国家: 澳大利亚
语言: 英文
来源: APVMA (Australian Pesticides and Veterinary Medicines Authority)
MYCOBACTERIUM PARATUBERCULOSIS; THIOMERSAL
ZOETIS AUSTRALIA PTY LTD
M. paratuberculosis(2.5mg/mL)
MISC. VACCINES OR ANTI SERA
MYCOBACTERIUM PARATUBERCULOSIS VACCINE Active 2.5 mg/ml; THIOMERSAL MERCURY Other 0.1 mg/ml
100mL; 250mL
VM - Veterinary Medicine
ZOETIS AUSTRALIA
GOAT | SHEEP | BILLY | BUCK | CAPRA HIRCUS | DOE | EWE | HOGGET | KID | LAMB | OVINE | RAM | WEANER | WETHER
IMMUNOTHERAPY
JOHNE'S DISEASE | MYCOBACTERIUM PARATUBERCULOSIS SHEDDING
Poison schedule: 0; Withholding period: WHP:(Meat Milk):Nil; Host/pest details: GOAT: [JOHNE'S DISEASE]; SHEEP: [JOHNE'S DISEASE, MYCOBACTERIUM PARATUBERCULOSIS SHEDDING]; Poison schedule: 0; Withholding period: ; Host/pest details: GOAT: [JOHNE'S DISEASE]; SHEEP: [JOHNE'S DISEASE, MYCOBACTERIUM PARATUBERCULOSIS SHEDDING]; Active immunisation for the control of Johne's disease and reduction in faecal Mycobacterium paratuberculosis shedding in sheep. Active immunisation as an aid in the control of Johne's disease in goats.Do not vaccinate sheep or goats younger than 1 month. NOTE: VACCINATED ANIMALS ARE LIKELY TO GIVE POSITIVE RESULTS WHEN TESTED FOR TUBERCULOSIS OR JOHNE'S DISEASE.
Registered
2023-07-01
AUSTRALFAN GOVERNMENT AUSTRALIAN PESTICIDES AND VETERINARY MEDICINES AUTHORITY RLP APPENDIX 2 Approved TEMPLATE FOR RELEVANT LABEL PARTICULARS (RLPS) (VETERINARY PRODUCTS) Select appropriate: [J New Product (include all applicable RLPs) OR X Variation (highlight instructions that are being varied). Approval no. of label being varied: 53839/0808 Signal heading: Product name: Active constituent/s: Statement of claims: Net contents: Directions for Use Heading: READ SAFETY DIRECTIONS FOR ANIMAL TREATMENT ONLY Gudair® Vaccine This vaccine contains a suspension of the microorganism, Mycobacterium avium subsp. paratuberculosis, strain 316F, inactivated by heat and adjuvanted with mineral oil in a multiple emulsion. It contains 2.5 mg of dried microorganisms per ml Additional Constituent: Thiomersal 0.1 mg/ml as preservative Active immunisation for the control of Johne's disease and reduction in faecal Mycobacterium avium subsp. paratuberculosis shedding in sheep. Active immunisation as an aid in the control of Johne's disease in goats. INDICATIONS FOR USE GUDAIR® VACCINE is indicated for the control of Johne's disease in sheep, and as an aid in the control of Johne's disease in goats. Transmission of Mycobacterium avium subsp. paratuberculosis in sheep and goats is primarily by the faecal-oral route. The bacteria enter through the Peyer's patches of the small intestine and infect the terminal ileum, caecum, colon and associated mesenteric lymph nodes and vessels. Johne's disease has a prolonged incubation period with clinical disease, characterised by weight loss and emaciation, most commonly seen in sheep older than two years of age. About 1 0% of clinical cases show diarrhoea in the end stage of the disease. Some animals become carriers of the infection, intermittently shedding the bacteria into their environment. These subclinical carriers can develop into active clinical cases which usually die from malabsorption. Milk production in infected sheep and goats is reduced and wool break and poor fleece condition have 阅读完整的文件
PRODUCT NAME: GUDAIR® VACCINE PAGE: 1 OF 6 This revision issued: 24 th September, 2014 SAFETY DATA SHEET Issued by: Zoetis Australia Pty Ltd Phone: 1800 814 883 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: 1800 814 883 Fax: (02) 8876 0444 Email: australia.animalhealth@zoetis.com PRODUCT IDENTIFIER: GUDAIR ® VACCINE OTHER NAMES: None. CHEMICAL FAMILY: Oil-water emulsion with vaccine and other minor ingredients. APVMA APPROVAL NUMBER: 53839 PRODUCT USE: Animal vaccine for use as described on the product label for the control of Johne’s Disease in sheep and goats. RESTRICTIONS ON USE For veterinary use only. EMERGENCY PHONE: 1800 814 883 (ALL HOURS) 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 or IMDG/IMSBC criteria. RISK PHRASES: Not Hazardous - No criteria found. SAFETY PHRASES: S23, S36, S24/25. Do not breathe vapours or mists. Wear suitable protective clothing. Avoid contact with skin and eyes. ADG CLASSIFICATION: None allocated. Not a Dangerous Good according to Australian Dangerous Goods (ADG) Code, IATA or IMDG/IMSBC criteria. GHS CLASSIFICATION: NOT HAZARDOUS. GHS LABEL ELEMENTS: NONE. NOT HAZARDOUS. SIGNAL WORD: NONE. NOT HAZARDOUS. PREVENTION P102: Keep out of reach of children. P262: Do not get in eyes, on skin, or on clothing. P281: Use personal protective equipment as required. RESPONSE P352: Wash with plenty of soap and water. P301+P330+P331: IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. P370+P378: Not combustible. Use extinguishing media suited to burning materials. STORAGE P410: Protect from sunlight. P411: Store between 2°C and 8°C (refrigerate, do not freeze). DISPOSAL P501: Dispose of small quantities and empty containers 阅读完整的文件