MICROAMOX
Compositions:
1000 g of premix contains: Amoxicillin trihydrate equal to amoxicillin 300 g; Excipients q.s. to 1000 g
Pharmaceutical form: premix
Indications: Local and septicaemic infections sustained by amoxicillinsensible Gram-positive and Gram-negative bacteria in particular: respiratory disease caused by Actinobacillus pleuropneumoniae and Pasteurella multocida, streptococcosis by Streptococcus suis.
Contraindications: Sensitivity to penicillin and cephalosporines.
Adverse reactions: None known. If you notice any serious effects or other effects not mentioned in this leaflet, please inform your veterinary surgeon.
Target species: pigs
Method and route of administration: Administer MICROAMOX accurately mixed to the feed, at the dose of 1250 – 1500 g every ton of complete feed, depending on the body weight and daily feed intake, in order to achieve a daily dose rate of 15 mg/kg b.w / day of amoxicillin. In subjects on rationed diet, the dose of premix in the feed must be increased according to body weight and daily feed intake.
Feed consumption |
Kg of premix/ ton of complete feed |
1% |
5 kg |
3% |
1.66 kg |
5% |
1 kg |
Follow the therapy for 5 days.
Withdrawal periods: Meat and offal: 7 days.
Special storage conditions: This veterinary medicinal product does not require any special storage precaution, apart from those required
for a correct storage of drugs. Close again the packaging after the use
Special warnings: Amoxicillin must not be administered to guinea pigs or rabbits.
Special warnings for each target species: None
Special precautions for use in animals: None
Special precautions to be taken by the person administering the veterinary medicinal product to animals:
Amoxicillin may provoke allergic sensibilization in man if swallowed, inhaled or brought into contact. Such reactions may lead to serious anaphylactic shock. The product must not be handled by persons known to be sensitive to beta-lactamic. The product should be handling with caution; it must be avoided swallow, inhale and contact by wearing protective clothes, masks, waterproof gloves and eyeglasses. Skin-rash, face swelling and breathing difficulties require
urgently the presence of the doctor.
Use during pregnancy, lactation: Do not use during lactation. None teratogenic or embryotoxic effect of amoxicillin are known. Use in pregnancy only accordingly to the beneft/ risk assessment by the responsible veterinary.
Interactions with other medicinal products and other forms of interaction: The product should not be administered concomitantly with drugs having a bacteriostatic action.
Overdose (symptoms, emergency procedures, antidotes), if necessary: Amoxicillin is well tolerated when administered orally, even in doses higher than those prescribed. Allergic reactions arising when the product is administered to sensitive subjects must be treated promptly with adrenalin and cortisone preparations.
Incompatibilities: None known
SPECIFIC PRECAUTIONS FOR THE DISPOSAL OF UNUSED PRODUCT OR WASTE MATERIALS IF ANY:
Any unused veterinary medicinal product or waste materials derived from such medicinal products should be disposed of in accordance with local requirements.
Shelf-life: 24 months
Shelf-life after frst opening the immediate packaging: 3 months
Shelf-life after incorporation into feed: 6 months
Presentations: bag of 10 kg and 25 kg
FOR VETERINARY USE ONLY
Keep out of the reach of children
Industria Italiana Integratori TREI S.p.A
42010 Rio Saliceto (RE) Italy - Via Affarosa, 4