Which statement is accurate regarding the Dietary Supplement Health and Education Act (DSHEA) of 1994? Select one: a. It mandates that herel product labels contain accurate information. b. It mandates that herbal product labels state that the products are not intended to diagnose, treat, cure, or prevent disease. c. It requires that herbal products undergo the same rigorous testing as drugs do under the FDA.

Which statement is accurate regarding the Dietary Supplement Health and Education Act (DSHEA) of 1994? Select one: a. It mandates that herel product labels contain accurate information. b. It mandates that herbal product labels state that the products are not intended to diagnose, treat, cure, or prevent disease. c. It requires that herbal products undergo the same rigorous testing as drugs do under the FDA.

Case Studies In Health Information Management

3rd Edition

ISBN:9781337676908

Author:SCHNERING

Publisher:SCHNERING

Chapter2: Information Protection: Access, Archival, Privacy, And Security

Section: Chapter Questions

Problem 2.1.1C

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The Food and Drug Administration (FDA) is responsible for: A. Requiring drug manufacturers to provide notice that a new drug is safe. B. Recalling pharmaceuticals only after harm has occurred. C. The approval before a new drug can be marketed. D. The assumption that the manufacturer of drugs would have conducted safety tests before marketing a new drug and protocols have been established.
During a home visit , Magdalena who is multigravida at 32 weeks ' gestation , tells the Nurse Marina that she craves and often eats laundry starch for lunch and usually has bowl of soup for supper Total weight gain to date has been 12 ( 5kg). A priority nursing diagnosis for the patent is: a. Altered parenting related to single status b.Noncompliance to insufficient resources c.Altered nutrition less than body requirements , related to pica d.Ineffective individual coping related to pregnancy
Have you ever encountered a situation in which you experienced (or had another person experience) a drug (OTC or prescription), herbal, or supplement-nutrient interaction? If so, explain what it was. If you have not, research a common interaction and explain it. Your explanation should include what drugs, herbs, or supplements and nutrient(s) are involved as well as the possible result of the interaction. Note that you are not to report on the side effects of a drug, herb or supplement, but rather how these might interact with a nutrient (in foods or in supplemental form) and result in a negative effect.
PBMs (select all that apply) A. manage patient drug benefits for health insurers, large employers, Medicare prescription drug plans, and other entities that provide health benefits. B. negotiate price discounts from drug manufacturers and determine how pharmacies get reimbursed for distributing prescriptions C. design formularies, lists of preferred drugs within a health plan D. determine the amount patients pay through copayments. E. Provide prescriptions for medications required
Manufacturers of self-contained test kits apply for and receive Food and Drug Administration (FDA) approval for their particular test to be on the Clinical Laboratory Improvement Amendment (CLIA) waived list. To find out if your particular brand of self-contained test kit is on the CLIA waived list, access an up-to-date listing at the FDA website(https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfclia/analyteswaived.cfm (Links to an external site.)) and use the key search term “Currently Waived Analytes” (be forewarned, though, that the list is very long) (Cited from Chap. 37). Research the link to the FDA to find your kit name on the list. Discuss the following questions: Why would it be important to have this kit listed here? Can a POL use kits that are not listed?
The Orphan Drug Act provides special patent protection and financial support from the state government for drugs designed to treat patients with diseases or conditions that effect 200,000 people or less. O True O False
I. Most food manufacturers develop and sell a complete line of products for a multitude of feeding indications, therapeutic indications, flavors and species. A. Factors that should be evaluated when selecting or reevaluating product lines from different manufacturers to be offered in a clinic: Explain them: 1. Online store (use, availability, benefits, etc.)2. Satisfaction guarantees
Which of the statements below is true about pharmaceutical or drug packaging? a.) FDA maintains tight control over regulations b.) cost is a major consideration when designing a package c.) advertising and communicating with the consumer is important for both prescription and OTC drugs. d.) shelf life is always shorter than for food so must choose material appropriately.
Describe what is the difference between over the counter medicine and prescription medicine.
Describe the FDA approval process for assessing the safety and efficacy of a newly developed drug. What are advantages and disadvantages of this process?
what is the difference between over the counter medicine and prescription medicine?
The acronym, USP, referenced on the Data Analysis page refers to the United States Pharmacopeia. Which of the following statements is not true about the USP? a) mission is to improve global health by issuing public standards and related programs to ensure the quality, safety, and benefits of medicines and foods b) generates chemical reference standards and official test methods for medicines and foods to ensure their quality and safety c) is responsible to provide the U.S. with a reliable, affordable, universal mail service d) is a non-profit scientific organization founded in 1820 in Washington D.C.