দেশ: অস্ট্রেলিয়া
ভাষা: ইংরেজি
সূত্র: APVMA (Australian Pesticides and Veterinary Medicines Authority)
CEFUROXIME SODIUM
AVET HEALTH LIMITED
cefuroxime sodium(92.2g/kg)
MISC. INTRA MAMMARY
CEFUROXIME SODIUM ANTIBIOTIC Active 92.2 g/kg
20x3g; 3g syringe
VM - Veterinary Medicine
DAIRY CATTLE | BOVINE | BREEDERS | CALVES | DAIRY COW | GROWERS | LACTATING COW | MILKING COW
ANTIBIOTIC & RELATED
CITROBACTER FREUNDII SPP. | CORYNEBACTERIA | ENTEROBACTER SPP. | ESCHERICHIA COLI (E. COLI) | KLEBSIELLA SPP. | MASTITIS | MICROCOCCUS SPP. | STAPHYLOCOCCUS AUREUS | STAPHYLOCOCCUS SPP. | STREPTOCOCCUS AGALACTIAE | STREPTOCOCCUS DYSGALACTIAE | STREPTOCOCCUS UBERIS | INCLUDING B-LACTAMASE PRODUCIN | STAPHYLOCOCCOSIS | SUBCLINICAL MASTITIS
Poison schedule: 4; Withholding period: MEAT: DO NOT USE less than 7 days before slaughter for human consumption. MILK: Milk taken from cows within 72 hours (6 milkings) following last treatment MUST NOT BE USED for human consumption or su pplied for processing. This milk should not be fed to bobby calves. ESI: This product does not have an ESI establishe d. For advice on the ESI contact Jurox P ty Ltd on 1800 023 312 before using this product.; Host/pest details: DAIRY CATTLE: [CITROBACTER FREUNDII SPP., CORYNEBACTERIA, ENTEROBACTER SPP., ESCHERICHIA COLI (E. COLI), KLEBSIELLA SPP., MASTITIS, MICROCOCCUS SPP., STAPHYLOCOCCUS AUREUS, STAPHYLOCOCCUS SPP., STREPTOCOCCUS AGALACTIAE, STREPTOCOCCUS DYSGALACTIAE, STREPTOCOCCUS UBERIS]; Poison schedule: 4; Withholding period: WHP: MEAT: DO NOT USE less than 7 days before slaughter for human consumption . MILK: Milk taken from cows within 72 hours (6 milkings) following last trea tment MUST NOT BE USED for human consum ption or supplied for processing. This milk should not be fed to bobby calves. ESI: This product does not have an ESI established. For advice on the ESI co ntact Jurox Pty Ltd on 1800 023 312 be fore using this product.; Host/pest details: DAIRY CATTLE: [CITROBACTER FREUNDII SPP., CORYNEBACTERIA, ENTEROBACTER SPP., ESCHERICHIA COLI (E. COLI), KLEBSIELLA SPP., MASTITIS, MICROCOCCUS SPP., STAPHYLOCOCCUS AUREUS, STAPHYLOCOCCUS SPP., STREPTOCOCCUS AGALACTIAE, STREPTOCOCCUS DYSGALACTIAE, STREPTOCOCCUS UBERIS]; Poison schedule: 4; Withholding period: ; Host/pest details: DAIRY CATTLE: [CITROBACTER FREUNDII SPP., CORYNEBACTERIA, ENTEROBACTER SPP., ESCHERICHIA COLI (E. COLI), KLEBSIELLA SPP., MASTITIS, MICROCOCCUS SPP., STAPHYLOCOCCUS AUREUS, STAPHYLOCOCCUS SPP., STREPTOCOCCUS AGALACTIAE, STREPTOCOCCUS DYSGALACTIAE, STREPTOCOCCUS UBERIS]; For broad spectrum control of mastitis causing bacteria (including penicillin resistant strains) in lactating dairy cattle.Milk for human consumption must not be taken from a cow during treatment. Milk taken from cows within 72 hours (6 milkings) following last treatment must NOT be fed to bobby calves.
Registered
2023-07-01
elevet+ MAXALAC L.C. INTRAMAMMARY ANTIBIOTIC 59528/139099 Product Name: APVMA Approval No : Label Name: elevet+ MAXALAC L.C. INTRAMAMMARY ANTIBIOTIC Signal Headings: PRESCRIPTION ANIMAL REMEDY KEEP OUT OF REACH OF CHILDREN FOR ANIMAL TREATMENT ONLY Constituent Statements: 92.2 g/kg CEFUROXIME SODIUM (250 mg/3 g syringe CEFUROXIME) Claims: For broad spectrum control of mastitis-causing bacteria (including penicillin resistant strains) in lactating dairy cattle. Net Contents: 20 x 3 g syringe 3 g syringe Directions for Use: Restraints: Milk for human consumption must not be taken from a cow during treatment. Contraindications: Precautions: Side Effects: Dosage and Administration: Use elevet+ Maxalac L.C. Intramammary Antibiotic as directed by your veterinary surgeon as part of a mastitis control program. Wear gloves when infusing the treatment. Before infusion the teat should be thoroughly cleaned and disinfected. The contents of one syringe should be infused into the teat canal of each infected quarter every 12 hours, after each of three successive milkings. RLP APPROVED Administration 1. After milking is complete, thoroughly clean and disinfect the end of the teat (e.g. with cotton wool soaked in alcohol). 2. Hold the barrel of the syringe firmly in one hand and gently twist and pull the protective cap in a straight line to remove it, taking care not to contaminate the nozzle. 3. Insert the nozzle fully into the teat canal and apply steady pressure on the syringe plunger until the full dose has been delivered. Holding the end of the teat with one hand, gently massage upwards with the other to aid dispersion of the antibiotic into the quarter. 4. After infusion it is advisable to dip the teats in an antiseptic preparation specifically designed for this purpose. Any variation by the prescribing veterinarian to the approved dose, frequency, duration, route, disease or target species may require extending the approved withholding period. General Directions: Indications elevet+ Maxalac L.C. Intramammary Antibiotic is সম্পূর্ণ নথি পড়ুন
MAXALAC LC INTRAMAMMARY Page 1 of 5 continued ISSUED: 3 OCTOBER 2012 SAFETY DATA SHEET SECTION 1: IDENTIFICATION OF CHEMICAL PRODUCT AND COMPANY PRODUCT NAME: MAXALAC LC INTRAMAMMARY ANTIBIOTIC PRODUCT CODE: 503205 (20 x 3g syringes) RECOMMENDED USE: An intramammary infusion to treat mastitis in lactating cows. COMPANY IDENTIFICATION: Jurox Pty Limited ADDRESS: 85 Gardiner Street Rutherford NSW 2320 Australia CUSTOMER CENTRE: 1800 023 312 NATIONAL POISONS INFORMATION CENTRE: 131126 (Australia-wide) EMERGENCY TELEPHONE NUMBER: 1800 023 312 (9a.m. – 5p.m.) SECTION 2: HAZARDS IDENTIFICATION GHS HAZARD CLASSIFICATIONS: RESPIRATORY SENSITIZER CATEGORY 1 SKIN SENSITIZER CATEGORY 1 GHS PICTOGRAMS: HEALTH HAZARD EXCLAMATION MARK SIGNAL WORD*: DANGER HAZARD STATEMENTS*: H317 May cause an allergic skin reaction. H334 May cause allergy or asthma symptoms or breathing difficulties if inhaled. PRECAUTIONARY STATEMENTS*: PREVENTION P261 Avoid breathing vapours. P272 Contaminated work clothing should not be allowed out of the workplace. P280 Wear protective gloves/protective clothing/eye protection/face protection. P285 In case of inadequate ventilation wear respiratory protection. RESPONSE P302+P352 IF ON SKIN: Wash with plenty of soap and water. P304+P341 IF INHALED: If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing. P333+P313 If skin irritation or rash occurs: Get medical advice. P342+P311 If experiencing respiratory symptoms: Call a POISON CENTER or doctor. P363 Wash contaminated clothing before reuse. DISPOSAL P501 Dispose of contents / container in accordance with local / national regulations. * N.B.: These statements are determined by Work Health and Safety regulations and may not reflect Signal Headings and First Aid and Safety statements on product labelling, which are determined by a competent authority during assessment for registration. MAXALAC LC INTRAMAMMARY Page 2 of 5 continued SECTION 3: COMPOSITION / INFORMATION ON INGREDIENTS INGREDIENT CAS NO. CO সম্পূর্ণ নথি পড়ুন
WWW.JUROX.COM.AU Customer Service 1800 023 312 ® Registered Trademark of Jurox Pty Limited TECHNICAL NOTES ACTIVE CONSTITUENT Each syringe contains 250 mg cefuroxime (as cefuroxime sodium) ACTIONS MAXALAC® L.C. is indicated for the treatment of clinical mastitis in milking cows. It is an intramammary infusion containing cefuroxime in a quick-release oily base. The base disperses readily in milk and allows rapid distribution of high levels of antibiotic in both milk and tissues of treated quarters. Cefuroxime sodium is a second generation, semi-synthetic cephalosporin antibiotic which is resistant to degradation by beta- lactamase enzymes produced by both Gram-positive and Gram-negative mastitis pathogens. INDICATIONS For the treatment of clinical mastitis caused by the following pathogens: _Staphylococcus spp., Staphylococcus aureus_, including penicillin resistant spp.,_ Streptococcus agalacatiae, Streptococcus dysgalactiae, Streptococcus uberis, Escherichia coli, Corynebacterium _spp. (including _Arcanobacterium pyogenes_). The antibiotic, cefuroxime, is also active against other organisms recovered from the bovine udder including _Klebsiella _spp.,_ Citrobacter _spp.,_ Enterobacter _spp_. and Micrococcus _spp. MAXALAC® L.C. is therefore suitable for the treatment of clinical mastitis caused by all the major mastitis pathogens. RESTRAINTS Milk for human consumption must not be taken from a cow during treatment. PRECAUTIONS Any variation by the prescribing veterinarian to the approved dose, frequency, duration, route, disease or target species may require extending the approved withholding period. Wear sanitised rubber gloves when applying. MAXALAC ® L.C. Intramammary Antibiotic WWW.JUROX.COM.AU Customer Service 1800 023 312 ® Registered Trademark of Jurox Pty Limited TECHNICAL NOTES WITHHOLDING PERIODS MILK: Milk taken from cows within 72 hours (6 milkings) following last treatment MUST NOT BE USED for human consumption or supplied for processing. This milk should not be fed to bobby calves. MEAT: DO NOT U সম্পূর্ণ নথি পড়ুন