Is it safe to give zubrevo to calves?
Do not use in calves to be processed for veal. The effects of ZUPREVO ® 18% on bovine reproductive performance, pregnancy and lactation have not been determined. Swelling and inflammation, which may be severe, may be seen at the injection site after administration.
How is zuprevo used to treat bovine respiratory disease?
Treating bovine respiratory disease and controlling respiratory disease in cattle at high risk shouldn’t be difficult. Administering fast-acting, long-lasting ZUPREVO® (tildipirosin) is easy. Helps you get more doses per bottle.
How many doses of tildipirosin per bottle of zuprevo?
Administering fast-acting, long-lasting ZUPREVO® (tildipirosin) is easy. Helps you get more doses per bottle. Easy to calculate.
Is it safe to give zuprevo to humans?
ZUPREVO. The macrolide with a high margin of safety. As a new chemical entity, ZUPREVO antibiotic establishes a level of animal and consumer safety. Caution should be taken to avoid accidental self injection. In the case of human injection, seek medical advice immediately and show the package insert or label to the physician.
How long does zuprevo 18% stay in cattle?
Zuprevo 18%. For use in beef and non-lactating dairy cattle. Each ml of Zuprevo contains 180 mg tildipirosin. A single dose of Zuprevo concentrates in the lungs for 28 days and in bronchial fluid for 21 days to treat and control BRD. Administer one dose, 1 ml per 100 lbs. SQ in the neck, not to exceed 10 ml per injection site.
Do not use in calves to be processed for veal. The effects of ZUPREVO ® 18% on bovine reproductive performance, pregnancy and lactation have not been determined. Swelling and inflammation, which may be severe, may be seen at the injection site after administration.
How much tildipirosin is in zuprevo 18%?
Zuprevo™ 18% is a ready-to-use sterile injectable solution containing tildipirosin, a semi-synthetic macrolide antibiotic. Each mL of Zuprevo™ 18% contains 180 mg of tildipirosin as the free base, 82.5 mg citric acid monohydrate and 400 mg propylene glycol, and water qs with citric acid monohydrate added to adjust pH.
Are there any safety studies for zuprevo 18%?
SAFETY: A target animal safety study was conducted using Zuprevo™ 18% administered in 5-month-old cattle as three subcutaneous doses of 4, 12, or 20 mg/kg BW given 7 days apart (1X, 3X, and 5X the labeled dose). Animals remained clinically healthy during the study at the labeled dose.