Draxxin 500 ML

$850.00

Draxxin Injectable Solution Is a Ready-to-use Sterile Parenteral Preparation Containing Tulathromycin, a Semi-synthetic Macrolide Antibiotic of the Subclass Triamilide. Each Ml of Draxxin Injectable Solution Contains 100 mg of Tulathromycin as the Free Base in a Propylene Glycol Vehicle.

Draxxin 500 ML

Beef and Non-lactating Dairy Cattle:
Bovine respiratory disease (BRD):For the treatment of BRD associated with Mannheimia haemolytica, Pasteurella multocida, Histophilus somni (Haemophilus somnus) and Mycoplasma bovis and for the reduction of morbidity associated with BRD in feedlot calves caused by Mannheimia haemolytica, Pasteurella multocida, Histophilus somni and Mycoplasma bovis, during the first 14 days in the feedlot when administered at the time of arrival.

Infectious bovine keratoconjunctivitis (IBK):For the treatment of IBK associated with Moraxella bovis.
Foot Rot:For the treatment of bovine foot rot (interdigital necrobacillosis) associated with Fusobacterium necrophorum and Porphyromonas levii.

Suckling Calves, Dairy Calves, and Veal Calves:
BRD:For the treatment of BRD associated with M. haemolytica, P. multocida, H. somni, and M. bovis.

Swine:
Swine respiratory disease (SRD):For the treatment of SRD associated with Actinobacillus pleuropneumoniae, Pasteurella multocida and Mycoplasma hyopneumoniae and for the control of SRD caused by Actinobacillus pleuropneumoniae, Pasteurella multocida and Mycoplasma hyopneumoniae in groups of pigs where SRD has been diagnosed.

Draxxin 500 ML Dosage & Administration

Cattle:
Inject subcutaneously in the neck, a single dose of 2.5 mg/kg body weight (1.25 mL/50 kg). Care should be taken to dose accurately. Do not inject more than 10 mL per injection site. Most animals will respond to treatment within 3 to 5 days. If no improvement is observed, the diagnosis should be re-evaluated.

On Arrival Treatment:
Note: To limit the development of antimicrobial resistance, Draxxin Injectable Solution should only be used as an arrival treatment when: 1) BRD has been diagnosed and 2) calves are at “high risk” of developing BRD. One or more of the following factors typically characterizes calves at “high risk” of developing BRD. Cattle are from multiple farm origins, and/or cattle have extended transport times (that may have included few if any rest stops), and/or ambient temperature change(s) from origin to arrival of 17°C or more, and/or animals have had continued exposure to extremely wet and cold weather conditions, and/or cattle have experienced excessive shrink or stressful processing procedures such as castration and dehorning.

Swine:
With the use of an automatic dosing syringe, inject intramuscularly in the neck, a single dose of 2.5 mg/kg body weight (0.25 mL/10 kg). Do not inject more than 2.5 mL per injection site. Most animals will respond to treatment within 3 to 5 days. If no improvement is observed, the diagnosis should be re-evaluated.

Note:
To limit the development of antimicrobial resistance, Draxxin Injectable Solution should only be used for control of SRD when segregation and treatment of individual sick animals is unlikely to control the disease outbreak. Veterinarians should make treatment decision by considering among others overall farm management and outbreak associated factors.

Contraindications & Warnings

CONTRAINDICATIONS:

Draxxin Injectable Solution is contraindicated in animals previously found to be hypersensitive to macrolide antibiotics.

WARNINGS:

Treated animals must not be slaughtered for use as food for at least 44 days in cattle and 8 days in swine, after the latest treatment with this drug. Do not use in dairy cows 20 months of age and older. To limit the development of antimicrobial resistance, Draxxin Injectable Solution should only be used (1) as an arrival treatment in feedlot calves when BRD has been diagnosed and calves are at high risk of developing BRD, and (2) for control of SRD outbreak when groups of pigs are at high risk of developing SRD. Keep out of reach of children.

Note:

To reduce the possibility of excess trim at the injection site it is recommended that swine not be slaughtered for up to 35 days after the latest treatment with this drug.

CAUTIONS:

The effects of Draxxin Injectable Solution on bovine and porcine reproductive performance, pregnancy and lactation have not been determined. Subcutaneous injection in cattle and intramuscular injection in swine can cause a local tissue reaction that may result in trim loss of edible tissue at slaughter. The safety of Draxxin Injectable Solution has not been demonstrated in pigs less than 4 weeks of age.  dexaphenyl 100ml

Pharmaceutical Precautions

Store between 15 and 30°C. Contents should be used within 28 days after the first dose is removed

Further Information

Presentation:
Draxxin Injectable Solution is available in 20 mL, 50 mL, 100 mL, 250 mL and 500 mL vials.

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