(20MMOL/L) POTASSIUM CHLORIDE IN 0.9% SODIUM CHLORIDE INJECTION USP SOLUTION

Pays: Canada

Langue: anglais

Source: Health Canada

Ingrédients actifs:

SODIUM CHLORIDE; POTASSIUM CHLORIDE

Disponible depuis:

BAXTER CORPORATION

Code ATC:

B05BB01

DCI (Dénomination commune internationale):

ELECTROLYTES

Dosage:

900MG; 150MG

forme pharmaceutique:

SOLUTION

Composition:

SODIUM CHLORIDE 900MG; POTASSIUM CHLORIDE 150MG

Mode d'administration:

INTRAVENOUS

Unités en paquet:

1000ML

Type d'ordonnance:

Ethical

Domaine thérapeutique:

REPLACEMENT PREPARATIONS

Descriptif du produit:

Active ingredient group (AIG) number: 0213340001; AHFS:

Statut de autorisation:

APPROVED

Date de l'autorisation:

2012-12-07

Résumé des caractéristiques du produit

Potassium Chloride in 0.9% Sodium Chloride Injection, USP Prescribing
Information
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_Page 1 of 15_
PRESCRIBING INFORMATION
POTASSIUM CHLORIDE IN 0.9% SODIUM CHLORIDE INJECTION, USP
IN PLASTIC CONTAINER
VIAFLEX
Container
20mmol/L Potassium Chloride in Sodium in 0.9% Chloride Injection
40mmol/L Potassium Chloride in Sodium in 0.9% Chloride Injection
SOLUTION FOR INFUSION
Solutions Affecting the Electrolyte Balance
BAXTER CORPORATION
Mississauga, ON L5N 0C2
Date of Revision:
December 10, 2018
Control No. 221539
Potassium Chloride in 0.9% Sodium Chloride Injection, USP Prescribing
Information
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_Page 2 of 15_
TABLE OF CONTENTS
SUMMARY PRODUCT INFORMATION
........................................................................3
INDICATIONS AND CLINICAL USE
..............................................................................3
CONTRAINDICATIONS
...................................................................................................3
WARNINGS AND PRECAUTIONS
..................................................................................3
ADVERSE REACTIONS
....................................................................................................8
DRUG INTERACTIONS
....................................................................................................9
DOSAGE AND ADMINISTRATION
..............................................................................10
INSTRUCTIONS FOR USE AND HANDLING AND DISPOSAL
................................11
DIRECTIONS FOR USE OF VIAFLEX PLUS PLASTIC CONTAINER
......................11
OVERDOSE
......................................................................................................................12
ACTION AND CLINICAL PHARMACOLOGY
............................................................13
STORAGE AND STABILITY
..........................................................................................13
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................13
Potassium Chloride in 0.9% Sodium Chlo