AERIUS SYRUP

Država: Kanada

Jezik: angleščina

Source: Health Canada

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Lastnosti izdelka Lastnosti izdelka (SPC)
04-12-2014

Aktivna sestavina:

DESLORATADINE

Dostopno od:

BAYER INC

Koda artikla:

R06AX27

INN (mednarodno ime):

DESLORATADINE

Odmerek:

0.5MG

Farmacevtska oblika:

SYRUP

Sestava:

DESLORATADINE 0.5MG

Pot uporabe:

ORAL

Enote v paketu:

100

Tip zastaranja:

OTC

Terapevtsko območje:

SECOND GENERATION ANTIHISTAMINES

Povzetek izdelek:

Active ingredient group (AIG) number: 0143961002; AHFS:

Status dovoljenje:

APPROVED

Datum dovoljenje:

2014-12-18

Lastnosti izdelka

                                _AERIUS Tablets / AERIUS Syrup / AERIUS KIDS Syrup _
_Page 1 of 37 _
PRODUCT MONOGRAPH
AERIUS
®
DESLORATADINE TABLET 5 MG
DESLORATADINE SYRUP 0.5 MG/ML
AERIUS KIDS
®
DESLORATADINE SYRUP 0.5 MG/ML
HISTAMINE H
1
-RECEPTOR ANTAGONIST
Bayer Inc., Consumer Care
2920 Matheson Blvd. E
Mississauga, ON
L4W 5R6
Date of Preparation:
December 4, 2014
Submission Control No: 179382, 179387
_AERIUS Tablets / AERIUS Syrup / AERIUS KIDS Syrup _
_Page 2 of 37 _
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
....................................................................................................5
DRUG INTERACTIONS
....................................................................................................7
DOSAGE AND ADMINISTRATION
................................................................................7
OVERDOSAGE
..................................................................................................................8
ACTION AND CLINICAL PHARMACOLOGY
..............................................................8
STORAGE AND STABILITY
..........................................................................................11
SPECIAL HANDLING INSTRUCTIONS
.......................................................................11
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................11
PART II: SCIENTIFIC INFORMATION
...............................................................................13
PHARMACEUTICAL INFORMATION
......................
                                
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