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10 years ago
A client who is considering taking a dietary supplement recommended by the nurse asks how to determine whether the supplement is safe. Which requirements by the Dietary Supplement and Nonprescription Drug Consumer Protection Act of 2007 will the nurse educate the client about?


1. Include their contact information on the label so consumers can report adverse effects.
2. Notify the Food and Drug Administration (FDA) within 15 days of receiving a report of an adverse effect.
3. Keep records of adverse effects for at least 6 years and make these records available for inspection by the Food and Drug Administration (FDA).
4. Demonstrate product effectiveness prior to release of the product to the public.
5. State which conditions the product is intended to cure or prevent.
Textbook 
Pharmacology: Connections to Nursing Practice

Pharmacology: Connections to Nursing Practice


Edition: 3rd
Authors:
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First-year pharmacology student, representing MIT!
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nginngin
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10 years ago
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BreakFree Author
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#2
10 years ago
Sounds and feels right, thank you for the rationale.
First-year pharmacology student, representing MIT!
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#3
10 years ago
No problemo! I knew you would appreciate the reasoning.
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