New Antibiotic Restrictions Just Around the Corner
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The Food and Drug Administration’s (FDA) guidance to the industry takes effect in June of 2023, but what does that mean for livestock producers?
There are products that we use in veterinary medicine that we also use in human medicine. These products are often referred to as “medically important antimicrobials”. In 2017 the FDA began implementing the Guidance for the Industry #213 otherwise known as the Veterinary Feed Directive (VFD). Implementation of the VFD focused on veterinary oversight of medically important antimicrobials delivered to livestock via feed and/or water. The focus of FDA guidance 263 will primarily address the injectable and oral versions of these products such as penicillin, tetracycline and sulfa products. Guidance #263 recommends sponsors of medically important antimicrobial drugs that continue to be available over-the-counter (OTC) and approved for use in animals (companion and food producing), regardless of delivery mechanism, to voluntarily bring these products under veterinary oversight or prescription marketing status. These product labels will now contain the prescription (Rx) statement, "Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian."
While very little information about Guidance #263 was aimed towards livestock producers, this may have significant impacts on the way in which livestock owners are able to access antibiotic therapy for their animals. While this change does not require the purchase of products from a veterinarian, going forward, producers will be legally required to obtain a prescription from a licensed veterinarian with which the producer has a valid veterinary-client-patient relationship (VCPR). What this means for many producers is that products that they may have purchased from the local feedstore, farm supply, or local co-op may no longer be on those store shelves.
Much like when the veterinary feed directive was put in place in 2017, some of these businesses may simply pull these products from store shelves and decline to offer products as they do not have the framework in place to meet the legal burden of acting as a “Pharmacy” which requires the ability to review veterinary authorized prescriptions and track refills of those prescription products. For those that do continue to stock these products on their shelves, producers will have to produce a prescription prior to purchasing.
Those producers who already have a VCPR in place and purchase their animal health products through their veterinary office, or who purchase through other distributors under an existing prescription system, will likely notice little change in their ability to source these products. However, those producers that don’t consult a veterinarian on a regular basis will need to establish a valid VCPR prior to purchasing these products as they start to disappear from OTC access.
While the definition of a valid VCPR does vary from state to state, Nebraska’s definition of a valid VCPR is outlined in the Nebraska Veterinary Medicine and Surgery Practice Act as follows:
Veterinarian-client-patient relationship means that:
(1) The veterinarian has assumed the responsibility for making clinical judgments regarding the health of the animal and the need for medical treatment, and the client has agreed to follow the veterinarian's instructions;
(2) The veterinarian has sufficient knowledge of the animal to initiate at least a general or preliminary diagnosis of the medical condition of the animal. This means that the veterinarian has recently seen and is personally acquainted with the keeping and care of the animal by virtue of an examination of the animal or by medically appropriate and timely visits to the premises where the animal is kept; and
(3) The veterinarian is readily available or has arranged for emergency coverage and for follow-up evaluation in the event of adverse reactions or the failure of the treatment regimen.
Furthermore, Nebraska Beef Quality Assurance (BQA) recommends that you have a written documented VCPR form filled out with your herd veterinarian and that you get a copy of all documented prescriptions. These records should be maintained for at minimum 2 years. Nebraska BQA offers a VCPR form on their website under the resources tab that producers can print off and fill out with their veterinarian. This VCPR form should be updated or reviewed annually.
So, to the nitty gritty, what products should producers expect to see these changes for, and when will this happen?
The following are some products that will be seeing label changes to prescription-only status:
- Injectables: Liquamycin LA-200, Noromycin 300 LA, Bio-Mycin 200, Agrimycin 200, etc.
- Boluses: Terramycin Scours Tablets, OXY 500 Calf Boluses
- Penicillins (Penicillin G procaine, penicillin G benzathine)
- Injectables: Penicillin Injectable, Dura-Pen, Pro-Pen-G, Combi-Pen 48, etc.
- Intramammary tubes: Masti-Clear, Go-dry, Albadry Plus
- Sulfa-based antibiotics (Sulfadimethoxine, sulfamethazine)
- Injectables: Di-Methox 40%, SulfMed 40%
- Boluses: Albon, Sustain III Cattle & Calf Boluses, Supra Sulfa III Cattle & Calf Boluses
- Injectables: Tylan 50, Tylan 200
- Cephapirin, cephapirin benzathine
- Intramammary tubes: ToDAY and ToMORROW
Additionally, several swine medications fall under the new guidance:
- Injectables: Lincomix 100, Lincomix 300, LincoMed 100, LincoMed 300
- Injectables: Garasol, Gentamicin Piglet Injection
When Guidance #263 was published on June 11, 2021, it was structured with a two-year phase-in for manufacturers of these products to make label changes and come into compliance with the guidance so that they would be able to continue marketing their products without interruption. All products covered under Guidance #263 are to be removed from OTC availability by June 11, 2023. The expectation is that producers will see familiar products start to disappear from store shelves as OTC products over the next few months as manufacturers finalize label changes and refine their marketing and distribution channels to assure compliance with prescription requirements.
It is important to remember that these critical products are not being removed from the marketplace, but instead being brought under veterinary oversight in order to combat overuse/misuse due to OTC access. Furthermore, producers SHOULD NOT “stock-up” on these products to avoid needing a prescription once this change takes effect. Again, these products will STILL be readily available. Animal health products have expiration dates and are sensitive to storage time and conditions. Purchasing large quantities of animal health products may lead producers to have an excess of products unused by the date of the product’s expiration. Products used after the expiration date are less effective and may not work as intended and may lead to higher incidences of treatment failure. Disposal of expired antimicrobials can present challenges as well. In the long run, it is easier and safer to purchase products only when needed under the guidance of a veterinarian. Additionally, this guidance affects only medically important antibiotic products. Antiparasiticides, injectable and oral nutritional supplements, oral pro/prebiotics and topical non-antibiotic treatments will not be affected and will remain available through OTC marketing channels just as before. Now, more than ever, producers need to seek out and establish a VCPR with a trusted veterinarian to provide input on antibiotic selection for their operations so that the best treatment options can be selected with antibiotic stewardship, animal welfare, and livestock economics all important decision-making factors.
For more information:
CVM GFI #263 Recommendations for Sponsors of Medically Important Antimicrobial Drugs Approved for Use in Animals to Voluntarily Bring Under Veterinary Oversight All Products That Continue to be Available Over-the-Counter June 2021
FDA Finalizes Guidance to Bring Remaining Approved Over-The-Counter Medically Important Antimicrobial Drugs Used for Animals Under Veterinary Oversight
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