TORRENT-OLANZAPINE ODT TABLET (ORALLY DISINTEGRATING)

Ország: Kanada

Nyelv: angol

Forrás: Health Canada

Vedd Meg Most

Termékjellemzők Termékjellemzők (SPC)
21-02-2014

Aktív összetevők:

OLANZAPINE

Beszerezhető a:

TORRENT PHARMACEUTICALS LIMITED

ATC-kód:

N05AH03

INN (nemzetközi neve):

OLANZAPINE

Adagolás:

10MG

Gyógyszerészeti forma:

TABLET (ORALLY DISINTEGRATING)

Összetétel:

OLANZAPINE 10MG

Az alkalmazás módja:

ORAL

db csomag:

100

Recept típusa:

Prescription

Terápiás terület:

ATYPICAL ANTIPSYCHOTICS

Termék összefoglaló:

Active ingredient group (AIG) number: 0128783002; AHFS:

Engedélyezési státusz:

CANCELLED (UNRETURNED ANNUAL)

Engedély dátuma:

2021-12-20

Termékjellemzők

                                _ _
_ _
_Page 1 of 62_
PRODUCT MONOGRAPH
PR
TORRENT-OLANZAPINE ODT
Olanzapine
Orally Disintegrating Tablets
5 mg, 10 mg, 15 mg, 20 mg
Antipsychotic Agent
Torrent Pharmaceuticals Ltd.
Ahmedabad-Mehsana Highway
Taluka - Kadi, Dist. Mehsana
Indrad-382 721, Gujarat, India
Distributed by:
Torrent Pharma Canada Inc.
Woodbridge, ON, L4H 1Y6
Date of Revision :
February 07, 2014
Submission Control No: 166045
_ _
_ _
_Page 2 of 62_
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
.........................................................3
SUMMARY PRODUCT INFORMATION
........................................................................3
INDICATIONS AND CLINICAL USE
..............................................................................3
CONTRAINDICATIONS
...................................................................................................4
WARNINGS AND PRECAUTIONS
..................................................................................4
ADVERSE REACTIONS
..................................................................................................13
DRUG INTERACTIONS
..................................................................................................27
DOSAGE AND ADMINISTRATION
..............................................................................29
OVERDOSAGE
................................................................................................................31
ACTION AND CLINICAL PHARMACOLOGY
............................................................32
STORAGE AND STABILITY
..........................................................................................34
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................34
PART II: SCIENTIFIC INFORMATION
...............................................................................36
PHARMACEUTICAL INFORMATION
..........................................................................36
CLINICAL TRIALS
..............................................................
                                
                                Olvassa el a teljes dokumentumot
                                
                            

A termékkel kapcsolatos riasztások keresése