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

Author Question: What was the rationale for the 1992 changes in the Food and Drug Administration's regulations to ... (Read 27 times)

Wadzanai

  • Hero Member
  • *****
  • Posts: 528
What was the rationale for the 1992 changes in the Food and Drug Administration's regulations to permit accelerated approval of drugs for the treatment of life-threatening or severely debilitating disease?
 
  a. To allow for marketing before completion of phase II of drug trials
  b. To ensure that the unknown risks associated with early approval are balanced by the need for effective drugs
  c. To change the rules because existing FDA regulations were too stringent for potentially effective drugs
  d. To accelerate approval of new drugs to give prescribers the option of using them without research findings

Question 2

A nurse is providing education to a patient preparing for discharge from the clinic. The nurse understands that the best way to promote compliance in the patient going home on a new medication is to
 
  a. provide a video for the patient to watch at home.
  b. provide a pamphlet on the new medication.
  c. monitor the patient for an adverse drug response prior to discharge.
  d. ask the patient to restate the instructions and verify understanding.



Related Topics

Need homework help now?

Ask unlimited questions for free

Ask a Question
Marked as best answer by a Subject Expert

fffftttt

  • Sr. Member
  • ****
  • Posts: 322
Answer to Question 1

ANS: B
Accelerated drug approval was needed to ensure that effective drugs necessary for life-threatening and/or severely debilitating diseases were available but with a balance of benefit/effectiveness and risk.
Phase II drug trials are related to the therapeutic utility and dosage range, not to accelerated approval of drugs.
FDA regulations were not stringent enough, but became so over time to protect consumers.
Accelerated approval of new drugs did not give prescribers the option to use them without research findings. Drugs are approved only after a rigorous clinical trial and research process.

Answer to Question 2

ANS: D
Having the patient to restate the instructions allows the nurse to verify patient understanding.
The nurse will not be able to assess whether the patient learned from the video, because the patient will watch it at home after discharge.
The nurse will not be able to assess whether the patient actually read the pamphlet and understood its contents.
Monitoring the patient does not ensure compliance with the medication and is not indicated in this situation.





 

Did you know?

The human body's pharmacokinetics are quite varied. Our hair holds onto drugs longer than our urine, blood, or saliva. For example, alcohol can be detected in the hair for up to 90 days after it was consumed. The same is true for marijuana, cocaine, ecstasy, heroin, methamphetamine, and nicotine.

Did you know?

The most destructive flu epidemic of all times in recorded history occurred in 1918, with approximately 20 million deaths worldwide.

Did you know?

People who have myopia, or nearsightedness, are not able to see objects at a distance but only up close. It occurs when the cornea is either curved too steeply, the eye is too long, or both. This condition is progressive and worsens with time. More than 100 million people in the United States are nearsighted, but only 20% of those are born with the condition. Diet, eye exercise, drug therapy, and corrective lenses can all help manage nearsightedness.

Did you know?

The term pharmacology is derived from the Greek words pharmakon("claim, medicine, poison, or remedy") and logos ("study").

Did you know?

After 5 years of being diagnosed with rheumatoid arthritis, one every three patients will no longer be able to work.

For a complete list of videos, visit our video library