DISPENSING VETERINARY PRESCRIPTION DRUGS: AN OVERVIEW Final Examination Questions Select the best answer for each question and mark your answers on page 84. For faster service, complete your test online at EliteLearning.com/Book
7. Which of the following statements is true about stocking compounded drugs in a practice’s pharmacy for use in that practice’s patients? a. Any compounded drug can be stored in your clinic for use within the context of a valid VCPR. b. Compounded drugs on the FDA’s List of Bulk Drug Substances for Compounding Office Stock Drugs for Use in Nonfood-Producing Animals can be stocked in a veterinary practice. c. No compounded drugs can be used in companion animals, regardless of the circumstances. d. Compounded drugs can only be prepared with an individual patient prescription. 8. Which of the following may be an appropriate scenario for the extra-label use of an animal drug? a. A groomer decides to administer a drug in an extra-label manner to a pet in his care. b. A human drug is added to cattle feed in an extra- label manner. c. Chloramphenicol is prescribed in an extra-label manner to treat a canine infection. d. A veterinarian prescribes an extra-label drug within the context of a VCPR. 9. Under what circumstances can a veterinarian prescribe extra-label drugs to a food animal patient within the context of a VCPR? a. There is no other available treatment option for a diagnosed disease that threatens the animal’s health. b. There is no available test to assess for the presence of drug residues in the animal’s tissue. c. The producer wants to increase weight gain and feed efficiency in his animals. d. The producer would like to add the drugs to his animals’ feed. 10. An FDA-approved animal drug is used in an approved manner, and an adverse drug reaction occurs. Who should the veterinarian contact? a. Drug manufacturer.
1. Which of the following agencies regulates topically- applied flea preventatives? a. Food and Drug Administration. b. Environmental Protection Agency. c. Center for Veterinary Biologics. d. Animal and Plant Health Inspection Service. 2. Which of the following agencies issues regulations that apply to canned pet foods? a. Food and Drug Administration. b. Environmental Protection Agency. c. Center for Veterinary Biologics. d. Animal and Plant Health Inspection Service. 3. Which of the following items would be subject to FDA regulation? a. A vaccine for canine parvovirus. b. A screening test kit for drug residues. c. A topical flea preventative. d. A non-therapeutic grooming aid for dogs. 4. In order for a drug to be approved for use in food animals, testing must be performed to ensure that drug residues are safe for human consumption. Who performs this testing? a. Food and Drug Administration. b. Center for Veterinary Biologics. c. Animal and Plant Health Inspection Service. d. The drug’s manufacturer.
5.
According to federal requirements, which of the following pieces of information must be included on a veterinary prescription drug label? a. Client address.
b. Veterinarian’s name. c. Drug manufacturer. d. Generic name of the medication. 6. Medicated animal feed regulations dictate which of the following characteristics of the feed? a. Uses and duration of therapy. b. Uses and potency levels. c. Duration of therapy and potency levels. d. Duration of therapy and client characteristics.
b. Food and Drug Administration. c. Center for Veterinary Biologics. d. Environmental Protection Agency.
Course Code: VFL01VP
EliteLearning.com/Veterinarian
Book Code: VFL1526
Page 6
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