PRODUCT NAME
CLAMOX RTU 100 ML
Composition:
Each ml of product contains 140 mg Amoxicillin (as Amoxicillin Trihydrate) and Clavulanic Acid 35 mg (as Potassium Clavulanate).
TARGET SPECIES
Cattle, pigs, dogs and cats.
INDICATIONS
The product is indicated in cattle, pigs, dogs and cats for the treatment of infections caused by germs sensitive to the action of active substances.
Cattle – Respiratory infections, soft tissue infections (abscesses, arthritis), metritis and mastitis.
Swine – Respiratory infections. Colibacillosis.
Dogs and cats – Urinary tract infections, respiratory tract infections, skin and soft tissue infections (abscesses, pyodermatitis, perianal gland abscesses, gingivitis).
CONTRAINDICATIONS
Do not use in case of hypersensitivity to the active substance or to any of the excipients. The product should not be given to rabbits, guinea pigs and hamsters. It should be used with caution on other small herbivores.
SIDE EFFECTS
Occasionally, the product may cause reactions at the site of inoculation and/or local tissue reactions.
DOSAGE FOR EACH SPECIES, ROUTE(S) OF ADMINISTRATION AND METHOD OF ADMINISTRATION
It can be administered subcutaneously or intramuscularly in dogs and cats and intramuscularly in cattle and pigs.
The dose is 8.75 mg/kg body weight equivalent to 1 ml of product/20 kg body weight repeated every 24 hours for 3 to 5 days.
The bottle will be shaken very well before use. After the injection, the injection site will be massaged. A completely dry sterile syringe and needle will be used.
Combination therapy for the treatment of mastitis in cattle: if a general treatment is required in addition to intramammary treatment, Clamox RTU can be used in combination with Clamox LC.
WARNINGS / RECOMMENDATIONS FOR CORRECT ADMINISTRATION
To ensure correct dosing and to avoid underdosing, the body weight of animals must be determined as accurately as possible.
WAITING TIME
Cattle (meat and offal) 28 days
Pigs (meat and offal) 19 days
Milk 48 hours
In the case of combination therapy, the milk will be given for consumption after 60 hours from the last treatment (after 5 milkings, if the cows are milked twice a day).
VALIDITY PERIOD
Shelf life of the veterinary medicinal product as packaged for sale: 2 years.
Shelf life after the first opening of the immediate packaging: 28 days.
SPECIAL PRECAUTIONS FOR STORAGE
Do not store at temperatures above 25 °C.
It will protect itself from light.
SPECIAL PRECAUTIONS FOR USE IN ANIMALS
The use of the product must be based on testing the susceptibility of bacteria isolated from animals. If this is not possible, therapy should be based locally on epidemiological information about the susceptibility of the target bacteria. Use of the product outside of the instructions provided in the SPC may increase the prevalence of resistant bacteria and decrease the effectiveness of the treatment due to the potential for cross-resistance.
SPECIAL PRECAUTIONS FOR PERSONNEL ADMINISTERING THE PRODUCT
Penicillins and cephalosporins may cause hypersensitivity (allergy) reactions after self–injection, inhalation, ingestion or skin contact. Hypersensitivity to penicillins may be associated with cross–sensitivity to cephalosporins and vice versa. Occasionally, allergic reactions to these substances can be serious.
In the case of accidental self–injection, seek the advice of the doctor to whom the leaflet or label of the product will be presented. In case of accidental contact with the skin, wash with soap and water.
This product should be handled with great care to prevent exposure by ensuring all precautions.
Do not handle this product if you know that you are a sensitive person or have been warned not to handle such preparations.
This product will be handled with great care to prevent exposure by ensuring all precautions.
If symptoms occur as a result of exposure to this product, such as: itchy skin, you should immediately consult a doctor and present this warning to your doctor.
Swelling of the face, lips or eyes or difficulty breathing are much more serious symptoms and require immediate medical attention.
USE DURING PREGNANCY, LACTATION OR LAYING
The product can be used in pregnant animals or during the lactation period.
INTERACTIONS WITH OTHER MEDICINAL PRODUCTS OR OTHER FORMS OF INTERACTION
It should not be administered concomitantly with bacteriostatic antibiotics that are incompatible.
OVERDOSE
Amoxicillin has a low toxicity and is well tolerated when administered parenterally.
With the exception of occasional local administration site reactions, which may occur even at the recommended dose, no other adverse effects have been observed even with accidental overdose.
INCOMPATIBILITIES
In the absence of compatibility studies, this medicinal product should not be mixed with other veterinary medicinal products.
SPECIAL PRECAUTIONS FOR DISPOSAL OF UNUSED PRODUCT OR WASTE, AS APPROPRIATE
Any unused veterinary medicinal product or waste from the use of such a product should be disposed of in accordance with local requirements.
Medicines should not be disposed of in wastewater or household waste.
PRESENTATION/PACKAGING
100 ml high-density polypropylene bottles, closed with brombutyl rubber stopper and aluminium staple.
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