The minimum inhibitory concentration (MIC) and minimal bactericidal co
ncentrations (MBC) of florfenicol were determined for isolates of Past
eurella haemolytica and Pasteurella multocida obtained from animals wi
th bovine respiratory disease (BRD). The MICs and MBCs of florfenicol
against these important BRD pathogens were found to be remarkably simi
lar. In a study involving the pharmacokinetic disposition and distribu
tion of florfenicol, calves were given two doses of florfenicol (20 mg
/kg) intramuscularly 48 hours apart. Serum, bronchial secretion (BS) a
nd tissue cage fluid (TCF) concentrations were measured for 48 hours a
fter the initial dose and for 60 hour;following the second dose. Florf
enicol achieved excellent penetrations in both BS and TCF, and concent
rations in BS were higher than those in serum, showing the affinity of
florfenicol for lung tissue. Safety studies were performed in which c
attle were given the commercial formulation of florfenicol (NUFLOR(R)
Schering-Plough Animal Health(2)) at up to 10 times the recommended do
se via intramuscular injection. Some side effects were associated with
these higher dosages but were transient and reversible. NUFLOR(R) was
well tolerated by cattle following intramuscular administration. The
neck musculature was identified as the preferred site of administratio
n.