SANDOZ FINGOLIMOD CAPSULE

Држава: Канада

Језик: Енглески

Извор: Health Canada

Активни састојак:

FINGOLIMOD (FINGOLIMOD HYDROCHLORIDE)

Доступно од:

SANDOZ CANADA INCORPORATED

АТЦ код:

L04AE01

INN (Међународно име):

FINGOLIMOD

Дозирање:

0.5MG

Фармацеутски облик:

CAPSULE

Састав:

FINGOLIMOD (FINGOLIMOD HYDROCHLORIDE) 0.5MG

Пут администрације:

ORAL

Јединице у пакету:

28

Тип рецептора:

Prescription

Терапеутска област:

Immunomodulatory Agents

Резиме производа:

Active ingredient group (AIG) number: 0152886001; AHFS:

Статус ауторизације:

APPROVED

Датум одобрења:

2019-03-11

Карактеристике производа

_Sandoz Fingolimod _
_Page 1 of 68 _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
SANDOZ
® FINGOLIMOD
Fingolimod capsules
Capsule, 0.5 mg fingolimod (as fingolimod hydrochloride), Oral
Sphingosine 1-phosphate receptor modulator
Sandoz Canada Inc.
110, Rue de Lauzon
Boucherville, Québec, Canada
J4B 1E6
Date of Inital Authorization:
October 31, 2019
Date of Revision:
February 23, 2022
Submission Control No: 256559
_Sandoz Fingolimod _
_Page 2 of 68 _
RECENT MAJOR LABEL CHANGES
2 Contraindications
02/2022
4 Dosage and administration
02/2022
7 Warnings and Precautions
02/2022
TABLE OF CONTENTS
RECENT MAJOR LABEL
CHANGES..............................................................................................2
TABLE OF CONTENTS
................................................................................................................2
PART I: HEALTH PROFESSIONAL INFORMATION
.......................................................................4
1
INDICATIONS
................................................................................................................4
1.1
PEDIATRICS
............................................................................................................4
1.2
GERIATRICS
............................................................................................................4
2
CONTRAINDICATIONS ..................................................................................................
4
4
DOSAGE AND ADMINISTRATION
..................................................................................
5
4.1
DOSING
CONSIDERATIONS.........................................................................................5
4.2
RECOMMENDED DOSE AND DOSAGE ADJUSTMENT
.....................................................7
4.4
ADMINISTRATION
....................................................................................................8
4.5
MISSED
DOSE.......................................................................................................