MDV-1 LIVING VACCINE

Country: Awstralja

Lingwa: Ingliż

Sors: APVMA (Australian Pesticides and Veterinary Medicines Authority)

Ixtrih issa

Ingredjent attiv:

MAREK'S DISEASE

Disponibbli minn:

INTERVET AUSTRALIA PTY LIMITED

INN (Isem Internazzjonali):

MDV (BH 16)

Għamla farmaċewtika:

MISC. VACCINES OR ANTI SERA

Kompożizzjoni:

MAREK'S DISEASE VACCINE-GENERAL Active 0.0 U

Unitajiet fil-pakkett:

!1mL Amp; !500 Doses; *1.8mL Amp; *1000Doses; 200mL; Diluent

Klassi:

VM - Veterinary Medicine

Manifatturat minn:

INTERVET AUSTRALIA

Grupp terapewtiku:

POULTRY CHICKS | CHICKENS | DAY OLD CHICKS | HATCHLINGS

Żona terapewtika:

IMMUNOTHERAPY

Indikazzjonijiet terapewtiċi:

MAREK'S DISEASE | HERPES VIRUS OF TURKEYS (HVT)

Sommarju tal-prodott:

Poison schedule: 0; Withholding period: WHP: Nil.; Host/pest details: POULTRY CHICKS: [MAREK'S DISEASE]; Poison schedule: 0; Withholding period: ; Host/pest details: POULTRY CHICKS: [MAREK'S DISEASE]; For the active immunisation of chickens at 1 day old against Marek's Disease when used in association with but not mixed with Intervet's HVT-CA vaccine.

L-istatus ta 'awtorizzazzjoni:

Registered

Data ta 'l-awtorizzazzjoni:

2023-07-01

Fuljett ta 'informazzjoni

                                Intervel Australia Pty Llmtted-
Label
For
MDV
~
1 Living Vaccine
AB.N.
79 008 467 034
Vaccine
Ampoule
Label
V5>V6
Version 6
}:>
Appropriate doses
incorporated
for
ampoule
size.
)-
Either 1 mL (500 dose) OR 1.8 mL (1000 dose) to be deleted as
appropriate for
batch.
'FORAMliAiiREAiMEifr
ONLY
MDV.1
LiYlng
Yal:e!ne
1/111.(500
d_ll
U
IJ'i
(1000
dole)
READ
THE
ENa.oaEO
LEAFLET
BEfORE
USING
TIIS
PRODUCT
S"'-In~idnilrogOl'l
[IlJ
Exp:
lnIer¥oIAuohkP.t. Ph:
(GJ)
5442$(111
Milk
52319/
0'00;(
_231712002_
Signatur
MDV~1
Label suite
,
.
Page I
of3
Intervet
Austro.lio.
Pty Ltd
MDV-l
Living
Vaccine
-
Product
Leo.flet
Version
8
READ SAFETY DIRECTIONS BEFORE
OPENING OR USING
FOR
ANIMAL
TREATMENT ONLY
MDV·1
Living
Vaccine
Active constituent: Marek's diseasevirus,
living,
cell-
associated, strain BH 16.
Minimum
titre at end of
shelf life:
106.09
TCID
so
per
mL
For the active immunisatlon of chickens at 1 day-old
against Marek's
Disease
when used in association
with but not mixed with Intervet's
HVT-CA
Vaccine.
1
mL
(500
dose)/1.8 mL
(1000
dose) per ampoule
(delete
as
appropriate)
DIRECTIONS FOR USE
Restraints:
•
Give subcutaneously only.
Precautions:
•
MDV-1
living
Vaccine Is not recommended
for mixing
with
Intervet's
HVT-CA VaccIne
in
a single Injection.
•
Vaccinate only healthy birds.
•
Avoid placing chickens In contaminated
facilities.
•
Avoid stress conditions during and following
vaccination.
•
Ensure exposure to disease Is minimised as
much
as
possible
Dosage and
Administration:
•
USE ALL PRODUCTWITHIN
1
HOUR
OF
OPENING
&
MIXING
•
Administer a full dose to each bird.
•
Vaccinate all birds on the farm at one time.
•
The vaccine is recommended tor use in
one-day-old chicks.
•
Sterilise all injection apparatusby
boiting
(or
equivalent)before use. Avoid use of
strong
disinfectants on apparatus usedfor live
vaccines.
•
A single dose of the
vaccine
is administered
subcutaneously. Two 500 dose ampoulesor one
1000 dose ampouleof vaccine and one 200 mL
pack of
IntervetMareks Disease
Vaccines
Diluent
are requir
                                
                                Aqra d-dokument sħiħ
                                
                            

Karatteristiċi tal-prodott

                                PRODUCT NAME: MDV-1 LIVING VACCINE
MATERIAL SAFETY DATA SHEET
THIS REVISION ISSUED: JULY, 2009
PAGE: 1 OF 6
MATERIAL SAFETY DATA SHEET
Issued by: Intervet Australia Pty Limited Phone: 1 800 033 461
(Business Hours)
Poisons Information Centre: 13 11 26 from anywhere in Australia, (0800
764 766 in New Zealand)
SUBSTANCE:
Cells SPF chicken embryo, containing Marek’s Disease Virus, serotype
1 (living,
attenuated) freeze dried. Supplied with an aqueous solution of
stabilisers and buffering
agents.
TRADE NAME:
MDV-1 LIVING VACCINE
PRODUCT CODE:
3958
RECOMMENDED USE:
For the active immunisation of chickens at 1 day old against Marek's
Disease when used
in association with but not mixed with Intervet's HVT-CA vaccine.
APVMA NO:
52379
CREATION DATE:
February, 2007
THIS VERSION ISSUED:
July, 2009
and is valid for 5 years from this date.
STATEMENT OF HAZARDOUS NATURE:
THIS PRODUCT IS CLASSIFIED AS:
Not classified as hazardous according to the criteria of SWA.
Not a Dangerous Good according to the Australian Dangerous Goods (ADG)
Code.
RISK PHRASES:
Not Hazardous - No criteria found.
SAFETY PHRASES:
S23, S37, S24/25. Do not breathe mists. Wear suitable gloves. Avoid
contact with skin and eyes.
SUSDP CLASSIFICATION:
None allocated.
ADG CLASSIFICATION:
None allocated. Not a Dangerous Good under the ADG Code.
UN NUMBER:
None allocated
PHYSICAL DESCRIPTION & COLOUR:
Two component system; attenuated virus is a pellet or powder while
diluent is a
clear, colourless liquid.
ODOUR:
Mild odour.
MAJOR HEALTH HAZARDS:
no significant risk factors have been found for this product.
INHALATION:
SHORT TERM EXPOSURE:
Available data indicates that this product is not harmful. However
product may be mildly
irritating, although unlikely to cause anything more than mild
transient discomfort.
LONG TERM EXPOSURE:
No data for health effects associated with long term inhalation.
SKIN CONTACT:
SHORT TERM EXPOSURE:
Available data indicates that this product is not harmful. It should
present no hazards in
normal use. However product may be mildly irri
                                
                                Aqra d-dokument sħiħ