pharmacology quiz 2 Flashcards

1
Q

pharmacokinetics

A

the motion/movement of drugs in your body

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2
Q

pharmacokinetics process

A

absorption
distribution
metabolism
excretion

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3
Q

absorption

A

the movement of a drug from its site of administration into the blood

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4
Q

the rate of absorption determines ____

A

how soon the effects will take place

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5
Q

the amount of drug determines ____

A

how intense the effects will be

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6
Q

factors affecting absorption process (6)

A

-rate of dissolution
-surface area
-blood flow
-lipid solubility
-pH partitioning
-route of administration

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7
Q

routes of administration (2)

A

enteral (GI tract)
parenteral (outside GI tract)

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8
Q

enteral (GI tract)

A

oral (by mouth/PO)

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9
Q

parenteral (outside GI tract)

A

Intravenous (IV)
subcutaneous (subQ)
intramuscular (IM)

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10
Q

oral, by mouth, PO barriers to absorption

A

epithelial lining of GI tract

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11
Q

oral absorption patterns

A

slow and variable

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12
Q

advantages of PO meds (3)

A

-safer than injections
-ideal for self administration
-easy,convenient, cheap

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13
Q

disadvantages of PO meds (4)

A

-GI irritation
-requires cooperative pt
-inactivation
-variability

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14
Q

intravenous (IV) barriers to absorption

A

none

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15
Q

IV absorption pattern

A

instantaneous and complete

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16
Q

advantages of IV (4)

A

-rapid onset
-control
-permits use of large fluid volumes
-permits use of irritant drugs

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17
Q

disadvantages of IV (4)

A

-high cost, difficulty, inconvenience
-irreversibility
-infection
-high risk

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18
Q

intramuscular (IM) and subcutaneous (subQ) barriers to absorption

A

none

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19
Q

IM and SubQ absorption pattern

A

VARIABLE
-water solubility
-blood flow

20
Q

advantages of IM and SubQ (2)

A

-can be used for poorly soluble drugs
-can be used for depot preparations

21
Q

disadvantages of IM and subQ (4)

A

-discomfort
-inconvenience
-can cause muscle and nerve injury with improper technique
-bleeding risk

22
Q

when parenteral administration is preferred: (6)

A

-emergencies
-situations requiring tight control
-GI incompatibility
-treatment with drugs that cannot cross membranes
-condition better treated with long-acting preparation
-pts who cannot or will not take oral preparation

23
Q

distribution

A

the movement of drugs throughout the body

24
Q

distribution process

A

-blood flow to tissues
-drug’s ability to enter cells
-drug’s ability to exit the vascular system

25
drug metabolism
the enzymatic alteration of drug structure to a more water-soluble form that can be excreted
26
special factors/considerations in drug metabolism
-age -first-pass effect -nutritional status -competition between drugs
27
excretion
the removal of drugs from the body
28
excretion routes
-bile -urine/feces -sweat/saliva -breast milk -expired air
29
monitoring of drug responses plasma drug levels
correlation between response to drug and level in plasma
30
monitoring of drug responses two important levels
-minimum effective concentration (MEC) -toxic concentration
31
monitoring of drug responses therapeutic range
determines whether the drug can be safely given
32
monitoring of drug responses drug half-life
determines dosing interval
33
monitoring of drug responses repeated dosing
determines rate and extent of accumulation
34
peak
highest level of drug in the body, 1-2 hours after given
35
trough
lowest level of drug in body, right before next dose
36
maintenance
lower dose to maintain state of drug in body
37
loading
higher dose to get response
38
ED50
average effective dose
39
LD50
lethal dose
40
pharmacodynamics
the force or power of a drug
41
drug drug interactions outcomes (3)
potentiate inhibit new response
42
potentiate
intensifies the effects
43
inhibit
reduce the effects
44
new response
effect not seen with single drug alone
45
drug v food (5)
-absorption -drug metabolism -drug toxicity -drug action -timing