GALANTAMINE ER CAPSULE (EXTENDED RELEASE)

Land: Kanada

Språk: engelska

Källa: Health Canada

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Produktens egenskaper Produktens egenskaper (SPC)
23-06-2017

Aktiva substanser:

GALANTAMINE (GALANTAMINE HYDROBROMIDE)

Tillgänglig från:

SANIS HEALTH INC

ATC-kod:

N06DA04

INN (International namn):

GALANTAMINE

Dos:

8MG

Läkemedelsform:

CAPSULE (EXTENDED RELEASE)

Sammansättning:

GALANTAMINE (GALANTAMINE HYDROBROMIDE) 8MG

Administreringssätt:

ORAL

Enheter i paketet:

100

Receptbelagda typ:

Prescription

Terapiområde:

PARASYMPATHOMEMETIC (CHOLINERGIC) AGENTS

Produktsammanfattning:

Active ingredient group (AIG) number: 0144660002; AHFS:

Bemyndigande status:

APPROVED

Tillstånd datum:

2016-01-07

Produktens egenskaper

                                Page 1 of 55
PRODUCT MONOGRAPH
PR
GALANTAMINE ER
Galantamine Hydrobromide Extended-Release Capsules
8 mg, 16 mg, 24 mg galantamine base
Cholinesterase Inhibitor
SANIS HEALTH INC.
1 President's Choice Circle
Brampton, Ontario
L6Y 5S5
Date of Revision: June 22, 2017
Submission Control No: 206599
Page 2 of 55
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
...................................................................................................
8
DRUG INTERACTIONS
.................................................................................................
14
DOSAGE AND ADMINISTRATION
.............................................................................
16
OVERDOSAGE
...............................................................................................................
17
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
..............................................
                                
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