Chapter 3+4 Flashcards
1
Q
what are the routes?
- PO
- SL
- SC, SQ
- ID
- IM
- IV
- PR
- INH
- TD
A
- oral
- sub-lingual
- subcutaneous
- intradermal
- intramuscular
- intravenous
- anal
- aerosols
- transdermal
2
Q
what is pharmacokinetics?
A
- study of drug movement throughout the body
- –> absorption
- –> distribution
- –> metabolism (biotransformation)
- –> excretion (elimination)
3
Q
what is pharmacodynamics?
A
- drugs affects on the body
- –> receptor binding
- –> post-receptor effects
4
Q
what is the first pass effect?
A
- large portion of the drug is not used
5
Q
what are factors that affect drug distribution?
A
- circulation to tissues
- blood-brain barrier
- protein binding
6
Q
what is protein binding?
A
- drug molecules attach to proteins creating drug-protein complex enabling the drug molecules useless
7
Q
which organ biotransformation the drug?
A
- the liver
8
Q
what is cytochrome p-450 (CYP)?
A
- the enzyme the liver uses to break down drugs
- some drugs are CYP inhibitors: inhibit the liver enzyme which can prevent the breakdown of drugs
- some drugs are CYP inducers: increases the production of CYP requiring higher dose of drugs
9
Q
what fruit inhibits CYP?
A
- grapefruit
10
Q
what is Ativan’s half-life?
A
- 12 hours
11
Q
what is excretion and how are drugs excreted?
A
- elimination of drugs from the body —> through the kidneys
12
Q
what is pharmacodynamics?
A
- the way the drug affects the body
—> Primary effect: desired response
—> Secondary effect: desirable (ex. viagara) or undesirable (ex. heartburn)
13
Q
what is onset?
A
- time it takes for drug to reach effective concentration
14
Q
what is peak?
A
- highest concentration in blood
15
Q
what is duration?
A
- amount of time effects of the drug last for