INNOHEP SOLUTION

Pays: Canada

Langue: anglais

Source: Health Canada

Achète-le

Ingrédients actifs:

TINZAPARIN SODIUM

Disponible depuis:

LEO PHARMA INC

Code ATC:

B01AB10

DCI (Dénomination commune internationale):

TINZAPARIN

Dosage:

20000UNIT

forme pharmaceutique:

SOLUTION

Composition:

TINZAPARIN SODIUM 20000UNIT

Mode d'administration:

SUBCUTANEOUS

Unités en paquet:

0.5ML

Type d'ordonnance:

Prescription

Domaine thérapeutique:

HEPARINS

Descriptif du produit:

Active ingredient group (AIG) number: 0124929003; AHFS:

Statut de autorisation:

APPROVED

Date de l'autorisation:

2010-10-14

Résumé des caractéristiques du produit

                                _ _
_innohep® (tinzaparin sodium) Product Monograph, version 8.0 _
_Page 1 of 45_
PRODUCT MONOGRAPH
PR
INNOHEP®
tinzaparin sodium
Sterile solution for SC injection
MULTI-DOSE VIAL
10,000 anti-Xa IU/mL
20,000 anti-Xa IU/mL
PRE-FILLED SYRINGE WITH SAFETY NEEDLE DEVICE
2,500 anti-Xa IU/0.25 mL
3,500 anti-Xa IU/0.35 mL
4,500 anti-Xa IU/0.45 mL
8,000 anti-Xa IU/0.4 mL
10,000 anti-Xa IU/0.5 mL
12,000 anti-Xa IU/0.6 mL
14,000 anti-Xa IU/0.7 mL
16,000 anti-Xa IU/0.8 mL
18,000 anti-Xa IU/0.9 mL
Ph. Eur.
Anticoagulant / Antithrombotic
LEO Pharma Inc
Thornhill, ON
L3T 7W8
www.leo-pharma.com/canada
Date of Revision:
Date of Approval:
MAY 26, 2017
Submission Control No:
202366
® Registered trademark of LEO Pharma A/S used under license by LEO
Pharma Inc., Thornhill, ON
eDoc-000592317 - Version 5.0
_ _
_innohep® (tinzaparin sodium) Product Monograph, version 8.0 _
_Page 2 of 45_
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
.........................................................3
SUMMARY PRODUCT INFORMATION
........................................................................3
INDICATIONS AND CLINICAL USE
..............................................................................3
CONTRAINDICATIONS
...................................................................................................4
WARNINGS AND PRECAUTIONS
..................................................................................5
ADVERSE REACTIONS
..................................................................................................14
DRUG INTERACTIONS
..................................................................................................19
DOSAGE AND ADMINISTRATION
..............................................................................20
OVERDOSAGE
................................................................................................................26
ACTION AND CLINICAL PHARMACOLOGY
............................................................26
STORAGE AND STABILITY
.....................
                                
                                Lire le document complet
                                
                            

Documents dans d'autres langues

Rechercher des alertes liées à ce produit

Afficher l'historique des documents