INFLECTRA POWDER FOR SOLUTION

Land: Kanada

Språk: engelska

Källa: Health Canada

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Ladda ner Produktens egenskaper (SPC)
06-07-2020

Aktiva substanser:

INFLIXIMAB

Tillgänglig från:

CELLTRION HEALTHCARE CO LTD

ATC-kod:

L04AB02

INN (International namn):

INFLIXIMAB

Dos:

100MG

Läkemedelsform:

POWDER FOR SOLUTION

Sammansättning:

INFLIXIMAB 100MG

Administreringssätt:

INTRAVENOUS

Enheter i paketet:

15G/50G

Receptbelagda typ:

Prescription

Terapiområde:

DISEASE-MODIFYING ANTIRHEUMATIC AGENTS

Produktsammanfattning:

Active ingredient group (AIG) number: 0144162001; AHFS:

Bemyndigande status:

APPROVED

Tillstånd datum:

2014-06-04

Produktens egenskaper

                                _INFLECTRA_
_® _
_Product Monograph_
Page 1 of 115
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
INFLECTRA
®
(infliximab for injection)
Powder for Solution, Sterile, Lyophilized, 100 mg/vial, Intravenous
Infusion
PROFESSED STANDARD
Biological Response Modifier
Manufactured by:
Celltrion Healthcare Co., Ltd.
19, Academy-ro 51 beon-gil,
Yeonsu-gu, Incheon
Republic of Korea
22014
Imported and distributed by:
Pfizer Canada ULC
17300 Trans-Canada Highway
Kirkland, Québec
H9J 2M5
Date of Initial Approval:
January 15, 2014
Date of Revision: March 11,
2020
Submission Control No: 237374
Date of Revision: July 6, 2020
_INFLECTRA_
_® _
_Product Monograph_
Page 2 of 115
RECENT MAJOR LABEL CHANGES
NOT APPLICABLE
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
................................................................. 4
1
INDICATIONS
.................................................................................................................
4
1.1
Pediatrics
...............................................................................................................
5
1.2
Geriatrics (≥ 65_ _years of age)
.................................................................................
5
2
CONTRAINDICATIONS
..................................................................................................
6
3
SERIOUS WARNINGS AND PRECAUTIONS BOX
........................................................ 6
4
DOSAGE AND ADMINISTRATION
................................................................................
7
4.1
Recommended Dose and Dosage Adjustment
....................................................... 7
4.2
Administration
........................................................................................................
9
4.3
Reconstitution
......................................................................................................
10
4.4
Missed Dose
........................................................................................................
10
5
OVE
                                
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