TRANEXAMIC ACID INJECTION SOLUTION

Pajjiż: Kanada

Lingwa: Ingliż

Sors: Health Canada

Ixtrih issa

Ingredjent attiv:

TRANEXAMIC ACID

Disponibbli minn:

JAMP PHARMA CORPORATION

Kodiċi ATC:

B02AA02

INN (Isem Internazzjonali):

TRANEXAMIC ACID

Dożaġġ:

100MG

Għamla farmaċewtika:

SOLUTION

Kompożizzjoni:

TRANEXAMIC ACID 100MG

Rotta amministrattiva:

INTRAVENOUS

Unitajiet fil-pakkett:

15G/50G

Tip ta 'preskrizzjoni:

Prescription

Żona terapewtika:

HEMOSTATICS

Sommarju tal-prodott:

Active ingredient group (AIG) number: 0114760002; AHFS:

L-istatus ta 'awtorizzazzjoni:

APPROVED

Data ta 'l-awtorizzazzjoni:

2020-03-17

Karatteristiċi tal-prodott

                                _ Tranexamic Acid Injection (tranexamic acid) _Page 1 of 24
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
TRANEXAMIC ACID INJECTION
Tranexamic acid injection
Solution, 100 mg / mL, Intravenous
House Standard
Antifibrinolytic agent
JAMP Pharma Corporation
1310 rue Nobel
Boucherville Quebec
J4B 5H3, Canada
Date of Initial Authorization:
March 16, 2020
Date of Revision:
November 28, 2022
Submission Control Number: 265633
_ Tranexamic Acid Injection (tranexamic acid) _Page 2 of 24
RECENT MAJOR LABEL CHANGES
2 CONTRAINDICATIONS
11/2022
4 DOSAGE AND ADMINISTRATION, 4.4 Administration
11/2022
7 WARNINGS AND PRECAUTIONS
11/2022
TABLE OF CONTENTS
SECTIONS OR SUBSECTIONS THAT ARE NOT APPLICABLE AT THE TIME OF
AUTHORIZATION ARE NOT LISTED.
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.......................................................................................
4
4.1
Dosing Considerations
..............................................................................................
4
4.2
Recommended Dose and Dosage Adjustment
......................................................... 5
4.3
Reconstitution
.................
                                
                                Aqra d-dokument sħiħ
                                
                            

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Karatteristiċi tal-prodott Karatteristiċi tal-prodott Franċiż 28-11-2022

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