Week 1: intro and cells/immune system Flashcards
generic name-where is it categorized and what is it, example
-in pharmacies, this is how it is categorized
-medicine’s active ingredient that makes it work
-nonproprietary
-ex. ibuprofen
trade name
name of company
- proprietary name
- advil
what are the 3 types of drug names
chemical
generic
trade
what are the 5 pharmacological priniciples
pharmaceutics
pharmacokinetics
pharmacodynamics
pharmacotherapeutics
pharmacognosy
what are the 3 phases of drug activity
pharmaceutical phase
pharmacokinetic phase
pharmacodynamic phase
what occurs during the pharmaceutical phase
disintegration of dosage form
what occurs during the pharmacokinetic phase
absorption, distribution, metabolism, excretion
what occurs during the pharmacodynamic phase
drug-receptor interaction
why is drug absorption generally slower in young and the elderly
less gastric juices
what can increase and decrease absorption depending on the situation
food
pharmacokinetics…determines what and when it is
determines how it goes up/down and how fast it goes into you
*whenever you are told to take something with food
drug absorption of various oral preparations…fastest to slowest
liquids, elixirs, syrups
suspension sol’n
powders
capsules
tablets
coated tablets
enteric-coated tablets
pharmacokinetic phase is the process of…and what are the 4 things
drug movement to achieve drug action
1. absorption
2. distribution
3. metabolism
4. excretion
pharmacokinetic phase: absorption. this is the process of
the drug leaving the site of administration and becoming available
what is the main purpose of the pharmacokinetic phase, what does it require, what is most important here
-wants meds to be available
-requires food and fluids
-rate of blood flow to the small intestines and the acidity of the stomach is most important here
what factors affect absorption: pharmacokinetic phase(examples and were is it absorbed)
*most oral drugs are absorbed into the surface area of the small intestine
- how drug was delivered
-the food and fluids that were given with the drug
- dosage formulation
- status of the absorptive surface
- rate of blood flow to the small intestines
-acidity of the stomach
- status of GI motility
first pass effect…what is it, where, practical application
- anything that comes into the body goes through the liver and it potentially metabolized
- only occurs when the GI tract is involved
- the reason why ppl get such a high dose of drugs is because the majority of the medication is metabolized by the liver. more drug you give, the faster the liver gets rid of it
official definition of first pass effect
the metabolism of a drug and its passage from the liver into the circulation
ways to bypass the liver-pharmacokinetic phase
sublingual
buccal
rectal
intravenous
intranasal
transdermal
vaginal
intramuscular
subcutaneous
inhalation
when bypassing the liver what route undergoes a higher degree of first-pass effects
rectal
when do you use the various methods of bypassing the liver: rectal
helpful when pl can’t swallow
when do you use the various methods of bypassing the liver: intranasal
mostly recreational
when do you use the various methods of bypassing the liver: transdermal
patch: slow process
24-48 hours before the drug will work
when do you use the various methods of bypassing the liver: sublingual
used commonly for panic attacks, short term solution, quick acting
when do you use the various methods of bypassing the liver: intramuscular and subcutaneous
gives diff flow of meds
when do you use the various methods of bypassing the liver: inhalation
delivers drugs you want to the place the injury is, gets less side effects because you don’t need as many meds
when do you use the various methods of bypassing the liver: subcutaneous
subcutaneous port: for pain pump, pain relief long term if the patient can’t handle oral
when do you use the various methods of bypassing the liver: intravenous
terrible for chronic pain because its fast acting
pharmacokinetics: distribution, what is it, what is it influenced by and why is it important
-drugs are distributed throughout the body by the bloodstream (circ system)
- influenced by: blood flow, affinity to the tissues, protein-binding, volume of drug distribution
- differential blood flow can change the effectiveness of the drug
pharmacokinetics: metabolism, where, whats it called and what enzyme
liver, biotransformation
cytochrome P-450 enzymes
what does the p-450 do
makes it easy for the body to find it and get rid of it
makes it water soluble
what are hepatics biotransformations
variations of p-450
when do people use renal dosing
for ppl in renal failure bc it will stay in their body, bc they can’t eliminate
pharmacokinetics: excretion, what does it mean, what organ, other routes
-elimination of drugs from body
- kidney-main organ
-liver, bile feces, lungs, saliva, sweat and breast milk
pharmacokinetics: half life of a drug…what effects it, what is it useful for, how it is determined
-metabolism and elimination affects it
- useful for determining ‘steady state’
- determined on how fast your liver works/how effective your kidney is
after 5 half-lifes what does that mean for the drugs
that there is effectively 0 drugs
what is a steady state, why is it important, used for what
-for chronic meds
- same amount of drug floating around at the same time (drug eliminated=drug absorbed)
-achieve a therapeutic effect
pharmacodynamics…what is it
what the drug does to people
pharmacodynamics: mechanisms of actions
-receptor interaction: reactive site allows (agonist) or blocks (antagonist) physiological response
- enzyme interaction: drug inhibits/alters physiological response of an enzyme
- non-specifics interaction: drugs interfere with or chemically alter cellular/metabolic processes
pharmacotherapeutics: nursing responsibility-assessment
current meds, pregnancy, illnesses, allergies, sensitivities, contraindications
pharmacotherapeutics: nursing responsibility- implementation
intent of the therapy, psycho-motor skill of administering
pharmacotherapeutics: nursing responsibility-monitoring
client’s condition (therapeutic effect), side effects, adverse effects/rxns, toxic effects: all drugs capable, interactions