CEFTAZIDIME FOR INJECTION BP POWDER FOR SOLUTION

Země: Kanada

Jazyk: angličtina

Zdroj: Health Canada

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Aktivní složka:

CEFTAZIDIME (CEFTAZIDIME PENTAHYDRATE)

Dostupné s:

STERIMAX INC

ATC kód:

J01DD02

INN (Mezinárodní Name):

CEFTAZIDIME

Dávkování:

6G

Léková forma:

POWDER FOR SOLUTION

Složení:

CEFTAZIDIME (CEFTAZIDIME PENTAHYDRATE) 6G

Podání:

INTRAVENOUS

Jednotky v balení:

30ML

Druh předpisu:

Prescription

Terapeutické oblasti:

THIRD GENERATION CEPHALOSPORINS

Přehled produktů:

Active ingredient group (AIG) number: 0116900009; AHFS:

Stav Autorizace:

APPROVED

Datum autorizace:

2015-02-27

Charakteristika produktu

                                PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
CEFTAZIDIME FOR INJECTION BP
Powder for Solution,1 g, 2 g, 3 g and 6 g of ceftazidime (as
ceftazidime pentahydrate) per vial
Intravenous, Intramuscular
BP
Antibiotic
STERIMAX INC.
2770 Portland Drive
Oakville, ON L6H 6R4
Date of Initial Authorization:
February 23, 2015
Date of Revision:
May 2, 2023
Control No.: 269730
Ceftazidime for Injection BP
Page 2 of 60
_ _
RECENT MAJOR LABEL CHANGES
SECTIONS
DATE
3 SERIOUS WARNINGS AND PRECAUTIONS BOX
05/2023
4 DOSAGE AND ADMINISTRATION, 4.1 Dosing Consideration, 4.2
Recommended Dose and Dosage Adjustment, 4.3 Reconstitution, 4.4
Administration
05/2023
7 WARNINGS AND PRECAUTIONS, Clostridium difficile-Associated
Disease, Immune, Neurologic, Renal, Skin
05/2023
8 ADVERSE REACTIONS, 8.2 Clinical Trial Adverse Reactions
05/2023
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
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2
PART I: HEALTH PROFESSIONAL INFORMATION
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4
1
INDICATIONS
..................................................................................................................
4
1.1
Pediatrics
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5
1.2
Geriatrics
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5
2
CONTRAINDICATIONS
.....................................................................................................
5
3
SERIOUS WARNINGS AND PRECAUTIONS BOX
................................................................ 6
4
DOSAGE AND ADMINISTRATION
...............................................................................
                                
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