Oxytetracycline and Flunixin meglumine injection
  • Oxytetracycline and Flunixin meglumine injection
  • Oxytetracycline and Flunixin meglumine injection
  • Oxytetracycline and Flunixin meglumine injection
  • Oxytetracycline and Flunixin meglumine injection

Oxytetracycline and Flunixin meglumine injection

For veterinary use only

COMPOSITION

Each ml contains Oxytetracycline 100mg and Flunixin meglumine 2mg.

INDICATIONS

For the control and treatment of infectious diseases of cattle caused by or associated with organisms sensitive to oxytetracycline, where concurrent analgesic, anti-inflammatory, anti-endotoxic or antipyretic therapy is desired. The product is especially indicated for the treatment of respiratory disease (particularly that associated with Mannheimia and Pasteurella infection) and acute mastitis (in conjunction with appropriate intramammary therapy).

DOSAGE AND ADMINISTRATION

For intramuscular injection.

Cattle: 1 ml/10 kg body weight daily for up to 5 days.

ADVERSE RACTION

Prolonged use of NSAIDs, including flunixin, may predispose or lead to gastrointestinal ulceration.

Reports of adverse reactions associated with oxytetracycline administration include injection site swelling, restlessness, ataxia, trembling, swelling of eyelids, ears, muzzle, anus and vulva (or scrotum and sheath in males), respiratory abnormalities (labored breathing), frothing at the mouth, collapse and possibly death. Some of these reactions may be attributed either to anaphylaxis (an allergic reaction) or to cardiovascular collapse of unknown cause. 

SPECIAL WARNINGS

Do not administer other NSAIDs concurrently or within 24 hours of each other.

Do not inject more than 20 ml intramuscularly at a single site. 

WITHDRAWAL PERIOD

Meat: 21 days.

Do not use in cattle producing milk for human consumption.

STORAGE

Seal and protect from light.

Keep out of reach of children.

PACKAGING

100ml/bottle

SHELF LIFE 

3 years.