SANDOZ CEFTRIAXONE POWDER FOR SOLUTION

Nazione: Canada

Lingua: inglese

Fonte: Health Canada

Principio attivo:

CEFTRIAXONE (CEFTRIAXONE SODIUM)

Commercializzato da:

SANDOZ CANADA INCORPORATED

Codice ATC:

J01DD04

INN (Nome Internazionale):

CEFTRIAXONE

Dosaggio:

2G

Forma farmaceutica:

POWDER FOR SOLUTION

Composizione:

CEFTRIAXONE (CEFTRIAXONE SODIUM) 2G

Via di somministrazione:

INTRAMUSCULAR

Confezione:

100

Tipo di ricetta:

Prescription

Area terapeutica:

THIRD GENERATION CEPHALOSPORINS

Dettagli prodotto:

Active ingredient group (AIG) number: 0117292002; AHFS:

Stato dell'autorizzazione:

CANCELLED PRE MARKET

Data dell'autorizzazione:

2018-08-01

Scheda tecnica

_ _
PRODUCT MONOGRAPH
SANDOZ CEFTRIAXONE
Sterile Ceftriaxone for Injection BP
1 G AND 2 G CEFTRIAXONE PER VIAL (INCORPORATED AS CEFTRIAXONE SODIUM)
ANTIBIOTIC
Sandoz Canada Inc.
Date of Revision: January 15, 2010
145 Jules-Léger
Boucherville, QC, Canada
J4B 7K8
CONTROL # : 133307
_Sandoz Ceftriaxone _
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TABLE OF CONTENTS
HEALTH PROFESSIONAL
INFORMATION.........................................................................
3
ACTION
.....................................................................................................................................
3
INDICATIONS AND CLINICAL
USES...................................................................................
3
CONTRAINDICATIONS
..........................................................................................................
4
WARNINGS...............................................................................................................................
4
PRECAUTIONS.........................................................................................................................
6
ADVERSE
REACTIONS...........................................................................................................
8
SYMPTOMS AND TREATMENT OF OVERDOSAGE
....................................................... 10
DOSAGE AND
ADMINISTRATION.....................................................................................
10
ADMINISTRATION................................................................................................................
11
PHARMACEUTICAL
INFORMATION.................................................................................
13
DRUG
SUBSTANCE...............................................................................................................
13
DRUG
PRODUCT....................................................................................................................
13
RECONSTITUTION
.......................................................................................