Module 2 Map Overview Chap 1 Consumer Safety and Drug Regulation
Objectives:
Chapter 1
- Learn to navigate the course
- Understand expectations of the course
- Review the syllabus and schedule
- Explain what is meant by drug standards.
- Name the main drug laws passed in the United States concerning consumer safety and standardization.
- Define the schedules of controlled substances.
- Explain what is meant by DEA number and the NDC directory.
- Interpret what is meant by USP/NF.
- State the responsibilities you have in administering medications.
Let's begin our journey into the world of pharmacology.
In order to navigate this course, the best recommendation that I can give you is to make sure you read the textbook chapters, read any additional content lesson pages provided, try the practice problems and games before attempting the Putting it All Together and Learning Labs. Once you have completed all of the homework assignments and practice games, then complete the Final Chapter Test.
You have many practice games that are optional, but will also test your understanding of the material. I recommend you try the practice games before doing the chapter tests.
So, what's in chapter 1?
In this chapter, you will briefly look at the legal history of consumer drug safety and it's impact on health and society. The main focus of this chapter is the introduction of many of the important drug laws that have been enacted over the last 100 years. These laws not only control the safety and distribution of drugs, but also regulate the entire process from establishing the standards in the making of drugs, to the rules determining who can prescribe and/or dispense medications, to the drug's final destination at the hands of its intended patient.
Since you are in this class, you will probably have patients or clients someday in the future. The drug laws we are covering in this chapter will directly impact how you practice healthcare with your patient or client.
Read Chapter 1 on Consumer Safety and Drug Regulations.