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

Author Question: Which laboratory test best evaluates HIV disease? 1. Platelets 2. Liver function studies 3. CD4 ... (Read 84 times)

nevelica

  • Hero Member
  • *****
  • Posts: 563
Which laboratory test best evaluates HIV disease?
 
  1. Platelets
  2. Liver function studies
  3. CD4 count
  4. Complete blood count

Question 2

A client expresses concerns about a newly prescribed medication. The nurse explains that the safety and effectiveness of the medication have been proven, according to the statutes of which law?
 
  1. Public Health Service Act
  2. FDA Modernization Act
  3. Food, Drug, and Cosmetic Act
  4. Pure Food and Drug Act



Related Topics

Need homework help now?

Ask unlimited questions for free

Ask a Question
Marked as best answer by a Subject Expert

yasmina

  • Sr. Member
  • ****
  • Posts: 323
Answer to Question 1

3
Rationale 1: Platelets levels do not evaluate HIV disease.
Rationale 2: Liver function studies can be used but do not assess the progress.
Rationale 3: CD4 count best determines the progress of the disease.
Rationale 4: Complete blood count can be used but does not assess the progress.
Global Rationale: CD4 count best determines the progress of the disease. Platelets do not evaluate HIV disease. Liver function studies and complete blood counts can be useful in treatment but do not assess the progress.

Answer to Question 2

3

Rationale 1: The Public Health Service Act of 1944 covers many health issues, including biological products and the control of communicable diseases.
Rationale 2: The FDA Modernization Act is the largest reform effort of the drug review process since 1938.
Rationale 3: The Food, Drug, and Cosmetic Act, passed in 1938, prevents the marketing of drugs that have not been thoroughly tested prior to marketing. Drug companies are required to prove the safety and efficacy of any drug before it can be sold in the United States.
Rationale 4: The Pure Food and Drug Act gives the government power to control the labeling of medicine.

Global Rationale: The Food, Drug, and Cosmetic Act, passed in 1938, prevents the marketing of drugs that have not been thoroughly tested prior to marketing. Drug companies are required to prove the safety and efficacy of any drug before it can be sold in the United States. The Public Health Service Act of 1944 covers many health issues, including biological products and the control of communicable diseases. The FDA Modernization Act is the largest reform effort of the drug review process since 1938. The Pure Food and Drug Act gives the government power to control the labeling of medicine.



nevelica

  • Hero Member
  • *****
  • Posts: 563
Both answers were spot on, thank you once again



yasmina

  • Sr. Member
  • ****
  • Posts: 323

 

Did you know?

More than 4.4billion prescriptions were dispensed within the United States in 2016.

Did you know?

Addicts to opiates often avoid treatment because they are afraid of withdrawal. Though unpleasant, with proper management, withdrawal is rarely fatal and passes relatively quickly.

Did you know?

During pregnancy, a woman is more likely to experience bleeding gums and nosebleeds caused by hormonal changes that increase blood flow to the mouth and nose.

Did you know?

Women are 50% to 75% more likely than men to experience an adverse drug reaction.

Did you know?

Approximately 70% of expectant mothers report experiencing some symptoms of morning sickness during the first trimester of pregnancy.

For a complete list of videos, visit our video library