The U.S. Food and Drug Administration (FDA) has approved Pulmotil, an innovative Bovine Respiratory Disease (BRD) treatment for groups of cattle in the early stages of a BRD outbreak that provides 14 days of sustained in-feed therapy, a practice that reduces stress associated with cattle handling.
Pulmotil is approved for the control of BRD associated with Mannheimia haemolytica, Pasteurella multocida and Histophilus somni in groups of beef and non-lactating dairy cattle, where active BRD has been diagnosed in at least 10 percent of the animals in the group.
“This approval brings cattle veterinarians and producers a truly new management tool for controlling BRD,” said Jeff Simmons, president, Elanco. “With the introduction of Pulmotil, Elanco continues to bring the beef and dairy industries highly effective treatment solutions that provide more BRD management flexibility.”
BRD is the most common disease among feedlot cattle, accounting for approximately 75% of feedlot morbidity and 50 percent to 70% of feedlot deaths,costing the industry an estimated $800 to $900 million annually in economic losses due to reduced feed efficiency, treatment costs and deaths.… Continue reading Read More »