Arma
SEFANEL Enjeksiyonluk Çözelti Tozu ve Çözücüsü
VETERINARY SYSTEMIC ANTIBACTERIAL - INJECTABLE
Description
CONTENT:
Each powder vial contains 1 g ceftiofur (as ceftiofur sodium) Ceftiofur
and each solvent vial contains 20 ml solvent. Each ml of
reconstituted solution contains 50 mg ceftiofur (as ceftiofur 50mg
sodium).
INDICATIONS:
Bacteria sensitive to ceftiofur in Cattle;
For the treatment of bacterial respiratory disease associated with Mannheimia haemolytica (former
Pasteurella haemolytica), Pasteurella multocida and Histophilus somni (former Haemophilus
somnus). For the treatment of acute interdigital necrobacillosis (panaritium, foot rot), associated
with Fusobacterium necrophorum and Bacteroides melaninogenicus (Porphyromonas
asaccharolytica).
Bacteria sensitive to ceftiofur in Horses;
For the treatment of horses with bacterial respiratory disease associated with Streptococcus
zooepidemicus, Streptococcus equi, Staphylococcus spp. and/or Pasteurella spp.
USAGE AND DOSAGE:.
This product is for intramuscular use only. Inject the exact volume of solvent into sterile powder
vial. Shake solution until complete reconstitution of powder occurs. For cattle: Respiratory disease:
1 mg/kg body weight/day (1 ml product/50 kg body weight/day) for 3 to 5 days Acute interdigital
necrobacillosis: 1 mg/kg body weight/day (1 ml product/50 kg body weight/day) for 3 days. For
horse: Respiratory disease: 2 mg/kg body weight/day (2 ml product/50 kg bodyweight/day) for 10
days (or up to 48 hours after clinical signs have disappeared). If no response is seen within 4-5
days, the diagnosis should be re-determined.
DRUG RESIDUE CAUTIONS:
Cattle should not be slaughtered for human consumption
during treatment and within 2 days of the last treatment. “0”
days for milk in cattle.
PRESENTATION: It is presented in vials of 50 ml, 100 ml and
250 ml.
TARGET SPECIES: Cattle,Horse
WITHDRAWAL PERIOD
Cattle: 2 days
Milk: “0” days
SHELF LIFE : 24 MONTHS