LINEZOLID INJECTION SOLUTION

Riik: Kanada

keel: inglise

Allikas: Health Canada

Osta kohe

Laadi alla Toote omadused (SPC)
16-05-2018

Toimeaine:

LINEZOLID

Saadav alates:

SANDOZ CANADA INCORPORATED

ATC kood:

J01XX08

INN (Rahvusvaheline Nimetus):

LINEZOLID

Annus:

2MG

Ravimvorm:

SOLUTION

Koostis:

LINEZOLID 2MG

Manustamisviis:

INTRAVENOUS

Ühikuid pakis:

100

Retsepti tüüp:

Prescription

Terapeutiline ala:

OXAZOLIDINONES

Toote kokkuvõte:

Active ingredient group (AIG) number: 0143501003; AHFS:

Volitamisolek:

CANCELLED PRE MARKET

Loa andmise kuupäev:

2019-08-01

Toote omadused

                                _ _
_Linezolid Injection _
_Page 1 of 41_
PRODUCT MONOGRAPH
PR LINEZOLID INJECTION
Linezolid Injection
2 mg/mL, 300 mL bag
Antibacterial Agent
Sandoz Canada Inc.
145 Jules-Léger
Boucherville, QC, Canada
J4B 7K8
Date of Preparation:
May 16, 2018
Submission Control No: 215585
_ _
_Linezolid Injection _
_Page 2 of 41_
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
........................................................ 3
SUMMARY PRODUCT INFORMATION
........................................................................
3
INDICATIONS AND CLINICAL USE
.............................................................................
3
CONTRAINDICATIONS
...................................................................................................
4
WARNINGS AND PRECAUTIONS
.................................................................................
5
ADVERSE REACTIONS
...................................................................................................
9
DRUG INTERACTIONS
.................................................................................................
15
DOSAGE AND ADMINISTRATION
.............................................................................
16
OVERDOSAGE
................................................................................................................
18
ACTION AND CLINICAL PHARMACOLOGY
............................................................ 18
STORAGE AND STABILITY
.........................................................................................
23
DOSAGE FORMS, COMPOSITION AND PACKAGING
............................................. 23
PART II: SCIENTIFIC INFORMATION
..............................................................................
24
PHARMACEUTICAL INFORMATION
.........................................................................
24
CLINICAL TRIALS
.........................................................................................................
25
DETAILED PHARMACOLOGY
.................................
                                
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