DESLORATADINE ALLERGY CONTROL TABLET

Država: Kanada

Jezik: angleščina

Source: Health Canada

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Prenos Lastnosti izdelka (SPC)
12-09-2023

Aktivna sestavina:

DESLORATADINE

Dostopno od:

PHARMASCIENCE INC

Koda artikla:

R06AX27

INN (mednarodno ime):

DESLORATADINE

Odmerek:

5MG

Farmacevtska oblika:

TABLET

Sestava:

DESLORATADINE 5MG

Pot uporabe:

ORAL

Enote v paketu:

10/20/30/50

Tip zastaranja:

OTC

Terapevtsko območje:

SECOND GENERATION ANTIHISTAMINES

Povzetek izdelek:

Active ingredient group (AIG) number: 0143961001; AHFS:

Status dovoljenje:

APPROVED

Datum dovoljenje:

2009-11-06

Lastnosti izdelka

                                _DESLORATADINE ALLERGY _CONTROL page 1 of 37
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
DESLORATADINE ALLERGY CONTROL
Desloratadine
Tablet, 5mg, Oral
House Standard
Histamine H1-Receptor Antagonist
PHARMASCIENCE INC.
6111 Royalmount Avenue, Suite 100
Montréal, Canada
H4P 2T4
Date of initial Authorization:
SEP 22, 2011
Date of Revision:
SEP 12, 2023
Submission Control Number: 272961
_DESLORATADINE ALLERGY _CONTROL page 2 of 37
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
...................................................................................
4
1
INDICATIONS
....................................................................................................................................
4
1.1
PEDIATRICS
....................................................................................................................................
4
1.2
GERIATRICS
....................................................................................................................................
4
2
CONTRAINDICATIONS
.......................................................................................................................
4
3
SERIOUS WARNINGS AND PRECAUTIONS BOX
..................................................................................
4
4
DOSAGE AND ADMINISTRATION
.......................................................................................................
4
4.1
DOSING CONSIDERATIONS
................................................................................................................
4
4.2
RECOMMENDED DOSE AND DOSAGE ADJUSTMENT
.............................................................................
5
4.3
ADMINISTRATION
............................................................................................................................
5
4.4
MISSED DOSE
................................................................................................................................
5
5
OVERDOSAGE
......................................
                                
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