Pharmacotherapeutics for Nurse Practitioner Prescribers 3rd Edition by Teri Moser Woo
Pharmacotherapeutics for Nurse Practitioner Prescribers 3rd Edition by Teri Moser Woo
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Chapter 4: Legal and Professional Issues in Prescribing
Complete Chapter Questions With Answers
Sample Questions Are Posted Below
Multiple Choice
Identify the choice that best completes the statement or answers the question.
____ 1. The U.S. Food and Drug Administration (FDA) regulates:
| A. | Prescribing of drugs by MDs and NPs |
| B. | The official labeling for all prescription and over-the-counter drugs |
| C. | Off-label recommendations for prescribing |
| D. | Pharmaceutical educational offerings |
____ 2. The U.S. Food and Drug Administration (FDA) approval is required for:
| A. | Medical devices, including artificial joints |
| B. | Over-the-counter vitamins |
| C. | Herbal products, such as St John’s Wort |
| D. | Dietary supplements, such as Ensure |
____ 3. An Investigational New Drug (IND) is filed with the FDA:
| A. | When the manufacturer has completed Phase III trials |
| B. | When a new drug is discovered |
| C. | Prior to animal testing of any new drug entity |
| D. | Prior to human testing of any new drug entity |
____ 4. Phase IV clinical trials in the United States are also known as:
| A. | Human bioavailability trials |
| B. | Post-marketing research |
| C. | Human safety and efficacy studies |
| D. | The last stage of animal trials before the human trials begin |
Answer Section
MULTIPLE CHOICE
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