbonic Anhydrase Inhibitor and Topical Beta-Adrenergic
Blocking Agent)
Alcon Canada Inc.
2665 Meadowpine Blvd.
Mississauga, ON
L5N 8C7
Date of Preparation:
October 1, 2010
SUBMISSION CONTROL NO: 131041
_Product Monograph – _
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_Page 2 of 28_
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_DORZOLAMIDE-TIMOLOL _
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TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL
INFORMATION..................................................... 3
SUMMARY PRODUCT
INFORMATION.........................................................................
3
INDICATIONS AND CLINICAL
USE...............................................................................
3
CONTRAINDICATIONS
.....................................................................................................
3
WARNINGS AND PRECAUTIONS
...................................................................................
4
ADVERSE
REACTIONS......................................................................................................
7
DRUG
INTERACTIONS......................................................................................................
8
DOSAGE AND ADMINISTRATION
...............................................................................
10
OVERDOSAGE
...................................................................................................................
10
ACTION AND CLINICAL PHARMACOLOGY
............................................................ 11
STORAGE AND
STABILITY............................................................................................
13
DOSAGE FORMS, COMPOSITION AND PACKAGING
............................................ 14
PART II: SCIENTIFIC INFORMATION
...........................................................................
15
PHARMACEUTICAL
INFORMATIO