ULTRAVAC BEF VACCINE

Valsts: Austrālija

Valoda: angļu

Klimata pārmaiņas: APVMA (Australian Pesticides and Veterinary Medicines Authority)

Aktīvā sastāvdaļa:

BOVINE EPHEMERAL FEVER VIRUS (BEFV)

Pieejams no:

ZOETIS AUSTRALIA PTY LTD

SNN (starptautisko nepatentēto nosaukumu):

bovine ephemeral fever virus

Zāļu forma:

PARENTERAL LIQUID/SOLUTION/SUSPENSION

Kompozīcija:

BOVINE EPHEMERAL FEVER VIRUS (BEFV) VACCINE-VIRAL Active 0.0 P

Vienības iepakojumā:

#10x20mL; #Diluent; #vials; 1 x 10 dose vaccine; 1 x 20 mL diluent; 10x10 D.V.; Dose = 2mL

Klase:

VM - Veterinary Medicine

Ražojis:

ZOETIS AUSTRALIA

Ārstniecības grupa:

CATTLE | BEEF | BOS INDICUS | BOS TAURUS | BOVINE | BUFFALO | BULL | BULLOCK | CALF | COW | DAIRY COW | HEIFER | STEER

Ārstniecības joma:

IMMUNOTHERAPY

Ārstēšanas norādes:

BOVINE EPHEMERAL FEVER (BEF) | VACCINE | EQUINE ROTAVIRUS | THREE DAY SICKNESS

Produktu pārskats:

Poison schedule: 3; Withholding period: WHP: Zero (0) days ESI: Zero (0) days; Host/pest details: CATTLE: [BOVINE EPHEMERAL FEVER (BEF), VACCINE]; Poison schedule: 4; Withholding period: WHP: Nil; Host/pest details: CATTLE: [BOVINE EPHEMERAL FEVER (BEF), VACCINE]; Poison schedule: 4; Withholding period: ; Host/pest details: CATTLE: [BOVINE EPHEMERAL FEVER (BEF), VACCINE]; For the prevention of bovine ephemeral fever (3 day sickness) in cattle.

Autorizācija statuss:

Registered

Autorizācija datums:

2023-07-01

Lietošanas instrukcija

Product Name:
APVMA Approval No:
ULTRAVAC BEF VACCINE
41461/131429
Label Name:
ULTRAVAC BEF VACCINE
Signal Headings:
FOR ANIMAL TREATMENT ONLY
Constituent
Statements:
Bovine Ephemeral Fever Standard Strain (BB2271-919) at ≥
10^4.3TCID50/ 2 mL dose
Claims:
For the prevention of Bovine Ephemeral Fever (3 day sickness) in
cattle
Net Contents:
10 x 10 doses vaccine
10 x 20 mL diluent
1 x 10 dose vaccine
1 x 20 mL diluent
Directions for Use:
Restraints:
Contraindications:
Precautions:
Side Effects:
Following vaccination with this product, a transient febrile response
in animals may be
observed. This response could contribute to a sudden drop in milk
production by affected
dairy cattle.
Dosage and
Administration:
USE ALL RECONSTITUTED PRODUCT IMMEDIATELY.
2 mL dose by subcutaneous injection.
Primary vaccination: Cattle require an initial 2 mL dose
subcutaneously. The second 2 mL
subcutaneous dose can be effectively administered any time from 2
weeks up to 6 months
later.
Cattle can be vaccinated from 6 months of age. Two doses of vaccine
are required to
produce long lasting immunity. RLP APPROVED
Booster vaccination: 2 mL annual booster dose is required for all
cattle.
Preparation of the vaccine:
1. Draw up 2 mL of Ultravac BEF Diluent into a sterile syringe.
2. Add to the freeze dried vaccine in the small vial.
3. Draw up reconstituted vaccine into the syringe.
4. Transfer reconstituted vaccine into the Ultravac BEF Diluent
bottle.
5. Gently shake the diluent bottle to evenly distribute the vaccine
(excessive shaking will
cause foaming).
6. Reconstituted vaccine is orange in colour and must be used as soon
as possible.
General Directions:
NOTE: Equipment, syringes, needles used for vaccination must be clean,
sterile and free of
chemicals. After use, dismantle and wash in disinfectant such as
household bleach (20 mL
in 500 mL water) then rinse in cold water.
Withholding Periods:
Zero (0) days
Trade Advice:
Export Slaughter Interval (ESI): Zero (0) days
Safety Directions:
First Aid Instructions:
If poisoning occurs, c

Produkta apraksts

PRODUCT NAME: ULTRAVAC BEF VACCINE
PAGE: 1 OF 5
This version issued: 8 December 2014
SAFETY DATA SHEET
Issued by: Zoetis Australia Pty Ltd
Phone: [phone]
POISONS INFORMATION CENTRE: 13 1126 FROM ANYWHERE IN AUSTRALIA
SECTION 1 - IDENTIFICATION OF THE SUBSTANCE/MIXTURE AND SUPPLIER
ZOETIS AUSTRALIA PTY LTD
ABN 94 156 476 425
Level 6, 5 Rider Blvd
Rhodes NSW 2138 AUSTRALIA
Tel: [phone]
Fax: [phone]
Email: [e-mail]
CHEMICAL NATURE:
Freeze dried live viruses.
TRADE NAME:
ULTRAVAC BEF VACCINE
OTHER NAMES:
Ultravac BEF
APVMA APPROVAL NUMBER:
41461
RECOMMENDED USE:
For the prevention of bovine ephemeral fever by vaccination in cattle.
RESTRICTIONS ON USE
For veterinary use only.
EMERGENCY PHONE:
1800 814 883 (ALL HOURS)
CREATION DATE:
SEPTEMBER, 2014
THIS VERSION ISSUED:
DECEMBER, 2014
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.
Not a Dangerous Good according to Australian Dangerous Goods (ADG)
Code, IATA and IMDG/IMSBC criteria.
RISK PHRASES:
Not Hazardous - No criteria found.
SAFETY PHRASES:
Not Hazardous - No criteria found.
SUSMP CLASSIFICATION:
S4
ADG CLASSIFICATION:
None allocated. Not a Dangerous Good under the ADG Code.
UN NUMBER:
None allocated
GHS CLASSIFICATION:
GHS LABEL ELEMENTS: NONE. NOT HAZARDOUS.
SIGNAL WORD: NONE. NOT HAZARDOUS.
HAZARD STATEMENT: NONE. NOT HAZARDOUS.
PREVENTION
P102: Keep out of reach of children.
P235: Keep cool, preferably between 2 and 8°C, but do not freeze.
P262: Do not get in eyes, on skin, or on clothing.
P281: Use personal protective equipment as required.
RESPONSE
P353: Rinse skin or shower with water.
P301+P330+P331: IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.
P370+P378: Not combustible. Use extinguishing media suited to burning
materials.
STORAGE
P402+P404: Store in a dry place. Store in a closed container.
DISPOSAL
P501: Discarded vials/containers should immediately be pla