PATANOL SOLUTION

Pays: Canada

Langue: anglais

Source: Health Canada

Ingrédients actifs:

OLOPATADINE (OLOPATADINE HYDROCHLORIDE)

Disponible depuis:

NOVARTIS PHARMACEUTICALS CANADA INC

Code ATC:

S01GX09

DCI (Dénomination commune internationale):

OLOPATADINE

Dosage:

0.1%

forme pharmaceutique:

SOLUTION

Composition:

OLOPATADINE (OLOPATADINE HYDROCHLORIDE) 0.1%

Mode d'administration:

OPHTHALMIC

Unités en paquet:

5ML/10ML/15ML

Type d'ordonnance:

Prescription

Domaine thérapeutique:

ANTIHISTAMINE DRUGS

Descriptif du produit:

Active ingredient group (AIG) number: 0132394001; AHFS:

Statut de autorisation:

APPROVED

Date de l'autorisation:

2017-02-02

Résumé des caractéristiques du produit

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_PATANOL_
_®_
_ Product Monograph _
_Page 1 of 19 _
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PRODUCT MONOGRAPH
PR
PATANOL
®
Olopatadine Hydrochloride Ophthalmic Solution
0.1% w/v olopatadine (as olopatadine hydrochloride)
Anti-allergy Agent
Novartis Pharmaceuticals Canada Inc.
385 Bouchard Blvd.
Dorval, Quebec
Canada H9S 1A9
www.novartis.ca
Date of Revision:
March 2, 2018
Control Number: 211652
PATANOL and DROP-TAINER are registered trademarks.
*All trademarks and registered trademarks are the property of their
respective owners.
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_PATANOL_
_®_
_ Product Monograph _
_Page 2 of 19 _
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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
..................................................................................3
ADVERSE REACTIONS
....................................................................................................5
DRUG INTERACTIONS
....................................................................................................6
DOSAGE AND ADMINISTRATION
................................................................................6
OVERDOSAGE
..................................................................................................................6
ACTION AND CLINICAL PHARMACOLOGY
..............................................................6
STORAGE AND STABILITY
............................................................................................8
DOSAGE FORMS, COMPOSITION AND PACKAGING
...............................................8
PART II: SCIENTIFIC INFORMATION
.................................................................................9
PHARMACEUTICAL INFORMATION
...