Key terms Test 1 Flashcards

(52 cards)

1
Q

Intrathecally

A

delivered directly to the spinal cord

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2
Q

Sublingually

A

absorption of medication placed under the tongue

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3
Q

Intravenously

A

direct injection into the vein

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4
Q

Therapeutic index

A

most closely related to drug safety

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5
Q

Clearance rate

A

dependent on organ ability to extract blood from plasma

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6
Q

potency

A

threshold dose that produces give response

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7
Q

efficacy

A

dosage range over which drug has desired effect

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8
Q

volume of distribution

A

ratio of drug administered to concentration in the plasma

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9
Q

tissue permeability

A

highly lipid soluble molecules move more easily cross membrane

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10
Q

Oral administration

A

major site of drug metabolism in alimentary tract

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11
Q

liver

A

first pass effect- med goes from stomach to liver and is greatly reduced before reaching bloodtream

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12
Q

first pass effect

A

metabolism/destruction of a drug before reaching the site of action

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13
Q

half life

A

duration of compound activity in the body

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14
Q

antagonist drug

A

reversal of effect of acute drug overdose

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15
Q

drug hydrolysis

A

reaction that breaks compound into separate parts

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16
Q

Mu receptor antagonist

A

mechanism of action for a drug given to reverse opioid effects

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17
Q

NSAIDs

A

GI bleed

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18
Q

kidney

A

primary organ for excreting medications

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19
Q

IV drugs concern

A

increased risk of toxic dose

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20
Q

bioavailability

A

variability of drug in the bloodstream

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21
Q

agonist drug

A

increased synthesis of neurotransmitter molecules

22
Q

severity of effect

A

difference between side effect and adverse reaction

23
Q

cox-2 inhibitors

A

associated increased cardiac risk

24
Q

bioequivalency criteria

A

same side effects and pharmacodynamic profile (generic)

25
low platelet count
associated with bruising
26
adipose tissue
common site of medication storage
27
extended corticosteroid use
increased risk of fracture
28
decreased receptor sensitivity
prolonged increase in stimulation of various receptors
29
standard dose-response curve
shift left = less dose required to produce a response
30
vitamin D
improves calcium absorption from the gut
31
bisphosphonoates
treatment for osteoporosis
32
HRT (hormone)
decreased fracture-based mortality
33
osteopenic
low bone mineral density; T-score of 1-
34
hyperalgesia
excessive opiod exposure; increase in pain sensitivity
35
naloxone
treatment for opioid dependence/overdose (mu receptor agonist)
36
self-administration
patient controlled analgesia, bolus with dose limit
37
COX-2 selective
less GI irritation and bleeding (NSAIDS)
38
Tylenol
- acetaminophen (non anti-inflammatory - analgesic (pain reliever) - antipyretic (fever reducer) - gold standard for OA - works on CNS - efficacy, safety, low cost - side effect: liver toxicity
39
Ibuprofen
- NSAID - analgesic - anti-inflammatory - motrin/advil - antipyretic - anticoagulant - side effects: can damage stomach lining or digestive tract
40
COX 1
- can cause stomach/intestinal ulcers | - enzyme is predominantly found in endothelial cells in mucosal membranes
41
COX 2
- does not cause ulcers | - enzyme predominantly found in in inflamed tissue following infection, tissue damage, or injuries
42
bioavailability
the amount of med that makes it to the blood stream
43
time course concentrations
measureable concentration from dose over time
44
loading dose
higher dose to speed time to therapeutic range
45
maintenance dose
dose to sustain desired therapeutic response
46
therapeutic drug monitoring
monitoring plasma concentration of med to determine if in desired range
47
distribution
where the med goes once in the body
48
volume of distribution
how much med is where in the body
49
concentration
amount of med in the plasma
50
cumulative effect
more pronounced effect with repeated dosing
51
target concentration
usually pertinent for NTI meds
52
steady state
same dose will result in same concentration over time.