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Antibiotic with anti-inflammatory and analgesic action.
COMPOSITION:
Each mL of injectable solution contains:
Oxytetracycline base 200 mg
Diclofenac sodium 5 mg
Excipients q.s. to 1 mL
INDICATIONS:
Indicated in cattle for the treatment of respiratory diseases, foot infections, and hemoparasitic diseases (anaplasmosis) caused by Anaplasma marginale, Pasteurella multocida, Fusobacterium necrophorum, Staphylococcus spp., and Streptococcus spp.
Also indicated as an adjunct in the management of pain, fever, and inflammation associated with these conditions.
DOSAGE AND ROUTE OF ADMINISTRATION:
Deep intramuscular injection.
General dosage: 1 mL per 10 kg body weight, equivalent to 20 mg of oxytetracycline base/kg and 0.5 mg of diclofenac sodium/kg.
Do not administer more than 10 mL per injection site.
WITHDRAWAL PERIOD:
Animals must not be slaughtered for human consumption until 28 days after the end of treatment.
Milk produced during treatment and for 6 days after must not be used for human consumption.
CONTRAINDICATIONS:
Do not administer concomitantly with other non-steroidal anti-inflammatory drugs (NSAIDs) or glucocorticoids.
Due to the calcium-binding capacity of tetracyclines, avoid use in growing animals and pregnant females.
PRECAUTIONS:
Keep out of reach of children and domestic animals.
Store at temperatures not exceeding 30°C.
Veterinary prescription only.
Dispose of empty containers or residual contents according to current environmental regulations.
PRESENTATION:
Vials containing 50 mL and 500 mL of net content.
Antibiotic with anti-inflammatory and analgesic action.
COMPOSITION:
Each mL of injectable solution contains:
Oxytetracycline base 200 mg
Diclofenac sodium 5 mg
Excipients q.s. to 1 mL
INDICATIONS:
Indicated in cattle for the treatment of respiratory diseases, foot infections, and hemoparasitic diseases (anaplasmosis) caused by Anaplasma marginale, Pasteurella multocida, Fusobacterium necrophorum, Staphylococcus spp., and Streptococcus spp.
Also indicated as an adjunct in the management of pain, fever, and inflammation associated with these conditions.
DOSAGE AND ROUTE OF ADMINISTRATION:
Deep intramuscular injection.
General dosage: 1 mL per 10 kg body weight, equivalent to 20 mg of oxytetracycline base/kg and 0.5 mg of diclofenac sodium/kg.
Do not administer more than 10 mL per injection site.
WITHDRAWAL PERIOD:
Animals must not be slaughtered for human consumption until 28 days after the end of treatment.
Milk produced during treatment and for 6 days after must not be used for human consumption.
CONTRAINDICATIONS:
Do not administer concomitantly with other non-steroidal anti-inflammatory drugs (NSAIDs) or glucocorticoids.
Due to the calcium-binding capacity of tetracyclines, avoid use in growing animals and pregnant females.
PRECAUTIONS:
Keep out of reach of children and domestic animals.
Store at temperatures not exceeding 30°C.
Veterinary prescription only.
Dispose of empty containers or residual contents according to current environmental regulations.
PRESENTATION:
Vials containing 50 mL and 500 mL of net content.
