Ubrostar Dry Cow Intramammary Suspension For Cattle
Revised: July 2014
NAME OF THE VETERINARY MEDICINAL PRODUCT
Ubrostar Dry Cow Intramammary Suspension for cattle
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each 4.5g intramammary syringe contains:
Penethamate Hydriodide 100 mg (equivalent to 77.2 mg penethamate)
Benethamine Penicillin 280 mg (equivalent to 171.6 mg penicillin)
Framycetin Sulphate 100 mg (equivalent to 71.0 mg framycetin)
For a full list of excipients, see section 6.1.
White to off white suspension.
Cattle (at dry off)
Indications for use, specifying the target species
For treatment of subclinical mastitis at drying off, and the prevention of new bacterial infections of the udder during the dry period in dairy cows, caused by bacteria susceptible to penicillin and framycetin.
Do not use in lactating cows.
Do not use in case of hypersensitivity to the active substances or to any of the excipients.
Where there is a risk of summer mastitis, additional management procedures, such as fly control should be considered.
Special precautions for use
Special precautions for use in animals
Use of the product should be based on susceptibility testing of the bacteria isolated from the animal. If this is not possible, therapy should be based on local (regional, farm level) epidemiological information about susceptibility of the target bacteria. Official and local antimicrobial policies should be taken into account when the product is used.
Special precautions to be taken by the person administering the veterinary medicinal product to animals
Skin sensitisation may occur in persons handling the product; care should be taken to avoid contact with skin.
Penicillins and cephalosporins may cause hypersensitivity following injection, inhalation, ingestion or skin contact. Hypersensitivity to penicillins may lead to cross reactions to cephalosporins and vice versa. Allergic reactions to these substances may occasionally be serious.
Do not handle the product if you know that you are sensitised, or if you have been advised not to work with such preparations.
Handle this product with care (especially persons with skin damage) to avoid exposure. Wear gloves, wash hands in case of contact with skin.
If you develop symptoms such as a skin rash following exposure, seek medical advice and show this warning to your doctor. Swelling of the face, lips or eyes, or difficulty breathing are more serious symptoms and require urgent medical attention.
Adverse reactions (frequency and seriousness)
Use during pregnancy, lactation or lay
Pregnancy: Can be used during pregnancy.
Lactation: Do not use during lactation.
Interaction with other medicinal products and other forms of interaction
Amounts to be administered and administration route
Intramammary administration of 100 mg penethamate hydriodide, 280 mg benethamine penicillin and 100 mg framycetin sulphate into each quarter, i.e. the contents of one syringe to be infused into each quarter immediately after the last milking of a lactation.
Before infusion, the teats should be thoroughly cleaned and disinfected, and care should be taken to avoid contamination of the injector nozzle. Following infusion, it is advisable to use a teat wipe or spray.
Overdose (symptoms, emergency procedures, antidotes), if necessary
Meat and offal: 10 days
Milk: If treated at least 35 days before calving, milk must not be used for 36 hours after calving.
If treated less than 35 days before calving, milk must not be used for 37 days after treatment.
Pharmacotherapeutic group:Antibacterials for intramammary use, Combination of antibacterials for intramammary use, Beta-lactam antibacterials, penicillins, combinations with other antibacterials
Benethamine benzylpenicillin is the N-benzyl-2phenylethylamine salt of benzylpenicillin, designed as a long-acting formulation of benzylpenicillin. Penethamate is a prodrug from which benzylpenicillin and diethylaminoethanol are released by hydrolysis. Antimicrobial activity is derived exclusively from benzylpenicillin.
The free benzylpenicillin is effective chiefly against a variety of gram-positive pathogens, excluding β-lactamase producing staphylococci. Penicillins act bactericidally on proliferating micro-organisms by inhibiting cell wall synthesis. The antibacterial activity is time dependent.
Framycetin, also known as neomycin B, is a bactericidal aminoglycoside antibiotic. Inhibition of bacterial protein synthesis and presumed interference with permeability at the cell membrane play a role in effecting bacterial cell death. Its action spectrum encompasses numerous gram-negative and some gram-positive bacteria.
In vitroefficacy has been demonstrated against: Staphylococcus spp., Streptococcus spp., Arcanobacterium spp. (Corynebacterium spp.), Escherichia coli, Klebsiella spp.and Pseudomonas spp.
The penicillin components of the product will remain in the dry udder for up to 3 weeks. In the majority of cows the framycetin components will remain in the dry udder for 10 weeks, or until calving.
List of excipients
Castor oil, hydrogenated
Shelf-life of the veterinary medicinal product as packaged for sale: 3 years.
Special precautions for storage
Do not store above 25 C
Nature and composition of immediate packaging
Cardboard box or plastic container containing 20 or 60 single use intramammary syringes and 20 or 60 teat wipes (containing isopropanol 70 %).
Each 4.5 g syringe (cylinder with piston and cap, all made of low density polyethylene) contains 5 ml intramammary suspension.
Not all pack sizes may be marketed.
Special precautions for the disposal of unused veterinary medicinal product or waste materials derived from the use of such products
Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal product should be disposed of in accordance with local requirements.
MARKETING AUTHORISATION HOLDER
Boehringer Ingelheim Limited
MARKETING AUTHORISATION NUMBER
DATE OF FIRST AUTHORISATION
Date:13 December 2011
DATE OF REVISION OF THE TEXT
25 July 2014
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