Final definitions Flashcards

1
Q

drug

A

a chemical agent used in the dx, tx or prevention of disease

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2
Q

Drug routes

A

enteral, parenteral, inhalation, intranasal, intrathecal, topical, transdermal, sublingual, and IV

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3
Q

What’s unique about sublingual route?

A

drug delivered to blood stream, skips first pass by liver

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4
Q

What’s unique about IV route?

A

100% bioavailability

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5
Q

Drug absorption rule

A

small non-ionized, lipid soluble drugs will more readily cross plasma membrane relative to larger, ionized and/or water soluble molecules

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6
Q

bioavailability

A

is the fraction of administered drug that reaches the systemic circulation in an unchanged form. Solubility of agent, hepatic metabolism of agent, and chemical binders influence bioavailability.

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7
Q

Half life

A

is the amount of time required for the plasma concentration of a drug to decrease by 50% after discontinuation of the drug.

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8
Q

loading dose

A

initial dose of drug that is higher than subsequent doses for purpose of achieving therapeutic drug concentration.

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9
Q

maintenance dose

A

dose of a drug that maintains a steady state plasma concentration in therapeutic range.

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10
Q

onset

A

amount of time it take for a drug to exert effects

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11
Q

Duration

A

the length of time for which a drug exerts therapeutic effects.

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12
Q

Efficacy

A

refers to the degree to which a drug is able to induce maximal therapeutic effects. Efficacy is a term often used to compare drugs of different classes.

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13
Q

Potency

A

is the amount of drug required to produce 50% of the maximal response that the drug is capable of producing. Potency is more frequently used to compare drugs of similar classes.

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14
Q

EC50

A

: effective concentration 50 is the concentration of an agent which induces a specific clinical effect in 50% of subject to which drug has been administered.

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15
Q

LD50

A

lethal dose 50 is the concentration of an agent which causes death in 50% of subject to which that agent has been administered.

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16
Q

Therapeutic index: (TI)

A

(TI) = LD50/EC50. - A measure of drug’s safety. Large number is good, small number is bad.

17
Q

Agonist

A

an agent that can bind to a receptor site and elicit a defined therapeutic response

18
Q

partial agonist

A

occupies a binding site but causes less of response than a full agonist

19
Q

antagonist

A

inhibit or block response caused by agonist

20
Q

competitive antagonist

A

interact with receptors at the same site as agonist and thus compete for binding.

21
Q

non-competitive antagonist

A

bind to a site other than the agonist. (effects are generally irreversible)

22
Q

tolerance

A

a decreased response to a drug. Clinically dose of drug must be increased to achieve a similar effect of the drug at its original dose.

23
Q

supplement

A

intended to “supplement the diet”, contains vitamins, minerals, herbs or botanicals, or a concentrate/metabolite/constituent or combo of these things.

  • May not claim to treat, diagnose, cure or prevent disease
  • Can make “structure or function claims”….. can support joints…etc.
24
Q

pregnancy Rx classification

A
  • A: controlled studies show no risk
  • B: no evidence of risk in humans
  • C: risk cannot be ruled out
  • D: positive evidence of human fetal risk
  • X: contraindicated in pregnancy
    o Most drugs are category C— so contraindicated w/ pregnancy.
25
Q

FDA/DEA classification Rx

A

CI: no approved medical use (LSD, heroine)
CII: high potential for abuse, increased rate of addiction, need a new script to refil.
CIII: moderate potential for abuse
CIV: low potential for abuse (lowest dose of codeine)
OTC: available over the counter.