CEFAZOLIN SODIUM FOR INJECTION BP POWDER FOR SOLUTION

Nazione: Canada

Lingua: inglese

Fonte: Health Canada

Compra

Scheda tecnica Scheda tecnica (SPC)
14-09-2022

Principio attivo:

CEFAZOLIN (CEFAZOLIN SODIUM)

Commercializzato da:

STERIMAX INC

Codice ATC:

J01DB04

INN (Nome Internazionale):

CEFAZOLIN

Dosaggio:

2G

Forma farmaceutica:

POWDER FOR SOLUTION

Composizione:

CEFAZOLIN (CEFAZOLIN SODIUM) 2G

Via di somministrazione:

INTRAMUSCULAR

Confezione:

15G/50G

Tipo di ricetta:

Prescription

Dettagli prodotto:

Active ingredient group (AIG) number: 0109442010; AHFS:

Stato dell'autorizzazione:

APPROVED

Data dell'autorizzazione:

2022-02-11

Scheda tecnica

                                PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
CEFAZOLIN SODIUM FOR INJECTION BP
Powder for Solution, 1 gram, 2 grams and 10 grams Cefazolin (as
cefazolin sodium) per vial
Intravenous, Intramuscular
BP
Antibiotic
SteriMax Inc.
Date of Initial Authorization: JUN 24, 2020
2770 Portland Drive
Oakville, ON
Date of Revision: SEP 14, 2022
L6H 6R4
Control No: 263261
Pr
CEFAZOLIN SODIUM FOR INJECTION BP Page 2 of 21
RECENT MAJOR LABEL CHANGES
7 WARNINGS AND PRECAUTIONS, SKIN
01/2021
7 WARNINGS AND PRECAUTIONS, RENAL
09/2022
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
4.2
Recommended Dose and Dosage Adjustment
.................................................................... 5
4.3
Reconstitution
......................................................................................................................
7
4.4
Administration
.................................................................................
                                
                                Leggi il documento completo
                                
                            

Documenti in altre lingue

Scheda tecnica Scheda tecnica francese 14-09-2022

Cerca alert relativi a questo prodotto