FDA approves first pain meds for food-producing animals
WASHINGTON DC - The U.S. Food and Drug Administration has approved the first medication for pain control in a food-producing animal.
Banamine Transdermal (flunixin transdermal solution), is an animal drug approved for the control of pain associated with foot rot and the control of pyrexia (fever) associated with bovine respiratory disease.
Foot rot is a painful disease of the foot in which the skin in between the two toes becomes irritated, inflamed, and starts to decay. Affected cattle can become severely lame and the disease can affect deeper structures of the foot and leg if not treated.
Although other therapies are available for treating foot rot, there was no approved drug to control the pain associated with this disease until now.
Banamine Transdermal is also approved for the control of pyrexia (fever) associated with bovine respiratory disease in cattle. Bovine respiratory disease can be caused by bacterial, viral, fungal and/or parasitic pathogens.
Bovine respiratory disease affects the lower respiratory tract and lungs (pneumonia) or the upper respiratory tract (rhinitis, tracheitis, and bronchitis) and cattle typically present with fever.
The topical formulation of Banamine Transdermal provides a new way to administer flunixin to cattle. Banamine Transdermal is approved for a single application of a dose of 3.3 mg flunixin per kilogram body weight topically in a narrow strip along the back.
This non-steroidal anti-inflammatory medication is approved for use in steers, beef heifers, beef cows, beef bulls intended for slaughter and replacement dairy heifers under 20 months of age.
It is not for use in beef bulls intended for breeding; dairy bulls; female dairy cattle 20 months of age or older (including dry dairy cows); and suckling beef calves, dairy calves, and veal calves.
As this is a prescription medication, it can only be used by or on the order of a licensed veterinarian.
The application for Banamine Transdermal is sponsored by Intervet, Inc.