pharmacology quiz 2 Flashcards

1
Q

Pharmakon means

A

drug or poison

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2
Q

kinesis means

A

motion

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3
Q

process through the body

A

absorption, distribution, metabolism, then excretion

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4
Q

pharmacokinetics is _____

A

how drugs move through the body

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5
Q

drug coming into the body is ___

A

absorption

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6
Q

most common way the drug is absorbed through the body is through the _____

A

GI tract

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7
Q

our ____ is how that drug gets distributed

A

blood

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8
Q

primary organ for metabolism

A

liver

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9
Q

_____ do a little bit of metablism

A

kidney

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10
Q

kidney excretes by how ____

A

urine

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11
Q

liver excretes by how ___

A

bile

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12
Q

____ of absorption determines how soon effects will take place

A

rate

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13
Q

____ of drug determines how intense the effects will be

A

amount

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14
Q

quicker drug dissolves, the quicker we see effects is known as ____

A

rate of dissolution

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15
Q

larger the _____, the quicker the absorption of the drug

A

surface area

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16
Q

patient’s who have better ____ ____ are going to have quicker/better absorption

A

blood flow

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17
Q

if a drug is ____ _____, it is absorbed more quickly because our cellular membranes are made up of lipids

A

lipid solubility

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18
Q

two major groups for route of administation

A

enteral gastrointestinal tract (GI tract) and parenteral (outside of the GI tract)

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19
Q

enteral (GI tract)

A

oral (PO) medications

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20
Q

parenteral (outside the GI tract)

A

is faster than through the GI tract, so IV, subcutaneous, intramuscular

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21
Q

_____ is the fastest route of absorption

A

intravenous (IV)

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22
Q

advantages of oral (PO)

A

safer than injections, ideal for self-administration, and is easy/convenient/inexpensive

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23
Q

disadvantages of oral (PO)

A

can cause GI irritation, requires cooperative patient, inactivation, variability (each pt metabolizes drug differently)

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24
Q

absorption pattern of oral (PO)

A

slow and variable

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25
barriers to absorption (oral)
epithelial lining of GI tract and capillary wall
26
advantages of IV
rapid onset, control, permits use of large fluid volumes, and permits use of irritant drugs
27
disadvantages of IV
high cost, difficulty, inconvenience, irreversibility, infection, high risk
28
barriers to absorption of IV
none
28
absorption pattern of IV
instantaneous and complete
28
advantages of IM and subQ
can be used for poorly soluble drugs and can be used for depot preparations
29
depot preparations means
when we give an IM injection one time and it activates for several months
30
disadvantages of IM and subQ
discomfort, inconvenience, can cause muscle and nerve damage injury with improper technique, bleeding risk
31
barriers to absorption for IM and subQ
none
32
absorption pattern for IM and subQ
variable, water solubility, and blood flow
33
when is parenteral administration is preferred?
emergencies, situations requiring tight control, GI incompatibility (drugs that are destroyed by GI system or cause GI injury), treatment with drugs cannot cross membranes, condition better treated with long-acting preparation, patients who cannot or will not take oral preperation
34
_____ is the movement of drugs throughout the body and dependent on blood flow
distribution
35
distribution process
blood flow to tissues, drugs ability to enter cells, and ability to exit the vascular system
36
___ ____ is the enzymatic alteration of drug structure to a more water-soluble for that can be excreted
drug metabolism
37
certain drugs that are completely metabolized by the liver the first time they pass through the liver
first-pass effect
38
_____ is the removal of drugs through the body
excretion
39
drugs and their metabolites can exit the body through
bile, urine/feces, sweat/saliva, breast milk, and expired air
40
two important levels of monitoring of drug responses
minimum effective concentration (minimum point where a drug effects a patient) and toxic concentration (too high can kill a patient)
41
therapeutic range (positive)
determines whether the drug can be given safely (between MEC and toxic concentration)
42
drug half-life
amount of time for the % of drug in a body to decrease by 50%
43
repeated dosing means
how a medication plateaus
44
highest amount of drug in the body, 1-2 hours after the last dose is the ____
peak
45
lowest amount of drug in body, seconds before next dosage
trough
46
loading drug is ___
tapering drug
47
pharmacodynamics is ___
force or power of drug
48
relationship between the size of an administered dose and the intensity of the response produced is ___
dose-response relationship
49
ED50 ___
average effective dose
50
LD50 __
lethal effective dose
51
minimum amount of drug needed to elicit a response
relative potency
52
maximum response a drug can elicit
maximum efficacy
53
intensifies the effects
potentiate
54
Reduces the effects
inhibit
55
effect not seen with single drug use
new response
56
what fruit decreases metabolism of certain drugs, meaning drugs can stay in body longer
grapefruit
57
empty stomach is when
1 hour before or 2 hours after a meal
58
-erol
SABA- short acting beta-agonist
59
fast acting/rescue inhaler
bronchodilator
60
fluoroquinolones
levofloxacin (levaquin) or ciprofloxacin (cipro)
61
fluoroquinolone is great for what?
bacterial respiratory infections
62
side effects of fluoroquinolones?
joint pain, clostridium difficile, liver toxicity, renal failure, prolonged QT syndrome, and achilles tendon rupture
63
corticosteroids
reduce inflammation and suppress the immune system
64
corticosteroids you must never do what?
stop abruptly and requires weaning
65
corticosteroids can decrease what swelling of ____
kidneys