CEFTAZIDIME FOR INJECTION, USP POWDER FOR SOLUTION

Země: Kanada

Jazyk: angličtina

Zdroj: Health Canada

Koupit nyní

Aktivní složka:

CEFTAZIDIME

Dostupné s:

FRESENIUS KABI CANADA LTD

ATC kód:

J01DD02

INN (Mezinárodní Name):

CEFTAZIDIME

Dávkování:

2G

Léková forma:

POWDER FOR SOLUTION

Složení:

CEFTAZIDIME 2G

Podání:

INTRAVENOUS

Jednotky v balení:

11.2ML

Druh předpisu:

Prescription

Terapeutické oblasti:

THIRD GENERATION CEPHALOSPORINS

Přehled produktů:

Active ingredient group (AIG) number: 0116900002; AHFS:

Stav Autorizace:

APPROVED

Datum autorizace:

2006-10-05

Charakteristika produktu

                                _ _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
CEFTAZIDIME FOR INJECTION, USP
1 g / vial, 2 g / vial, 6 g / vial
Sterile Powder for Solution
For Intramuscular or Intravenous Use
Antibiotic
ATC Code: J01DD02
FRESENIUS KABI CANADA LTD.
165 Galaxy Blvd, Suite 100
Toronto, ON M9W 0C8
Date of Initial Authorization:
MAR 24, 2015
Date of Revision:
FEB 17, 2022
Submission Control Number: 254560
_Product Monograph Master Template _
_ _
_Template Date: September 2020 _
_Ceftazidime for Injection, USP _
_ _
_Page 2 of 45 _
RECENT MAJOR LABEL CHANGES
SECTION
DATE
1 INDICATIONS
[02/2022]
4 DOSAGE AND ADMINISTRATION, 4.2 Recommended Dose and
Dosage Adjustment
[02/2022]
7 WARNINGS AND PRECAUTIONS, Carcinogenesis and Mutagenesis,
Sensitivity/Resistance, Skin and Sodium Content
[02/2022]
7 WARNINGS AND PRECAUTIONS, 7.1.1 Pregnant Women
[02/2022]
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......................................................................................................5
4
DOSAGE AND ADMINISTRATION
.......................................................................................5
4.1
Dosing Considerations
...............................................
                                
                                Přečtěte si celý dokument
                                
                            

Dokumenty v jiných jazycích

Charakteristika produktu Charakteristika produktu francouzština 17-02-2022

Vyhledávejte upozornění související s tímto produktem