Exam 1 Material Flashcards
What are the 3 important qualities of a medication?
Effectiveness
Safety
Selectivity
Besides the 3 main important qualities of a medication, what other properties do we look for?
Predictability
Ease of administration
Cheap
Shelf Stable
Simple generic name
reversibility
What are the factors affecting the intensity of drug responses?
Administration
Pharmacokinetics
Pharmacodynamics
Pharmacokinetics is?
What the body does to a drug
Ex: Absorption, distribution, metabolism, excretion
Pharmacodynamics is?
What the drug does to the body
Ex: Drug-receptor interaction, patient’s functional state, placebo effects
What are the 4 things that are involved in a nurse’s role as a patent educator?
Dosage and Administration
Minimizing adverse effects
Promoting therapeutic effects
Minimizing adverse interactions
What does the food and drug administration do?
-supervises development of new drugs
-Approves new drugs
-monitors safety of drugs on the market
What are the 3 steps in new drug development?
Pre-clinical testing in animals
Clinical testing
Post-market surveillence
All drugs have 3 names, what are they?
1)chemical
2)generic
3)brand/trade
What are the 5 rights of drug administration?
The right:
Patient
Medication
Dose
Route
Time
Documentation
Purple Mice Do Really Tiny Dances is to help remember?
The 5 rights of drug administration.
Patient Medication Dose Route Time Documentation
What are the 4 major processes in Pharmacokinetics?
Absorption, Distribution, Metabolism, Excretion
Both Pharmacokinetics and Pharmacodynamics both have sources of individual variation. What are some of these variables?
Physiological variables
Pathological variables
Genetic variables
Drug interactions
What are the 3 ways a drug is able to pass through a membrane?
Channels or pores
Transport system
Direct penetration of the membrane
In Pharmacokinetics, absorption involves the?
Movement of a drug from the site of administration INTO the blood
What are the factors that effect absorption?
Rate of dissolution
Surface Area
Blood Flow
Lipid solubility
The ______________ of absorption determines the intensity of effects
amount
The ________ of absorption determines the onset of effects (this can also be determined by route)
rate
What are the 3 common cateogories for routes of drug administration?
Enteral
Parenteral
Topical
Enteral route of drug administration is what? And what are these routes?
Enteral (by GI Tract)
PO by mouth
Enteral by feeding tube
SL sublingual
PR per rectum
Parenteral routes of drug administration is what? And what are these routes?
Parenteral (by injection)
IV intravenous
IM intramuscular
SC/SQ subcutaneous
Topical routes of drug adminstration are?
Inhalation
Ocular
Otic
transdermal
Drug Abbreviations:
AC
before meals
Drug Abbreviations:
HS
hour of sleep
Drug Abbreviations:
BID
twice a day
Drug Abbreviations:
TID
Three times a day
Drug Abbreviations:
STAT
immediatly
Drug Abbreviations:
PRN
as needed
Drug Abbreviations:
KVO
keep vein open
Drug Abbreviations:
NKDA
No known drug allergies
In Pharmacokinetics, distribution is?
The movement of a drug from blood INTO the cells
Distribution is determined by?
Blood flow to the tissues
Ability of drug to leave vascular system
Ability of drug to enter cells
For drugs to cross the BBB, they must be?
lipid soluble
What is the carrier protein for drug protein binding?
Albumin
Why can albumin not leave the capillaries?
It is too large to exit
If a drug is bound to albumin, can it exert it’s effects?
No, only ‘free’ drugs get to leave the capillaries and enter the cells, therefore exerting their effects
In Pharmacokinetics, Metabolism is
Biotransformation-the chemical alteration of a drug structure
Where does metabolism normally occur?
In the liver
Competition for which enzymes or changes in their activity can cause major drug interactions?
Cytochrome P450 System
The metabolism of a lipid-soluble to water soluble drug would give which effect?
increase renal drug excretion
What is an example of increased therapeutic action?
codeine to morphine
What is it called when a drug is inactive until it is metabolized?
activation of “prodrugs”
Acetaminophen to a toxic metabolite upon metabolization is an example of?
Increased toxicity
What is the first pass effect?
The rapid hepatic inactivation of certain oral drugs.
If a drug is known to undergo the first pass effect-how should it be administered?
Parentally
Malnutrition can effect drug metabolism, why?
Because many drugs need a number of cofactors to function. In a malnurished patient, these cofactors can be missing
If a drug is in enteroheptatic recirculation, what must it have undergone?
Glurcuronidation.
In Pharmokinetics, Excretion is?
The removal of drugs from the body
What is the main way drugs are excreted?
the kidneys through urine
What are some other not as common ways drugs are excreted?
bile, sweat, saliva, breast milk, and expired air
What are some of the variables to excretion?
pH dependent ionization
Competition for active tubular transport
age
kidney function
What are the 3 plasma drug levels?
Toxic concentration
Therapeutic range
Minimum Effect concentration
What is the half-life of a drug
the time required for the drug to decrease by 50%
What determines the dosing interval of drugs to maintain therapeutic levels?
The T1/2
(Half life)
How does one achieve a therapeutic plateau?
When the amount of drug eliminated between doses equals the dose administered, plateau will be maintained
Efficacy is?
the ability of a drug to do it’s job; the strongest effect that a drug can produce
Potency is?
amount to elicit a desired response; the dosage needed to produce effects
What would be an example of a time that a high efficacy wouldn’t be the right choice for a patient?
If a patient had a mild headache, morphine would not be the best choice of drug, even though it has a high efficacy. You want to match the intesity of the response with the patients needs.
An Agonist is a drug that?
ACTIVATES receptors
What is the method of binding for an agonist drug?
The bind to the receptor mimicking the body’s own molecules
A antagonist is a drug that?
Prevents or blocks a receptor; have no real effect on their own