SANDOZ CEFTRIAXONE POWDER FOR SOLUTION

Country: Kanada

Bahasa: Inggeris

Sumber: Health Canada

Bahan aktif:

CEFTRIAXONE (CEFTRIAXONE SODIUM)

Boleh didapati daripada:

SANDOZ CANADA INCORPORATED

Kod ATC:

J01DD04

INN (Nama Antarabangsa):

CEFTRIAXONE

Dos:

2G

Borang farmaseutikal:

POWDER FOR SOLUTION

Komposisi:

CEFTRIAXONE (CEFTRIAXONE SODIUM) 2G

Laluan pentadbiran:

INTRAMUSCULAR

Unit dalam pakej:

100

Jenis preskripsi:

Prescription

Kawasan terapeutik:

THIRD GENERATION CEPHALOSPORINS

Ringkasan produk:

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

Status kebenaran:

CANCELLED PRE MARKET

Tarikh kebenaran:

2018-08-01

Ciri produk

_ _
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
.......................................................................................