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Date: Monday, May 6, 2024 22:52

Release 2.70
Multiject IMM Intramammary Suspension
 
Species: Cattle
Therapeutic indication: Pharmaceuticals: Antimicrobials: Intramammaries: Lactating cow
Active ingredient: Neomycin Sulfate, Prednisolone, Procaine Benzylpenicillin, Streptomycin Sulfate
Product:Multiject IMM Intramammary Suspension
Product index: Multiject Intramammary
Cattle - milk: 108 hours
Cattle - meat: 7 days
Incorporating:
Qualitative and quantitative composition
Each 5g syringe contains:
Active substance(s):
Procaine Benzylpenicillin
100,000 IU
Streptomycin Sulfate
100 mg
Neomycin Sulfate
100 mg
Prednisolone
10 mg
For a full list of excipients, see section Pharmaceutical Particulars
Pharmaceutical form
Intramammary suspension.
A white oily suspension.
Clinical particulars
Target species
Cattle (milk cows).
Indications for use, specifying the target species
Indicated in the treatment of acute and subacute bovine mastitis in milking cows, accompanied by pain and inflammation caused by bacterial infection sensitive to penicillin, streptomycin and neomycin therapy.
Contraindications
None.
Special Warnings for each target species
No special warnings.
Special precautions for use
Special precautions for use in animals
During a course of treatment the situation should be reviewed frequently by close veterinary supervision.
Special precautions to be taken by the person administering the veterinary medicinal product to animals
Protective gloves should be worn when infusing heifers, to avoid skin contact with the product.
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 this product if you know you are sensitised, or if you have been advised not to work with such preparations.
Handle this product with great care to avoid exposure, taking all recommended precautions.
If you develop symptoms following exposure such as skin rash, you should seek medical advice and show the doctor this warning. Swelling of the face, lips or eyes or difficulty with breathing are more serious symptoms and require urgent medical attention.
Wash hands after use.
Adverse reactions (frequency and seriousness)
No known undesirable effects.
Use during pregnancy, lactation or lay
This product can be safely administered to cows during pregnancy or lactating. Also see warning in section, "Withdrawal period" regarding withdrawal periods.
Interaction with other medicinal products and other forms of interaction
None known
Amounts to be administered and administration route
The contents of one syringe should be infused gently into each infected quarter via the teat canal immediately after milking, once daily for three consecutive days. Aseptic precautions should be observed at all times.
Overdose (symptoms, emergency procedures, antidotes), if necessary
Not applicable.
Withdrawal period
Milk for human consumption must not be taken from a cow during treatment. Milk for human consumption may only be taken from 108 hours from the last treatment.
Animals must not be slaughtered for human consumption during treatment. Cattle may be slaughtered for human consumption only after 7 days from the last treatment.
Pharmacological particulars
Pharmacotherapeutic group: Antibacterials for intramammary use, Combination of antibacterials for intramammary use, Combinations of antibacterials and other substances.
ATCvet Code: QJ51RV01
Pharmacodynamic properties:
Procaine Penicillin exerts its effect on multiplying bacteria by interfering with the formation of the cell wall.
Streptomycin sulphate and Neomycin Sulphate are both aminoglycoside antibiotics which after penetration of the cell envelope bind to receptors on the 30s subunit of the ribosome. They induce misreading of the genetic code on the messenger ribonucleic acid (mRNA) template. Prednisolone is a glucocorticoid which has anti-inflammatory properties.
Pharmaceutical particulars
List of excipients
Liquid Paraffin Light
White Soft Paraffin
Incompatibilities
None known.
Shelf life
Shelf life of the veterinary medicinal product as packaged for sale: 2 years.
Special precautions for storage
Do not store above 25°C.
The syringe must only be used once. Part used syringes must be discarded.
Nature and composition of immediate packaging
White pre-filled 5g single dose intramammary syringes with a low density polyethylene barrel and white or yellow plunger, with white or yellow low density polyethylene end caps.
Available in packs of 24 single dose syringes.
Special precautions for the disposal of unused veterinary medicinal product or waste materials
Any unused veterinary medicinal product or waste material derived from such veterinary medicinal products should be disposed of in accordance with local requirements.
Marketing Authorisation Holder (if different from distributor)
Norbrook Laboratories Limited, Station Works, Newry, Co. Down, BT35 6JP Northern Ireland
Marketing Authorisation Number
Vm 02000/4062
Significant changes
Date of the first authorisation or date of renewal
29th March 1985
Date of revision of the text
July 2010
Any other information
Nil.
Legal category
Legal category: POM-V
GTIN
GTIN description:Multiject IMM 24x 5g
GTIN:5023534001171