module 1 synch Flashcards

1
Q

pharmacodynamics

A

what the drug does to the body

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2
Q

pharmacokinetics

A

what the body does to the drug

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3
Q

pKa

A

half of drug concentration ionized, half non-ionized

- basic drug in base will stay together

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4
Q

nonionized, lipophilic drugs favored for

A

oral absorption

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5
Q

weak acids best absorbed

A

in stomach

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6
Q

weak bases are best absorbed

A

in small intestine

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7
Q

drugs with low Vd may be

A

highly protein bound and more likely to remain in plasma

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8
Q

induction and substrates (CYP450)

A

drugs that are substrates are generally more rapid and extensively metabolized
- reduce concentrations -> dec. drug effect of substrate drug

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9
Q

inhibition and substrates

A

will generally increase plasma concentrations of drugs that are substrates
- inc. drug effect and possibly toxicity of substrate drugs

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10
Q

CYP450 induction

A

inc. production of enzyme
dec. degradation
induction by another drug or autoinduction

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11
Q

cyp450 inhibition

A

incidental or deliberate
competitive inhibition
irreversible inhibition

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12
Q

full agonist

A

activates receptor with maximal efficacy

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13
Q

partial agonist

A

activates receptor but not with maximal efficacy

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14
Q

inverse agonist

A

inactivates constitutively active receptor

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15
Q

maximum effect

A

further inc. in drug dose will not cause inc. response -> receptor is said to be saturated

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16
Q

Therapeutic index

A

TI=LD50/ED50
LD50: lethal dose for 50% of population
ED50: effective dose for 50% of population