pharmokinetics/pharmodynamics (Faith's set)

pharmokinetic

what our body does to meds

pharmokinetic phases

absorption
distribution
metabolism
excretion

drug absorption

drug movement from GI tract into bloodstream

disintegration

breakdown of oral drug into small particles

dissolution

combining small particles w liquid to form soltion

factors affecting absorption

Blood circulation
Pain, stress
Food texture, fat content, temperature
pH
Route of administration

how drugs get from GI tract to liver

via portal vein

bioavailability

how fast drugs get into blood stream

best bioavailability route

IV

best ORAL bioavailability form

liquid

worst bioavailability route

enterocoated meds

first pass effect

drug gets broken down in GI tract and concentration is reduced before it gets into blood stream

how to avoid first pass effect

give meds IV or IM

factors affecting bioavailability

drug form/route
gastric mucosa/motility
giving w food/other meds
change in liver metabolism (bad liver-cant metabolize-stays in system)

primary organ for drug metabolism

liver

are protein bound drugs active or inactive

inactive

are free/not protein bound drugs active or inactive

active

high protein bound drugs are what % bound

over 90%

what part of the drug is active

the unbound part

what happens if u give dilantin (99% bound) and warfarin (90% bound) together

fight for protein and dilantin would push off warfarin (causing warfarin toxicity)

what happens if u dont get enough protein in ur diet

protein bound meds are free and active and u can easially get toxic

half life

how long it takes for 50% of a med to be eliminated

if u give 650mg of a med at 8am and it has a 4h half life, how much is in ur syst at noon

325mg

loading dose

large initial dose of a med w long half life so u get relief faster (digoxin)

whats the main way drugs are excreted

kidney

what happens if the kidneys arent working

cant excrete drug and it builds up in system causing toxicity (monitor BUN, creatinine, GFR)

primary drug effect

desired effect/what its perscribed to do

secondary drug effect

side effecr that can be desireable or undesireable (benadryl also makes u sleepy so give for allergies but also helps sleep)

drug potency

amount of drug needed to elicit a specific physiologic response (high-big response from low dose)

theraputic index (TI)

relationship between therapeutic dose and toxic dose (shows risk for toxicity)

narrow theraputic index

high risk for toxicity (vancomycin, digoxin, dilantin, warfarin)

when do u draw lab to test for peak

1h after giving med

when do u draw lab to test for trough

right before next dose is due (first dose should be out of system)

onset

how long after u give med will u get some effect

peak level

when its at its highest amount (too high-toxic, too low-not working)

duration

how long does med last

trough

lowest blood concentration, draw right before nect dose (high-very likely for toxicity)

agonist

gives u action u want fom med

antagonist

blocks action of something

nonspecific drugs

binds to MULTIPLE SITES
wherever the same type of receptor is, you get same reaction at all those sites (anticholinergics dry up mouth and eyes and retain urine)

nonselective drug

binds to MULTIPLE RECEPTORS
(epinephrine-increase bp/hr, opens airway)

adverse reaction

unintentional and unexpected severe side effect

pharmacogenetics

study of genetic factors influencing indicated resposne

tolerance

decreased response over time
if u take med all the time, eventually effect decreases so u require more

tachyphylaxis

very fast/acute decrease in drug responsiveness

placebo

drug response not expected from drug (pt thinks tylenol makes them drowsy)

drug interaction

alteration of drug effect that occurs inside person

drug incompatability

chemical/physical reaction b/t drugs that occurs in syringe or IV site

drug nutrient

enzymes that work as drug enhancer or inhibitor (grapefruit juice)

drug nutrient enhancer

lower drug effectiveness (ineffective)

drug nutrient inhibitor

increase drug effectivenss (toxicity)

photoallergic

skin reaction caused by light exposure
slower immune mediated response

phototoxic

fast skin reaction caused by light exposure (2-6hrs)

additive

2 meds work together and get combined effect

synergistic

give 2 meds together and get hella strong reaction (more than just 2 combined)

antagonistic

give 2 drugs and one reduces/blocks the effect of the other