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HomeInjectable FLUNIXAMINE
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FLUNIXAMINE

$60.00 $55.00

FLUNIXAMINE

BEEF: For control of fever caused by BRD

  • FLUNIXAMINE® (flunixin meglumine) Injectable Solution is indicated for the control of pyrexia associated with bovine respiratory disease (BRD).

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Description

FLUNIXAMINE

BEEF: For control of fever caused by BRD

  • FLUNIXAMINE® (flunixin meglumine) Injectable Solution is indicated for the control of pyrexia associated with bovine respiratory disease (BRD).

DAIRY: For control of pyrexia due to mastitis

  • FLUNIXAMINE is indicated for the control of pyrexia associated with endotoxemia and acute bovine mastitis. It also is indicated for the control of inflammation in endotoxemia.

HORSES: For pain relief

  • FLUNIXAMINE is recommended for the alleviation of inflammation and pain associated with musculoskeletal disorders. It also is recommended for the alleviation of visceral pain associated with colic.
  • Dosing & Administration

    Horse: The recommended dose for musculoskeletal disorders is 0.5 mg per pound (1 mL/100 lbs.) of body weight once daily. Treatment may be given by intravenous or intramuscular injection and repeated for up to 5 days. Studies show onset of activity is within 2 hours. Peak response occurs between 12 and 16 hours and duration of activity is 24 to 36 hours.

    The recommended dose for the alleviation of pain associated with equine colic is 0.5 mg per pound of body weight. Intravenous administration is recommended for prompt relief. Clinical studies show pain is alleviated in less than 15 minutes in many cases. Treatment may be repeated when signs of colic recur. During clinical studies approximately 10% of the horses required one or two additional treatments. The cause of colic should be determined and treated with concomitant therapy.

    Cattle: The recommended dose for control of pyrexia associated with bovine respiratory disease and endotoxemia and control of inflammation in endotoxemia is 1.1 to 2.2 mg/kg (0.5 to 1.0 mg/lb.; 1 to 2 mL per 100 lbs.) of body weight given by slow intravenous administration either once a day as a single dose or divided into two doses administered at 12-hour intervals for up to 3 days. The total daily dose should not exceed 2.2 mg/kg (1.0 mg/lb.) of body weight. Avoid rapid intravenous administration of the drug.

    The recommended dose for acute bovine mastitis is 2.2 mg/kg (1 mg/lb.; 2 mL per 100 lbs.) of body weight given once by intravenous administration.

    IMPORTANT SAFETY INFORMATION: FLUNIXAMINE has a four day pre-slaughter withdrawal time. Milk that has been taken during treatment and for 36 hours after the last treatment must not be used for food.  Not for use in dry dairy cows. Do not use in calves to be processed for veal. Do not use in bulls intended for breeding. NSAIDS are known to have potential effects on both parturition and estrus cycle. Intramuscular administration has resulted in illegal residues. Do not use in horses intended for food.

    Cattle
    IMPORTANT SAFETY INFORMATION:
     FLUNIXAMINE has a four day pre-slaughter withdrawal time. Milk that has been taken during treatment and for 36 hours after the last treatment must not be used for food.  Not for use in dry dairy cows. Do not use in calves to be processed for veal. Do not use in bulls intended for breeding. NSAIDS are known to have potential effects on both parturition and estrus cycle. Intramuscular administration has resulted in illegal residues.

    Equine
    IMPORTANT SAFETY INFORMATION:
     Do not use FLUNIXAMINE in horses intended for food. NSAIDS are known to have potential effects on both parturition and estrus cycle. Drug compatibility should be monitored closely in patients requiring adjunctive therapy.

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A180 100ML

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In cattle: Treatment of bovine respiratory disease caused by Mannheimia haemolytica, Pasteurella multocida and Histophilus somni sensitive to danofloxacin. For the treatment of acute bovine mastitis caused by Escherichia coli sensitive to danofloxacin. In neo-natal calves: Treatment of enteric infections caused by Escherichia coli sensitive to danofloxacin
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DUPHALYTER Electrolyte, Energy substance, Amino Acid and Vitamin in solution for injection Laboratorio PFIZER, SA. Pharmaceutical form: Solution for injection (Sol.i.) Composition per ml: Calcium chloride (dihydrate) 0.23 mg; magnesium sulfate (heptahydrate) 0.29 mg; potassium chloride 0.20 mg .; dextrose 45.46 mg; arginine (hydrochloride) 25 ƒÊg; cysteine ​​(hydrochloride monohydrate) 0.01 mg; Phenylalanine 0.03 mg; glutamic acid (sodium salt monohydrate) 0.04 mg; histidine (hydrochloride monohydrate) 0.01 mg;isoleucine 0.01 mg; leucine 0.04 mg; lysine (hydrochloride) 0.03 mg; methionine 0.01 mg; threonine 0.02 mg; tryptophan 0.01 mg; valine 0.05 mg; cyanocobalamin 0.05 ƒÊg; dexpanthenol 0.05 mg; nicotinamide 1.50 mg; pyridoxine hydrochloride 0.10 mg;riboflavin 0.04 mg; thiamine 0.10 mg. Pharmacological properties General characteristics: The product provides a correct balance between water, minerals, vitamins and amino acids, in those animals lacking any of these compounds. Interactions and incompatibilities: None known. Indications and target species: Birds: Dehydration and convalescence. Pigs, Bovine and Equine: Dehydration, anorexia, bacterial enteritis and convalescence. Dogs and Cats: Dehydration, anorexia, bacterial enteritis, vomiting and convalescence. Product, in general, also recommended as support therapy in animals weakened by electrolyte imbalance and hypoproteinemia; in cases of incompetence, surgical operations, hemorrhages, excessive sweating, vascular shocks, exhaustion, weight loss, fever, inflammation of the digestive tract, and before transport, in all pets. Contraindications: None known. Side effects: Intravenous administration too quickly can cause nausea, vomiting and general malaise. If this happened, it would be enough to interrupt the application until the animal returned to its normal state and then continue the administration at a lower speed. Intravenous administration route slow, intraperitoneal or subcutaneous. – Slow intravenous: pigs, cattle, horses, dogs and cats. – Intraperitoneal: pigs and cattle. – Subcutaneous: birds (at the back of the neck), pigs, cattle, dogs and cats. It is recommended to use sterile syringes and inject the preparation at body temperature. Dosage: Poultry: 10 ml / kg pv In 1-day-old chicks: 0.5 ml / chick. Pigs, Cattle and Equine: Adult animal: 20 ml / 10 kg pv Young animal: 60 ml / 10 kg pv Dogs and Cats: 10 ml / kg pv Administration may be repeated as many times as necessary. Waiting time: Not accurate. Conservation mode Store in a cool, dry place and protected from light. Observations: With veterinary prescription. Presentation Bottles with 500 ml.
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AMIGLYDE-V AMIKACIN SULFATE INJECTION FOR HORSES

Federal law restricts this drug to use by or on the order of a licensed veterinarian.
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