IMIPENEM AND CILASTATIN FOR INJECTION USP POWDER FOR SOLUTION

País: Canadá

Idioma: inglés

Fuente: Health Canada

Ingredientes activos:

IMIPENEM; CILASTATIN (CILASTATIN SODIUM)

Disponible desde:

SANDOZ CANADA INCORPORATED

Código ATC:

J01DH51

Designación común internacional (DCI):

IMIPENEM AND CILASTATIN

Dosis:

500MG; 500MG

formulario farmacéutico:

POWDER FOR SOLUTION

Composición:

IMIPENEM 500MG; CILASTATIN (CILASTATIN SODIUM) 500MG

Vía de administración:

INTRAVENOUS

Unidades en paquete:

10

tipo de receta:

Prescription

Área terapéutica:

CARBAPENEMS

Resumen del producto:

Active ingredient group (AIG) number: 0218820001; AHFS:

Estado de Autorización:

APPROVED

Fecha de autorización:

2010-10-20

Ficha técnica

_Imipenem and Cilastatin for Injection USP _
_Page 1 of 55_
_ _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
IMIPENEM AND CILASTATIN FOR INJECTION USP
500 mg imipenem and 500 mg cilastatin (as cilastatin sodium) per vial
Sterile powder for solution, I.V. Infusion
Antibiotic
Sandoz Canada Inc.
110 Rue de Lauzon
Boucherville, (Québec), Canada
J4B 1E6
Date of Initial Authorization:
December 21, 2010
Date of Revision:
July 26, 2022
Submission Control Number: 260930
_Imipenem and Cilastatin for Injection USP _
_Page 2 of 55_
RECENT MAJOR LABEL CHANGES
4 DOSAGE AND ADMINISTRATION, 4.1 Dosing Considerations
07/2022
4 DOSAGE AND ADMINISTRATION
07/2022
7 WARNINGS AND PRECAUTIONS
07/2022
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
...............................................................................................................
5
1.2 GERIATRICS
...............................................................................................................
5
2
CONTRAINDICATIONS......................................................................................................
6
3
SERIOUS WARNINGS AND PRECAUTIONS BOX
................................................................. 6
4
DOSAGE AND ADMINISTRATION
.....................................................................................
6
4.1 DOSING
CONSIDERATIONS............................................................................................
6
4.2 RECO