MAR-GALANTAMINE ER CAPSULE (EXTENDED RELEASE)

Riik: Kanada

keel: inglise

Allikas: Health Canada

Osta kohe

Laadi alla Toote omadused (SPC)
15-01-2018

Toimeaine:

GALANTAMINE (GALANTAMINE HYDROBROMIDE)

Saadav alates:

MARCAN PHARMACEUTICALS INC

ATC kood:

N06DA04

INN (Rahvusvaheline Nimetus):

GALANTAMINE

Annus:

24MG

Ravimvorm:

CAPSULE (EXTENDED RELEASE)

Koostis:

GALANTAMINE (GALANTAMINE HYDROBROMIDE) 24MG

Manustamisviis:

ORAL

Ühikuid pakis:

30

Retsepti tüüp:

Prescription

Terapeutiline ala:

PARASYMPATHOMEMETIC (CHOLINERGIC) AGENTS

Toote kokkuvõte:

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

Volitamisolek:

CANCELLED POST MARKET

Loa andmise kuupäev:

2021-05-10

Toote omadused

                                1
PRODUCT MONOGRAPH
PR
MAR-GALANTAMINE ER
galantamine hydrobromide extended release capsules
8 mg, 16 mg, 24 mg galantamine base
Cholinesterase Inhibitor
Marcan Pharmaceuticals Inc.
Date of Revision:
77 Auriga Drive, Unit# 4
January 15, 2018
Ottawa, ON, CANADA
K2E 7Z7
Control No.: 212078
2
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
............................................................................................................................
7
DRUG INTERACTIONS
...........................................................................................................................
12
DOSAGE AND ADMINISTRATION
......................................................................................................
14
OVERDOSAGE
.........................................................................................................................................
15
ACTION AND CLINICAL PHARMACOLOGY
.....................................................................................
16
STORAGE AND STABILITY
..................................................................................................................
20
DOSAGE FORMS, COMPOSITION AND PACKAGING
......................................................................
20
PART II: SCIENTIFIC INFORMATION
..............................................................................................
                                
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