ALLERNIX MULTI SYMPTOM TABLET

Country: কানাডা

ভাষা: ইংরেজি

সূত্র: Health Canada

সক্রিয় উপাদান:

DESLORATADINE

থেকে পাওয়া:

TEVA CANADA LIMITED

এটিসি কোড:

R06AX27

INN (International Name):

DESLORATADINE

ডোজ:

5MG

ফার্মাসিউটিকাল ফর্ম:

TABLET

রচনা:

DESLORATADINE 5MG

প্রশাসন রুট:

ORAL

প্যাকেজ ইউনিট:

10

প্রেসক্রিপশন টাইপ:

OTC

Therapeutic area:

SECOND GENERATION ANTIHISTAMINES

পণ্য সারাংশ:

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

অনুমোদন অবস্থা:

CANCELLED POST MARKET

অনুমোদন তারিখ:

2020-05-11

পণ্য বৈশিষ্ট্য

_ _
_ALLERNIX MULTI SYMPTOM _
_Page 1 of 36_
PRODUCT MONOGRAPH
ALLERNIX MULTI SYMPTOM
Desloratadine Tablets
5 mg
HISTAMINE H
1
-RECEPTOR ANTAGONIST
Teva Canada Limited
30 Novopharm Court
Toronto, Ontario
Canada M1B 2K9
www.tevacanada.com
Date of Preparation:
April 3, 2013
Submission Control No: 163170
_ _
_ALLERNIX MULTI SYMPTOM _
_Page 2 of 36_
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
...............................................................................
7
OVERDOSAGE
.................................................................................................................
7
ACTION AND CLINICAL PHARMACOLOGY
............................................................. 7
STORAGE AND STABILITY
.........................................................................................
10
DOSAGE FORMS, COMPOSITION AND PACKAGING
............................................ 11
PART II: SCIENTIFIC INFORMATION
..............................................................................
12
PHARMACEUTICAL INFORMATION
.........................................................................
12
CLINICAL TRIALS
.........................................................................................................
13
DETAILED PHARMACOLOGY
....