Flunixin meglumine is the only FDA-approved drug used in lactating dairy cattle for control of pyrexia associated with bovine respiratory disease and endotoxemia and for the control of relaxed inflammation.
In addition, Vazalore is the one FDA-approved human aspirin product that veterinarians may use in food-producing species under specific conditions, according to the Animal Medicinal Drug Use Clarification Act, also known as AMDUCA.
To allow extralabel drug use, a valid veterinarian-client-patient relationship must be established, an appropriate withdrawal time must be assigned, violative residues must not result, and only approved human or animal drugs may be used. AMDUCA says a veterinarian should not prescribe a drug in an extralabel manner if there is an approved drug that is labeled for the indication unless that labeled therapy is ineffective as determined by the veterinarian.
Because Vazalore is only available in 81 mg and 325 mg dosages, the FDA says veterinarians and dairy farmers may instead be using unapproved aspirin products, which come in larger dosages. Although other human aspirin products are marketed under an over-the-counter monograph, that monograph is not an approval and, therefore, these products cannot be used in an extralabel manner.
AABP leaders met with FDA’s Center for Veterinary Medicine for clarification on the extralabel use of aspirin.
“Previously, FDA has stated that aspirin use was of low regulatory concern; however, due to its increased use, questions from the public about its use, and the availability of labeled products for treatment of pyrexia (flunixin), they have shifted this stance to state such use is illegal,” according to an October 12 AABP announcement to its members.
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