TEVA-GALANTAMINE ER CAPSULE (EXTENDED RELEASE)

Country: Kanada

Bahasa: Inggeris

Sumber: Health Canada

Bahan aktif:

GALANTAMINE (GALANTAMINE HYDROBROMIDE)

Boleh didapati daripada:

TEVA CANADA LIMITED

Kod ATC:

N06DA04

INN (Nama Antarabangsa):

GALANTAMINE

Dos:

24MG

Borang farmaseutikal:

CAPSULE (EXTENDED RELEASE)

Komposisi:

GALANTAMINE (GALANTAMINE HYDROBROMIDE) 24MG

Laluan pentadbiran:

ORAL

Unit dalam pakej:

30/100

Jenis preskripsi:

Prescription

Kawasan terapeutik:

PARASYMPATHOMEMETIC (CHOLINERGIC) AGENTS

Ringkasan produk:

Active ingredient group (AIG) number: 0144660005; AHFS:

Status kebenaran:

CANCELLED POST MARKET

Tarikh kebenaran:

2018-06-22

Ciri produk

_TEVA-GALANTAMINE _
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PRODUCT MONOGRAPH
PR
TEVA-GALANTAMINE ER
galantamine hydrobromide extended release capsules
8 mg, 16 mg, 24 mg galantamine base
Cholinesterase Inhibitor
Teva Canada Limited
Date of Revision:
30 Novopharm Court
September 3, 2014
Toronto, Ontario
M1B 2K9
Submission Control No: 177342
_TEVA-GALANTAMINE _
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_Page 2 of 55 _
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
......................................................... 3
SUMMARY PRODUCT INFORMATION
.......................................................................
3
INDICATIONS AND CLINICAL USE
.............................................................................
3
WARNINGS AND PRECAUTIONS
.................................................................................
4
ADVERSE REACTIONS
...................................................................................................
8
DRUG INTERACTIONS
.................................................................................................
14
DOSAGE AND ADMINISTRATION
.............................................................................
16
OVERDOSAGE
...............................................................................................................
18
ACTION AND CLINICAL PHARMACOLOGY
........................................................... 19
STORAGE AND STABILITY
.........................................................................................
23
DOSAGE FORMS, COMPOSITION AND PACKAGING
............................................ 23
PART II: SCIENTIFIC INFORMATION
...............................................................................
25
PHARMACEUTICAL INFORMATION
.........................................................................
25
CLINICAL TRIALS
.........................................................................................................
26
DETAILED PHARMACOLOGY
....................................................................................
35
TOXICOLOGY
...........