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Package Insert Summary
Formula:
Each 100 mL contains:
Oxytetracycline (hydrochloride)………………………………………………………….. 20.0 g
Sodium diclofenac.............................................................................. 1.0 g
Vehicle q.s.p. ………………………………………………………………………..100ml
Recommendation:
OXITRAT LA PLUS is indicated to combat infections caused by Gram positive and Gram negative bacteria susceptible to oxytetracycline, as well as in the treatment of anaplasmosis in cattle.
Dosage and Route of Administration:
Intramuscular route: The recommended dosage is 1.0 mL/10 kg of body weight, which corresponds to 20 mg of oxytetracycline/kg of weight and 1.0 mg of sodium diclofenac/kg of weight for cattle.
Intravenous route: The recommended dosage is 1.0 mL/20 kg of body weight, which corresponds to 10 mg of oxytetracycline/kg of weight and 0.5 mg of diclofenac sodium/kg of weight for cattle.
Interval between doses:
Intramuscular route: normally one dose is sufficient for an effective treatment, however in severe infections, a second dose must be administered 3 days after the first application. Intravenous use: administer a second dose 24 hours after the first application and repeat for a maximum of 4 consecutive days.
Recommended maximum volume per application point is: 10 mL.
Doses higher than those indicated above, administered intramuscularly, should be subdivided into two or more points of application.
Underdosing can facilitate the development of resistance and interfere with the effectiveness of the treatment.
Contraindications:
It is contraindicated for use in horses, dogs and cats;
Although the antibiotic is well tolerated, occasionally small local reactions (mild edema) of a transient nature may be observed.
Withdrawal Period: cattle: slaughter: The slaughter of animals treated intravenously or intramuscularly should only be carried out 39 days after the last application. milk: Milk from animals treated intravenously should not be destined for human consumption until 07 days after the last application of this product. Milk from animals treated by the intramuscular route should not be destined for human consumption until 19 days after the last application of this product.
Presentation: Vial-ampoule containing 50 mL and 100 mL.
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