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

País: Canadá

Idioma: inglés

Fuente: Health Canada

Ingredientes activos:

SODIUM CHLORIDE; POTASSIUM CHLORIDE

Disponible desde:

BAXTER CORPORATION

Código ATC:

B05BB01

Designación común internacional (DCI):

ELECTROLYTES

Dosis:

900MG; 150MG

formulario farmacéutico:

SOLUTION

Composición:

SODIUM CHLORIDE 900MG; POTASSIUM CHLORIDE 150MG

Vía de administración:

INTRAVENOUS

Unidades en paquete:

1000ML

tipo de receta:

Ethical

Área terapéutica:

REPLACEMENT PREPARATIONS

Resumen del producto:

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

Estado de Autorización:

APPROVED

Fecha de autorización:

2012-12-07

Ficha técnica

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
_ _
_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