TAZOCIN POWDER FOR SOLUTION

País: Canadà

Idioma: anglès

Font: Health Canada

ingredients actius:

PIPERACILLIN (PIPERACILLIN SODIUM); TAZOBACTAM (TAZOBACTAM SODIUM)

Disponible des:

PFIZER CANADA ULC

Codi ATC:

J01CR05

Designació comuna internacional (DCI):

PIPERACILLIN AND BETA-LACTAMASE INHIBITOR

Dosis:

4G; 500MG

formulario farmacéutico:

POWDER FOR SOLUTION

Composición:

PIPERACILLIN (PIPERACILLIN SODIUM) 4G; TAZOBACTAM (TAZOBACTAM SODIUM) 500MG

Vía de administración:

INTRAVENOUS

Unidades en paquete:

23.15ML

tipo de receta:

Prescription

Área terapéutica:

EXTENDED-SPECTRUM PENICILLINS

Resumen del producto:

Active ingredient group (AIG) number: 0225919002; AHFS:

Estat d'Autorització:

CANCELLED POST MARKET

Data d'autorització:

2015-04-27

Fitxa tècnica

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_TAZOCIN (Piperacillin Sodium/Tazobactam Sodium)_
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PRODUCT MONOGRAPH
PR
TAZOCIN
®
Piperacillin and Tazobactam powder for injection
2.0g/0.25g, 3g/0.375g, 4.0g/0.5g per vial (as piperacillin sodium and
tazobactam sodium)
Lyophilized Powder for Injection
Antibiotic/ß-lactamase Inhibitor
Pfizer Canada Inc
17,300 Trans-Canada Highway
Kirkland, Quebec H9J 2M5
Date of Revision:
April 8, 2014
Submission Control No: 171562
®
TM Wyeth Holdings Corporation, Pfizer Canada Inc., Licensee
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_TAZOCIN (Piperacillin Sodium/Tazobactam Sodium)_
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_Page 2 of 43 _
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
..........................................................................................23
SPECIAL HANDLING INSTRUCTIONS
.......................................................................23
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................23
PART II: SCIENTIFIC INFORMATION
....