دراكسين
Draxxin (tulathromycin) Injectable Solution is a semi-synthetic macrolide antimicrobial containing 100 mg/mL of tulathromycin. Indicated for the treatment of bovine respiratory disease (BRD), infectious bovine keratoconjunctivitis (IBK/pinkeye), and bovine foot rot, as well as treatment and control of swine respiratory disease (SRD).
Dosage Form
N/A
Product Type
Pharmaceutical
Manufacturer
Package
50 mL, 100 mL, 250 mL, and 500 mL vials
| Species | Dosage | Route | Duration |
|---|---|---|---|
| Cattle | 2.5 mg/kg (1.1 mL/100 lb body weight) | Subcutaneous (SC) | Single injection |
| Swine | 2.5 mg/kg (0.25 mL/22 lb body weight) | Intramuscular (IM) | Single injection |
| Species | Meat (days) | Milk (days) | Eggs (days) |
|---|---|---|---|
| Cattle | 18 | ||
| Swine | 5 |
Treatment of bovine respiratory disease (BRD) associated with Mannheimia haemolytica, Pasteurella multocida, Histophilus somni, and Mycoplasma bovis.
Control of respiratory disease in cattle at high risk of developing BRD.
Treatment of infectious bovine keratoconjunctivitis (IBK) associated with Moraxella bovis.
Treatment of bovine foot rot (interdigital necrobacillosis) associated with Fusobacterium necrophorum and Porphyromonas levii.
Treatment of swine respiratory disease (SRD) associated with Actinobacillus pleuropneumoniae, Pasteurella multocida, Bordetella bronchiseptica, and Haemophilus parasuis.
Do not use in animals with known hypersensitivity to macrolide antibiotics.
Subcutaneous administration in cattle can cause transient tissue reaction at injection site.
Effects of tulathromycin on bovine or swine reproductive performance, pregnancy, and lactation have not been determined.
Transient local pain or swelling at the injection site.
Draxxin Prescribing Information
Leaflet100 mg/mL
Manufacturer
No alternatives available.