DORIBAX POWDER FOR SOLUTION

Nazione: Canada

Lingua: inglese

Fonte: Health Canada

Principio attivo:

DORIPENEM (DORIPENEM MONOHYDRATE)

Commercializzato da:

JANSSEN INC

Codice ATC:

J01DH04

INN (Nome Internazionale):

DORIPENEM

Dosaggio:

500MG

Forma farmaceutica:

POWDER FOR SOLUTION

Composizione:

DORIPENEM (DORIPENEM MONOHYDRATE) 500MG

Via di somministrazione:

INTRAVENOUS

Confezione:

500ML

Tipo di ricetta:

Prescription

Area terapeutica:

CARBAPENEMS

Dettagli prodotto:

Active ingredient group (AIG) number: 0152649001; AHFS:

Stato dell'autorizzazione:

CANCELLED POST MARKET

Data dell'autorizzazione:

2013-07-03

Scheda tecnica

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PRODUCT MONOGRAPH
PR
DORIBAX
®
Doripenem for Injection
500 mg/vial doripenem (as doripenem monohydrate)
Antibacterial Agent
ATC code: J01DH04
Janssen Inc.
19 Green Belt Drive
Toronto, Ontario
M3C 1L9
www.janssen.ca
Date of Revision:
June 14, 2013
Submission Control No: 163140
All trademarks used under license.
© 2013 Janssen Inc.
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TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
......................................................... 3
SUMMARY PRODUCT INFORMATION
..................................................................................................................
3
INDICATIONS AND CLINICAL USE
........................................................................................................................
3
CONTRAINDICATIONS
.............................................................................................................................................
4
WARNINGS AND PRECAUTIONS
............................................................................................................................
4
ADVERSE REACTIONS
.............................................................................................................................................
8
DRUG INTERACTIONS
............................................................................................................................................
12
DOSAGE AND ADMINISTRATION
........................................................................................................................
13
OVERDOSAGE
..........................................................................................................................................................
17
ACTION AND CLINICAL PHARMACOLOGY
......................................................................................................
17
STORAGE AND STABILITY
.........................................................................................