FSME-IMMUN SUSPENSION

Država: Kanada

Jezik: angleščina

Source: Health Canada

Kupite ga zdaj

Lastnosti izdelka Lastnosti izdelka (SPC)
10-04-2012

Aktivna sestavina:

TICK-BORNE ENCEPHALITIS VACCINE (INACTIVATED)

Dostopno od:

BAXTER CORPORATION

Koda artikla:

J07BA01

INN (mednarodno ime):

ENCEPHALITIS, TICK BORNE, INACTIVATED, WHOLE VIRUS

Odmerek:

2.4MCG

Farmacevtska oblika:

SUSPENSION

Sestava:

TICK-BORNE ENCEPHALITIS VACCINE (INACTIVATED) 2.4MCG

Pot uporabe:

INTRAMUSCULAR

Enote v paketu:

0.5ML

Tip zastaranja:

Schedule D

Terapevtsko območje:

VACCINES

Povzetek izdelek:

Active ingredient group (AIG) number: 0150541001; AHFS:

Status dovoljenje:

CANCELLED POST MARKET

Datum dovoljenje:

2014-03-03

Lastnosti izdelka

                                _ _
_Appendix I - Product Monograph Template - Schedule D _
_Page 1 of 28_
PRODUCT MONOGRAPH
FSME-IMMUN
1
Tick-Borne Encephalitis Virus Vaccine, Inactivated, with Adjuvant
2.4 µg (target value)/0.5 mL
Sterile Suspension for Intramuscular Injection
Vaccine for the Prevention of Tick-Borne Encephalitis
Manufactured by:
BAXTER AG
A-1220 Vienna, Austria
Imported and Distributed by:
Date of Revisions:
BAXTER CORPORATION
April 13, 2011
Mississauga, Ontario
CANADA
SUBMISSION CONTROL NO: 145702
APPROVAL DATE: MAY 19, 2011
This Product Monograph is the exclusive property of Baxter
Corporation. It may not be copied in
whole or in part without the express permission of Baxter Corporation.
1
FSME-IMMUN is a trademark of Baxter AG, Vienna, Austria.
_ _
_Appendix I - Product Monograph Template - Schedule D _
_Page 2 of 28_
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL
INFORMATION........................................................ 3
SUMMARY PRODUCT INFORMATION
.......................................................................
3
DESCRIPTION...................................................................................................................
3
INDICATIONS AND CLINICAL
USE.............................................................................
3
CONTRAINDICATIONS
..................................................................................................
4
WARNINGS AND
PRECAUTIONS.................................................................................
4
ADVERSE
REACTIONS...................................................................................................
6
DRUG INTERACTIONS
...................................................................................................
8
DOSAGE AND
ADMINISTRATION...............................................................................
9
ACTION AND CLINICAL PHARMACOLOGY
........................................................... 11
STORAGE AND
STABILITY.................................................................................
                                
                                Preberite celoten dokument
                                
                            

Dokumenti v drugih jezikih

Lastnosti izdelka Lastnosti izdelka francoščina 10-04-2012