Why should dietary supplements be viewed differently than prescriptive medications? 1. Supplement manufacturers must determine potential risk of their products and voluntarily remove them from the consumer market. 2. Supplements are tested and marketed to ensure safety whereas prescriptive medications are not tested. 3. Medications undergo required review by the Food and Drug administration whereas dietary supplements do not. 4. Dietary supplements contain only natural ingredients whereas prescriptive medications contain synthetic compounds.

Based on the device classification provide a few sentences for device-specific FDA requirements, and regulations.

To get approved by the FDA generic drugs have to demonstrate the following: That their bio availability is the same as brand name drug That their bio equivalence is the same as the brand name drug That their bio availability AND bio equivalence is the same as the brand name drug None of the above

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Clinical trials can be designed to demonstrate that a new technology offers measurable, relevant benefits, in terms of safety, clinical effectiveness, and in some instances, cost-effectiveness True False

5. Claims for any medical device do not need to be supported by data for commercialization. A. True B. False 6. For a drug-device combination product approval, the FDA allows device testing using a placebo instead of an actual drug if the drug is costly. A. True B. False 7. Sharing product information on Twitter without data support is acceptable since Twitter is a social media, not an actual rug packaging. A. True В. False Page 5 of bedo e o

cription 1. List the most dangerous drugs you believe that affect American life. Describe what we can do to intervene people to use those deadly drugs (hint: can discuss from individual, family, community and nationwide).

1. Which of the following makes it especially difficult for veterinarians to determine if an opioid is truly indicated? A. Opioids used in veterinary medicine are not used in human medicine B. Our patients can’t talk C. Our patients always require larger doses than humans D. All of the above   2. Which of the following is/are potential problems with PDMPs in veterinary medicine? A. Determining how to report the data B. Potential HIPPA violations when reviewing the system seeing the client’s medical information C. How to tie pets to the people that we are trying to monitor D. All of the above   3. Which schedule of controlled substance has no accepted medical use? A. CI B. CII C. CIII D. CIV   4. Which state specific regulatory agencies do you need to be familiar with to know how they regulate controlled substances at the state level? A. Local DEA Field Office B. State Board of Pharmacy C. State Veterinary Board D. All of the…

Education is a critical elements of Standard Precautions but training is not required   Question options: A) True B) False

Which of the following is FALSE about provisions of the Dietary Supplement Health and Education Act (DSHEA)? O a. Dietary ingredients in supplements must be federally regulated and generally recognized as safe (GRAS) O b. Dietary supplements must be properly and truthfully labeled O c. DSHEA provided a definition of dietary supplement O d. The FDA is responsible for ensuring that a supplement is safe, unadulterated, and check that it has been produced with good manufacturing practices