PIPERACILLIN AND TAZOBACTAM FOR INJECTION POWDER FOR SOLUTION

Country: Kanada

Lingwa: Ingliż

Sors: Health Canada

Ixtrih issa

Ingredjent attiv:

PIPERACILLIN (PIPERACILLIN SODIUM); TAZOBACTAM (TAZOBACTAM SODIUM)

Disponibbli minn:

SANDOZ CANADA INCORPORATED

Kodiċi ATC:

J01CR05

INN (Isem Internazzjonali):

PIPERACILLIN AND BETA-LACTAMASE INHIBITOR

Dożaġġ:

3G; 0.375G

Għamla farmaċewtika:

POWDER FOR SOLUTION

Kompożizzjoni:

PIPERACILLIN (PIPERACILLIN SODIUM) 3G; TAZOBACTAM (TAZOBACTAM SODIUM) 0.375G

Rotta amministrattiva:

INTRAVENOUS

Unitajiet fil-pakkett:

10X3.375G

Tip ta 'preskrizzjoni:

Prescription

Żona terapewtika:

EXTENDED-SPECTRUM PENICILLINS

Sommarju tal-prodott:

Active ingredient group (AIG) number: 0225919005; AHFS:

L-istatus ta 'awtorizzazzjoni:

APPROVED

Data ta 'l-awtorizzazzjoni:

2021-10-22

Karatteristiċi tal-prodott

                                _Piperacillin and Tazobactam for Injection _
_Page 1 of 47 _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
Pr
PIPERACILLIN AND TAZOBACTAM FOR INJECTION
piperacillin
sodium/tazobactam sodium
Lyophilized
Powder for Injection
For Intravenous Use Only
2 g / 0.25 g, 3 g / 0.375 g, 4 g / 0.5 g, 12 g / 1.5 g, 36 g / 4.5 g
per vial (as piperacillin sodium and as
tazobactam sodium)
Manufacturer’s Standard
Antibiotic
/ ß-lactamase Inhibitor
Sandoz Canada Inc.
110 Rue de Lauzon
Date of Revision:
October 18, 2021
Boucherville,
QC, Canada
J4B 1E6
Submission
Control No: 248976
_Piperacillin and Tazobactam for Injection _
_Page 2 of 47 _
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL
INFORMATION............................................................3
SUMMARY PRODUCT INFORMATION
.................................................................................3
INDICATIONS AND CLINICAL
USE.......................................................................................3
CONTRAINDICATIONS
...........................................................................................................5
WARNINGS AND PRECAUTIONS
..........................................................................................5
ADVERSE REACTIONS
...........................................................................................................9
DRUG
INTERACTIONS..........................................................................................................
12
DOSAGE AND
ADMINISTRATION.......................................................................................
14
OVERDOSAGE
.......................................................................................................................
19
ACTION AND CLINICAL PHARMACOLOGY
......................................................................
20
STORAGE AND
STABILITY..................................................................................................
22
SPECIAL HANDLING INSTRUCTIONS
..............................................
                                
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Dokumenti f'lingwi oħra

Karatteristiċi tal-prodott Karatteristiċi tal-prodott Franċiż 18-10-2021