The Veterinary Biologics Pharmacovigilance Program is for the ongoing surveillance of adverse events associated with animal vaccines and other immunobiologics, in cooperation with the veterinary profession and the veterinary immunobiologic industry.
A: An immunobiologic product (also known as a biological product) is one which modulates the immune system for the prevention, treatment, or diagnosis of disease. Veterinary biological products are used to prevent disease include vaccines or toxoids which stimulate an animal to produce antibodies against specific organisms or substances. This is termed active immunization. Passive immunization may be obtained from antibody-containing products such as serum derivatives; they may be used to treat disease. Immunobiological reactions are increasingly used as the basis of test kits for the diagnosis of disease.
A: The immunologically active ingredients in an immunobiologic may be either antigens or antibodies. Antigens are derived from killed or attenuated live disease organisms, such as viruses and bacteria. Antibodies may be derived from the blood or milk of donor animals who are often immunized against specific antigens. Other components of immunobiologics include the fluid suspension medium, preservatives or antibiotics, stabilizers, and adjuvants, which are substances which enhance the immune reaction. Licensed manufacturers of animal immunobiologics are regularly inspected to verify that production is done in accordance with approved procedures. Products intended for use in animals must be tested for purity, safety, and potency before they may be marketed. As a further check on the manufacturer's quality control, the USDA regularly tests randomly selected lots of all products in its own laboratory.
A: Postmarketing surveillance of veterinary immunobiologics has two main functions. One is to serve as an alert system for detecting the possibility that a product may not be performing as intended. An alert is triggered when information has been received which implicates a product as the cause of events which appear to be unusual in nature or frequency. The immediate response to an alert is an evaluation of the possibility the product is defective. The alert may be confirmed, rejected, or more information may be sought. Confirmation of an alert could trigger an intervention. Fortunately, this is a rare occurrence.
Postmarketing surveillance also provides an essential source of descriptive baseline information about the behavior of a vaccine or other immunobiologic when it is used under everyday field conditions. This type of information is a valuable reference in guiding our expectations and comparing situations which appear unusual. Temporal or geographical trends may become apparent.
A: An adverse event is any undesirable occurrence after the use of an immunobiological product, including illness or reaction, whether or not the event was caused by the product.
A: Some animals, like people, may be uncomfortable or lethargic the day they are vaccinated. More serious adverse events are a less common possibility. Immune (hypersensitivity) reactions are infrequent but possible after exposure to any immunobiologic, as well as many other substances. Acute anaphylaxis with immediate collapse is a dramatic reaction that may happen shortly after vaccination. It is important to observe an animal for at least an hour after vaccination, so that it may be treated if necessary. Other reactions that have been observed within a day of vaccination include loss of appetite, fever, facial swelling, hives, nasal or ocular discharge, respiratory distress, vomiting, or diarrhea. Events occurring a day to two weeks after vaccination include similar events, as well as stiffness, local inflammation, and systemic illness, which may or may not be based on an immune reaction. If you have any concerns about the health of an animal after the use of an immunobiologic, consult your veterinarian promptly.
Your veterinarian is also an important source of guidance about the proper administration of immunobiologics. Not all properly vaccinated animals will be immune to disease under all circumstances. Many factors affect the response of a particular animal to vaccination and the chance that it will subsequently succumb to disease. Such factors include the animal's immune competency, its health at the time of vaccination, stress, environment, and the virulence of the pathogen. Even under optimal conditions, antigens vary widely in the strength and duration of the disease protection they confer.
A: Good estimates of the rates of various types of adverse events after the use of veterinary immunobiologics are not readily available. The information we have is based on voluntary spontaneous reports to manufacturers and the USDA. While it may be possible to calculate a reporting rate, the relationship between a reporting rate and an incidence rate is not clear. This relationship may vary by type and severity of event, species, manufacturer, and even from one month to the next. Under appropriate conditions, a reporting rate may sometimes be used to estimate minimum incidence, which may be used for certain comparisons.
A: The mission of the USDA is to ensure that animal immunobiologics are in compliance with the Virus-Serum-Toxin Act. Reports are assessed for the possibility of a product deficiency. When necessary, testing is performed or additional information is sought. The USDA is, however, unable to make diagnoses or recommendations specific to individual cases. Some of the manufacturers do provide such services. Receipt of a report by the USDA does not necessarily imply that the product caused an adverse event, or even that a particular event actually occurred.
A: Veterinary immunobiologics are regulated by the United States Department of Agriculture, Center for Veterinary Biologics (USDA, CVB) under the Virus-Serum-Toxin Act. The CVB maintains pharmacovigilance. An adverse event report enters this program through several channels.
Adverse events may be reported to the:
Manufacturer. Many biologics manufacturers maintain veterinary services departments to handle such reports and may also offer diagnostic advice, treatment recommendations, and guidance on product use.
Center for Veterinary Biologics (CVB). Once an adverse event has been reported to the manufacturer, the CVB may be contacted by submission of the electronic Adverse Event Report worksheet. This worksheet may be downloaded and submitted by FAX to (515) 337-6120 or by mail to the CVB. Adverse events may also be reported by calling the CVB at (800) 752-6255, if necessary.
Veterinary drugs, medicated feeds, and animals devices are regulated by the Food and Drug Administration, Center for Veterinary Medicine (FDA, CVM) under the Food, Drug and Cosmetic Act. The CVM recommends that you first contact the manufacturers to report an adverse event. To contact the CVM directly, call (888) FDA-VETS.
Topical insecticides. Most of the products used topically for the control of ectoparasites and insects on animals are regulated by the Environmental Protection Agency (EPA) under the Federal Insecticide Fungicide and Rodenticide Act. The EPA may be reached at (800) 858-7378.
A: In the event of a serious human exposure to a veterinary immunobiologic, such as inadvertently injecting oneself with a vaccine intended for animals, contact your physician or emergency room at once. Be prepared to inform your physician about the product to which you were exposed. Your physician may wish to contact the manufacturer for additional information about the product. The CVB may be able to facilitate the communication of important information, if necessary.