CAYSTON POWDER FOR SOLUTION

Land: Canada

Språk: engelsk

Kilde: Health Canada

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Preparatomtale Preparatomtale (SPC)
15-05-2020

Aktiv ingrediens:

AZTREONAM

Tilgjengelig fra:

GILEAD SCIENCES CANADA INC

ATC-kode:

J01DF01

INN (International Name):

AZTREONAM

Dosering :

75MG

Legemiddelform:

POWDER FOR SOLUTION

Sammensetning:

AZTREONAM 75MG

Administreringsrute:

INHALATION

Enheter i pakken:

2ML

Resept typen:

Prescription

Terapeutisk område:

MONOBACTAMS

Produkt oppsummering:

Active ingredient group (AIG) number: 0122819004; AHFS:

Autorisasjon status:

APPROVED

Autorisasjon dato:

2009-09-11

Preparatomtale

                                PRODUCT MONOGRAPH
PR
CAYSTON
®
AZTREONAM FOR INHALATION SOLUTION
75 MG AZTREONAM / VIAL
ANTIBIOTIC
_(ATC J01DF01) _
_ _
_ _
_ _
_ _
_ _
Gilead Sciences, Inc.
Foster City, CA 94404
USA
Gilead Sciences Canada, Inc.
Mississauga, ON
L5N 2W3
www.gilead.ca
Control No.: 234938_ _
Date of Revision:
May 15, 2020
CAYSTON

(aztreonam for inhalation solution)
Product Monograph
2
TABLE OF CONTENTS
PART I.
HEALTH PROFESSIONAL INFORMATION
................................................................................
3
SUMMARY PRODUCT INFORMATION
..................................................................................................
3
INDICATIONS AND CLINICAL USE
........................................................................................................
3
CONTRAINDICATIONS
.............................................................................................................................
3
WARNINGS AND PRECAUTIONS
............................................................................................................
4
ADVERSE REACTIONS
..............................................................................................................................
6
DRUG INTERACTIONS
..............................................................................................................................
9
DOSAGE AND ADMINISTRATION
........................................................................................................
10
OVERDOSAGE
..........................................................................................................................................
11
ACTION AND CLINICAL PHARMACOLOGY
.......................................................................................
11
STORAGE AND STABILITY
....................................................................................................................
12
SPECIAL HANDLING
INSTRUCTIONS..................................................................................................
13
DOSAGE F
                                
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