Lecture 1 - Intro Flashcards

1
Q

Potential for drug-receptor binding.

A

Affinity

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2
Q

Binding site w/ biological effect.

A

Receptor

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3
Q

Capacity to produce a biological effect.

A

Intrinsic activity

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4
Q

Having intrinsic activity and affinity.

A

Agonist

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5
Q

Affinity without intrinsic activity.

A

Antagonist

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6
Q

A stereospecific phenomenon whereby a bound ligand influences specificity of a second site

A

Allostery

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7
Q

Efficacy

A

[affinity] x [intrinsic activity]

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8
Q

‘effective’ concentration in 50% of subjects

A

EC50

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9
Q

‘effective’ dose in 50% of subjects

A

ED50

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10
Q

‘inhibitory’ concentration in 50% of subjects

A

IC50

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11
Q

Result in chronic antagonism.

A

hypersensitivity

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12
Q

minimum amount of drug producing maximum therapeutic effect

A

maximum dose

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13
Q

Low intrinsic activity with potency and affinity within therapeutic range.

A

partial agonist

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14
Q

Drug –> Body

A

Pharmacodynamics

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15
Q

Body –> Drug (ADME)

A

Pharmacokinetics

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16
Q

Drug –> Disease

A

Pharmacotherapeutics

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17
Q

Science of drug dosing

A

Posology

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18
Q

response to a give dose

A

Potency

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19
Q

Loss of pharmacological effect.

A

Resistance

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20
Q

Ability to produce a desired effect versus adverse effect.

A

Selectivity

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21
Q

Ability to act at a specific receptor.

A

Specificity

22
Q

Rapidly decreasing therapeutic response.

A

Tachyphylaxis

23
Q

congenital malformation

A

Teratogenesis

24
Q

Amount of active drug reaching target tissue.

A

Bioavailability

25
LD50:ED50 or TD50:ED50
therapeutic index
26
Diagnostic pharmaceutical agent
DPA
27
Therapeutic pharmaceutical agent
TPA
28
insulin
Supplemental drug type
29
glucose
Supportive drug type
30
low dose aspirin
Prophylactic drug type
31
fluorescein
Diagnostic drug type
32
Methotrexate
Therapeutic drug type
33
Tear film
~10ul
34
max surface area
~30 ul
35
gt?
25-56 ul
36
Basal tear flow
0.5-2.2 ul/min
37
cornea in diabetes
thick
38
cornea in keratoconus
thin
39
Concentration independent; rate limiting barrier or saturable carrier; constant amount of clearance; elimination per unit time is linear
Zero order
40
Concentration dependent; non-saturable carrier; constant proportion of clearance & constant half-life; elimination per unit time is exponential
1st order (most drugs)
41
saturable carrier at high concentrations only
mixed-order
42
High abuse, no known medical use, lack of safety
Schedule 1 Drug; unavailable like heroin
43
High abuse, some medical use, high risk of dependency
Schedule 2 Drug; morphine
44
Lower abuse, medical use, moderate dependency risk
Schedule 3 Drug; valium
45
Limited abuse, high medical use, limited dependency risk
Schedule 4 Drug; codeine
46
Minor problems, may be available w/o Rx
Schedule 5 Drug; penicillin
47
No evidence of risk in women.
A
48
No evidence of risk in animals.
B
49
Animal toxicity evidence
C
50
Risk may equal benefits
D
51
Risk > benefits
X
52
Off-label drug use
Practice of prescribing a drug for a non-FDA approved indication