Week 1: Intro to Pharm Flashcards
Characteristics of an Ideal Drug
- Effective
- Selective
- Reversible
- Predictable
- No harmful side effects
- No drug/food interactions
- Inexpensive
- Easy to administer
- Chemically stable
- simple name
*There currently are NO ideal drugs
Objective of drug treatment
Maximum Benefit with minimum harm
Education to Patient and family about Medications
- Medication name
- expected respone; possible side effects
- dosage and administration schedule
- route of administration
- duration of drug use
- drug storage
Pharmacokinestics:
define/the 4 steps
- How drugs can move through the body
1) Absorption
2) Distribution
3) Metabolism
4) Excretion
Pharmacotherapeutics:
The use of drugs to….
1) Diagnose
2) Prevent disease
3) Treat disease
4) Prevent pregnancy
5 Rights to give medication
1) Right drug
2) Right dose
3) Right time
4) Right patient
5) Right route
Pharmacokinetics:
Absorption
- from site of administration into bloodstream.
- rate determines how soon effects occur
- amount determines intensity of effects
- effecting: ph, had food or not, pain, stress, rate of gastric empyting
Lipid soluable drugs tend to be _______ and hang around _________ than water soluable drugs
stored in fat, longer
Passive absorption
diffusion…higher to lower concentration..no energy needed
Active Absorption
needs carrier or enzyme to move across membrane
Pinocytosis
cell engulfs particles of drug
disintegration
and
dissolution
disintegration- brode down into small particles
dissolution- dissolving into smaller particles
Factors affecting drug absorption
1) Rate of dissolution
2) Surface area
3) blood flow
4) lipid solubility
5) Food or fluids taken along with drugs (some meds will be slowed down with food and drink while some need it)
Routes of Administration
1) Enteral– gut,mouth, peg tube, gtube, rectal (Absorbed through oral or gastric mucosa, small intestine or rectum)
2) Topical
3) Parenteral –IV, IM, SQ
Distribution
Define/distribution effected by:
-How it moves/gets through the body..movement of drug throughout the body through the circulatory system
effected by:
-bloodflow to tissues
- ability of drug to exit the vascular system
- ability of drug to enter cells
_*determined by how well med can enter the cells*_
Drug diffuses out of blood to ___________
the site of action
blood brain barrier
- tight junction between cells of capillary walls in the CNS
- only drugs that are lipid soluable or have a transport system can cross through the capillary walls to the CNS
- Benefits: very specific on what crosses, can protect the brain from drugs and harmful substances
- Disadvantage: obsticale treating seizures, cancers in brain or parkinsons
Protein Binding
- Type of drug storage system
- Drugs form reversible bonds with protein
- drugs NOT bound to protein are a FREE state and are still active
- drugs bound to protein are NOT active
- As free drug acts on cells, there is a decrease in plasma drug levels
- need to know pts albumin level
- two highly bound protein bound drugs will compete and one will become toxic
highly protein bound
moderately protein bound
low protein bound
- 80-90%
- 50%
- 10-20%
Metabolism
- “Biotransformation”
- converting a drug to a form more easily removed from the body
- Almost all occurs in liver
- Hepatic microsomal enzyme or P450
Conjugates
make drugs more water soluble and more easily excreted by the kidneys
P450
- a way that a drug is metabolized
- enzyme from the liver which aid in metabolism of many drugs
- Initiate drugs, accelerate excretion
Drug to drug interations involving P450
- inhinitor works against enzyme
- inducer makes more enzymes available
Factors Influencing rate of metabolism
- age
- nutritional status
- liver disease
- induction of drug-metabolizing enzymes
- first pass effect
