This topic contains a solution. Click here to go to the answer

Author Question: Nursing students are studying which drug types must have Food and Drug Administration (FDA) approval ... (Read 124 times)

SGallaher96

  • Hero Member
  • *****
  • Posts: 509
Nursing students are studying which drug types must have Food and Drug Administration (FDA) approval before being marketed. The students know that which drugs must have approval from the FDA before being marketed?
 
  1. Biologics
  2. Food supplements
  3. Herbal preparations
  4. Dietary supplements

Question 2

A pharmaceutical representative comes to the primary care office and states that his company is marketing a new drug that does not need approval by the Food and Drug Administration (FDA). What is the best response of the nurse?
 
  nurse?
  1. Is this a drug in clinical trials? Those are the only drugs that don't have to have FDA approval.
  2. Is this an over-the-counter drug? Over-the-counter drugs do not need FDA approval.
  3. Your company must be involved in academic research if the drug doesn't need FDA approval.
  4. Any pharmaceutical company must have FDA approval before marketing a drug.



Related Topics

Need homework help now?

Ask unlimited questions for free

Ask a Question
Marked as best answer by a Subject Expert

kilada

  • Sr. Member
  • ****
  • Posts: 311
Answer to Question 1

Correct Answer: 1
Rationale 1: Biologics must have FDA approval before being marketed.
Rationale 2: Food supplements do not require FDA approval.
Rationale 3: Herbal preparations do not require FDA approval.
Rationale 4: Dietary supplements do not require FDA approval.
Global Rationale: Biologics must have FDA approval before being marketed. Food supplements, herbal preparations, and dietary supplements do not require FDA approval prior to being marketed.

Answer to Question 2

Correct Answer: 4
Rationale 1: Drugs in clinical trials must have FDA approval to start and continue clinical trials.
Rationale 2: Over-the-counter drugs must have FDA approval before being marketed.
Rationale 3: Drugs involved in academic research must have FDA approval.
Rationale 4: All drugs marketed by pharmaceutical companies must have FDA approval.
Global Rationale: All drugs marketed by pharmaceutical companies must have FDA approval. Drugs in clinical trials must have FDA approval to start and continue clinical trials. Over-the-counter drugs must have FDA approval before being marketed. Drugs involved in academic research must have FDA approval.





 

Did you know?

Side effects from substance abuse include nausea, dehydration, reduced productivitiy, and dependence. Though these effects usually worsen over time, the constant need for the substance often overcomes rational thinking.

Did you know?

As of mid-2016, 18.2 million people were receiving advanced retroviral therapy (ART) worldwide. This represents between 43–50% of the 34–39.8 million people living with HIV.

Did you know?

Women are two-thirds more likely than men to develop irritable bowel syndrome. This may be attributable to hormonal changes related to their menstrual cycles.

Did you know?

Amphetamine poisoning can cause intravascular coagulation, circulatory collapse, rhabdomyolysis, ischemic colitis, acute psychosis, hyperthermia, respiratory distress syndrome, and pericarditis.

Did you know?

Vaccines prevent between 2.5 and 4 million deaths every year.

For a complete list of videos, visit our video library