EQUIVAC T VACCINE

Country: Аустралија

Језик: Енглески

Извор: APVMA (Australian Pesticides and Veterinary Medicines Authority)

Активни састојак:

CLOSTRIDIUM TETANI UF TOXOID; THIOMERSAL

Доступно од:

ZOETIS AUSTRALIA PTY LTD

INN (Међународно име):

Cl tetani - toxoid

Фармацеутски облик:

MISC. VACCINES OR ANTI SERA

Састав:

CLOSTRIDIUM TETANI UF TOXOID VACCINE-TOXOID Active 0.0 P; THIOMERSAL MERCURY Other 0.1 mg/ml

Јединице у пакету:

10mL Vial; 1mL Syr

Класа:

VM - Veterinary Medicine

Произведен од:

ZOETIS AUSTRALIA

Терапеутска група:

CATTLE | DOG | GOAT | HORSE | PIGS | SHEEP | BEEF | BILLY | BITCH | BOAR | BOS INDICUS | BOS TAURUS | BOVINE | BUCK | BUFFALO |

Терапеутска област:

IMMUNOTHERAPY

Терапеутске индикације:

TETANUS | TETANUS VACCINATION

Резиме производа:

Poison schedule: 0; Withholding period: WHP: Meat:Nil Milk:Nil; Host/pest details: CATTLE: [TETANUS]; DOG: [TETANUS]; GOAT: [TETANUS]; HORSE: [TETANUS]; PIGS: [TETANUS]; SHEEP: [TETANUS]; Poison schedule: 0; Withholding period: ; Host/pest details: CATTLE: [TETANUS]; DOG: [TETANUS]; GOAT: [TETANUS]; HORSE: [TETANUS]; PIGS: [TETANUS]; SHEEP: [TETANUS]; For the immunisation of horses, dogs, cattle, sheep, goats and pigs against tetanus.

Статус ауторизације:

Registered

Датум одобрења:

2023-07-01

Информативни летак

AUSTRALIAN GOVERNMENT
Australian Pesticides and
Veterinary Medicines Authority
APPENDIX 2
TEMPLATE FOR RELEVANT LABEL PARTICULARS (RLPS)
(VETERINARY PRODUCTS)
Select appropriate:
13
New Product (include all applicable RLPs) OR
Er Variation (highlight instructions that are being varied). Approval
no. of label being varied: 51772/0306.
Signal heading:
FOR ANIMAL TREATMENT ONLY
Product name:
Equivac® T Vaccine
Active constituent/s:
Equivac T is a purified adjuvanted vaccine containing the formalinised
toxin of
Clostridium
tetani
(20
Lf/mL) The adjuvant, which is an aluminium salt, increases the level
and
duration of the immunity afforded by the vaccine. The type of adjuvant
and the purification
procedures used ensure maximum protection of animals with minimum risk
of local
reactions at the site of injection. Thiomersal 0.1 mg/mL is added as a
preservative.
Statement of claims:
For the immunisation of horses, dogs, cattle, sheep, goats and pigs
against tetanus.
Net contents:
1mL dose syringe.
10mL dose vial.
Directions
for Use
Heading:
"AK\
4,10.
RLP
Approved
DIRECTIONS FOR USE
READ THE ENCLOSED LEAFLET BEFORE USING THIS PRODUCT
Contents must be left in outer package until immediately before use
Shake well before use and keep thoroughly mixed during use
Use all product within 12 hours of opening.
It is important that the vaccine is kept properly mixed before and
during use. There may
be settling of the adjuvant after storage but material is easily
resuspended by inversion of
the syringe or vial.
Before vaccine is injected, the proposed site of inoculation on the
animal's skin may be
cleaned by swabbing with cotton-wool soaked in a suitable antiseptic
solution, such as
methylated spirits.
Restraints:
N/A
Contraindications:
N/A
Precautions:
N/A
Side effects:
Localised swelling may develop at the site of injection and a firm
nodular lump may
persist for some weeks or even months. There may be temporary
lameness. Allergic
reactions such as anaphlylaxis occur rarely with all vaccines and may
require appropriate
treatment

Карактеристике производа

PRODUCT NAME: EQUIVAC
® T VACCINE
PAGE: 1 OF 5
THIS REVISION ISSUED:
MATERIAL SAFETY DATA SHEET
Issued by: Pfizer Australia Pty Ltd
Phone: [phone]
SECTION 1 - IDENTIFICATION OF CHEMICAL PRODUCT AND COMPANY
Pfizer Australia Pty Ltd
38-42 Wharf Road
West Ryde NSW 2114
Tel: [phone]
Fax: [phone]
____________________________________
PFIZER AUSTRALIA PTY LTD
A.B.N. 50 008 422 348
SUBSTANCE:
Saline suspension of vaccine ingredients.
TRADE NAME:
EQUIVAC
® T VACCINE
PFIZER MSDS CODE:
0343
PRODUCT USE:
Vaccine for the prevention of tetanus in horses, dogs, cattle, sheep,
goats and pigs
CREATION DATE:
AUGUST, 2004
THIS VERSION ISSUED:
APRIL 2010
and is valid for 5 years from this date.
SECTION 2 - HAZARDS IDENTIFICATION
STATEMENT OF HAZARDOUS NATURE
This product is classified as:
Not classified as hazardous according to the criteria of SWA
Australia.
Not a Dangerous Good according to the Australian Dangerous Goods (ADG)
Code.
RISK PHRASES:
Not Hazardous - No criteria found.
SAFETY PHRASES:
Not Hazardous - No criteria found.
SUSDP CLASSIFICATION:
None allocated. (NZ S2)
ADG CLASSIFICATION:
None allocated. Not a Dangerous Good.
UN NUMBER:
None allocated
E
E
E
M
M
M
E
E
E
R
R
R
G
G
G
E
E
E
N
N
N
C
C
C
Y
Y
Y
O
O
O
V
V
V
E
E
E
R
R
R
V
V
V
I
I
I
E
E
E
W
W
W
PHYSICAL DESCRIPTION & COLOUR
: Aqueous liquid suspension.
ODOUR:
No odour.
MAJOR HEALTH HAZARDS:
no significant risk factors have been found for this product.
P
P
P
O
O
O
T
T
T
E
E
E
N
N
N
T
T
T
I
I
I
A
A
A
L
L
L
H
H
H
E
E
E
A
A
A
L
L
L
T
T
T
H
H
H
E
E
E
F
F
F
F
F
F
E
E
E
C
C
C
T
T
T
S
S
S
INHALATION
SHORT TERM EXPOSURE:
Significant inhalation exposure is considered to be unlikely.
Available data indicates that this
product is not harmful. In addition product is unlikely to cause any
discomfort or irritation.
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 mil