Week Two Flashcards

(71 cards)

1
Q

the movement of how a drug moves throughout the body

A

pharmacokinetics

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2
Q

what are the two main points regarding pharmacokinetics

A
  • trying to achieve maximum benefit of medication without causing harm
  • intensity of medication
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3
Q

what questions should come to mind when dealing with pharmacokinetics

A

how does drug get into body and where does it go?
what does the body do with the drug?
how does the body get rid of the drug

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4
Q

what is the process of pharmacokinetics through the body

A

absorption
distribution
metabolism
excretion

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5
Q

going into blood stream=

A

absorption

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6
Q

going to tissue and cells=

A

distribution

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7
Q

metabolized in liver by enzymes=

A

metabolism

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8
Q

taken out of the body=

A

excretion

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9
Q

what is determined with the process of pharmacokinetics in the body

A

intensity of the drug to its intended site of action

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10
Q

what is the objective of pharmacokinetics

A

we want the highest level of intensity to create maximum benefit without harm

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11
Q

what is the biggest organs to excrete medication

A

through kidneys, bowel and air we breathe

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12
Q

what are the three passages of drugs across membranes

A
  • channels and pores
  • transport system
  • direct penetration of the membrane
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13
Q

what is the definition of transport system

A

one side of cell membrane to the other

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14
Q

what is one of the larger transports and multi drug transporter protein,

A

P-glycoprotein

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15
Q

what 5 places is the P-glycoprotein found in

A
  • liver
  • kidney
  • intestines
  • placenta
  • capillaries of brain
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16
Q

why is P-glycoprotein important for excretion

A

because it reduces chance of toxicity in medication

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17
Q

movement of drug from site of administration into the blood

A

absorption

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18
Q

what does the medication have to do in order to be absorbed

A

dissolved

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19
Q

what factors can affect process of absorption

A
  • rates of dissolve and absorption
  • surface area
  • blood flow
  • lipid solubility
  • pH levels
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20
Q

the _______ the surface area the _______ medication can be absorbed

A

larger;faster

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21
Q

what are most drugs

A

lipid soluble

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22
Q

what routes can affect drug absorption

A

IV, IM, Oral

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23
Q

what are the advantages/barriers of IV route

A

advantage: directly into blood stream
barrier: no barrier, absorption is immediate

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24
Q

what are the advantages/barriers of IM route

A

advantage: food for poorly soluble medication, deposited into certain parts of body
barrier: capillary walls and muscle are, won’t get to the body as fast as IV

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25
what are the advantages/barriers of oral route
advantages: simple to administer, convenient, less expensive, pt compliance barrier: stomach, intestines, competing with other meds
26
what is the fastest route to get meds where needed
IV
27
drug distribution is determined by what 3 factors
- blood flow to tissues - exiting the vascular system - entering the cells
28
for best distribution process what does the meds need
need to be lipid soluble and need transport system
29
when is medication delayed
when having to get through blockage such as a tumor
30
what drugs can cross the blood brain barrier (BBB) to a significant degree
drugs that are lipid soluble or have a transport system
31
why is BBB important
this protects brain from medications
32
what is the mixed blessing of BBB
protects brain from toxic substances but also blocks certain meds needing to treat CNS disorders
33
where is BBB not really developed
at birth
34
what are characteristics of placenta membranes
- lipid soluble meds pass readily | - P-glycoprotein bound meds are largely excluded
35
what are the risks with placenta drug factors
could cause defects, dependency and respiratory issues in baby
36
if mother needs surgery or given meds such as analgesic what are the risk factors in baby
respiratory depression
37
membranes of the placenta ___ ____ constitute an absolute barrier to the passage of drugs
do NOT
38
plasma albumin is _______ and important for drugs to _____ to
abundant; bind
39
why is it important for drugs to bind to albumin
since it is so large it remains in blood stream and plays role in healing
40
how does albumin impact drug distribution
doesn't allow certain meds to reach intended site, cause for drug interaction because it is so big
41
what happens when binding sites compete for drug distribution
intensity is increased then patient can become toxic
42
what helps with drug metabolism
enzymes
43
where does metabolism take place
liver
44
what can enzymes activate
prodrug= medication that remains inactive until it has been affected by metabolism of one of these enzymes
45
what are the special factors/considerations in drug metabolism
age first-pass effect nutritional status competing between drugs
46
drugs and their metabolites can exit (excrete) the body through
- bile - urine/feces - sweat/saliva - breast milk - expired air
47
what is the most important organ typically involved with excretion
kidneys and liver
48
what is the importance of plasma drug levels
make sure that there is a correlation between therapeutic level and toxic level
49
what are the two important levels of time course of drug responses
- MEC=drug level that falls below level of therapeutic action - Toxic concentration
50
what is the therapeutic range purpose
make sure medication doing what its supposed to and is it given at a safe level
51
what is drug half life
time required for amount of drug in body to be decreased by 50% (important because determines drug dosing interval)
52
build up in body of repetitive dose
plateau
53
how many days does it take to achieve plateau
5
54
medication at its highest level in the body
peak (1-2 hrs after last dose)
55
trough is right before the next dose is _____
scheduled (30 minutes)
56
loading is when
prescriber tells you to start off with 2 medications or more at one time and then take less the next day
57
when finished with medication why is it important to know the outcome
know results and how long the medication is going to last and what is equally important is what meds have been discontinued
58
drugs typically take how long to leave the body
4-5 days
59
study of what drugs do to the body and how they do it
pharmacodynamics
60
what is the dose response relationship in pharmacodynamics
relationship between the size of the dose and intensity of the response produced determines relative potency and is minimum amount of drug needed to illicit drug response
61
in pharmacodynamics we want maximal efficacy which is
maximum response at the smallest dose
62
measures drug safety by using lab animals, the ratio of the drugs legal dose to its effective dose tested on lab rats
therapeutic index
63
highest dose of therapeutic index=
safer the drug is
64
smaller dose of therapeutic index=
less safe the drug is
65
when patient takes more than one drug there will be some sort of interaction
drug-drug interaction
66
consequences of drug-drug interactions
it can potentiate (increase therapeutic effect) or increase adverse effect or reduce adverse effects or therapeutic effects
67
what is the drug to drug unique response
two drugs creates something that would not be seen if given individually
68
who is at greater risk of drug to drug interactions
young, old, kidney and liver failure, multiple medications, pregnant women, chronic illnesses
69
ways to minimize drug-drug interaction
knowing history ask about drug history and what is being taken be aware of the possible of toxicity adjust timing because it can affect with food monitor for early signs of narrow therapeutic index
70
what juice greatly inhibits metabolism of certain drugs by raising blood level which makes pt toxic
grapefruit juice
71
who long can grapefruit stay in persons system
3 days since last dose