Chapter 1-Intro Flashcards
Nurses Responsibility in regards to pharmacology (5)
- Administer drug
- Assess for side and adverse drug effects
- Make drug regimen more tolerable
- Providing patient teaching
- Monitor and prevent medication errors
Drug Actions (4)
- Replace or act as a substitute for missing chemicals
- Increase or stimulate certain cellular activities
- Depress or slow cellular activities
- Interfere with the functioning of foreign cells
Natural sources of drugs (2)
- Plants
- Animal products
Plant drug source description (2)
- Synthetic version of the active chemical found in a plant
- Main component of the growing alternative therapy movement
Animal product drug source description (2)
- Used to replace human chemicals
- Many of these are now made synthetically
Synthetic sources of drugs
Genetic engineering alter bacteria to produce chemicals that are therapeutic and effective
Drug Evaluation Steps (5)
- Preclinical Trials
- Phase I Studies
- Phase II Studies
- Phase III Studies
- Phase IV Studies
Preclinical Trials
- Chemicals are tested on lab animals
- Safety
Phase I Studies
- Chemicals tested on human volunteers
- Healthy people
Phase II Studies
-Drug tried on informed patients
-Phase III Studies
- Drug used in vast chemical market
- Deemed safe and effective
Phase IV Studies
- Continual evaluation of the drug
- Full marketing
When does full FDA approval occur
Between Phase III and Phase IV
What categories of medications are safe for pregnant women?
Category A and B
What category of medication causes fetal risk?
Category D and X
What medication category has no studies done on fetal risk?
Category C
What controlled substance has the highest abuse level?
Schedule I
What controlled substance have the least amount of abuse?
Schedule V
What is a generic drug?
Chemicals that are produced by companies involved solely in the manufacturing of drugs
Problems associated with OTC drugs? (3)
- Mask signs and symptoms of underlying disease
- Drug interactions
- Overdose if not taken correctly
What is on a drug label?
-Identification of the drug
-
What is a package insert? (3)
- Prepared by the manufacturer
- Contains all of the chemical and study information that led to the drug’s approval
- Difficult to understand and read
1938 The Federal Food, Drug, and Cosmetic Act
Created what is now known as the FDA
1983 The Orphan Drug Act
Designed to promote the development of drugs to treat rare diseases