Pharm I - Fleckenstein Flashcards

1
Q

Define Pharmacokinetics

A

Actions the body has ON the drug

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2
Q

Define Pharmacodynamics

A

Actions the drugs has ON the body

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3
Q

Describe an Agonist

A

-A natural drug or Ligand -Activates receptor

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4
Q

This is usually competes with the agonist with the binding site but does not activate the receptor

A

Antagonist (competitive inhibitor)

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5
Q

In what direction does the antagonist usually shift the dose response curve?

A

To the right

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6
Q

Describe an allosteric inhibitor

A

Binds to different site than agonist and antagonist. NONCOMPETITIVE And creates conformational change to receptor as to agonist can no longer bind

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7
Q

What is a full agonist

A

High affinity for Ra. Ra-D complex favored, Larger effect observed

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8
Q

Partial agonist

A

Intermediate affinity for Ra and Ri. Ra-D not stabilized as well than in Full agonist

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9
Q

Inverse agonist

A

Higher affinity for Ri. DON’T confuse with Antagonist. Reduce constitutive activity

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10
Q

What is a conventional antagonist

A

Equal affinity for Ra and Ri NO CHANGE in constitutive activity

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11
Q

Which of the following drug receptor interaction has a net effect GREATER than the sum -Additive -Synergistic -Antagonistic

A

SYNGERSITIC (1+1 = 5) Additive - 1+1 = 2 Antagonistic 1+1 = 0.5

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12
Q

This antagonist does not involve a receptor, a good example is a protein disrupting pH counteracting the effects of the drug

A

Chemical antagonist

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13
Q

Define Efficacy

A

Number of receptos that must be activated to yeild max response

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14
Q

How is potency different than efficacy?

A

Efficacy refers to the number of receptors where as potency refers to the amount of the drug needed. So a POTENT drug would require little dosage to illicit a max response.

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15
Q

This is a measure of the drug’s ability to produce a change in cellular activity

A

Intrinsic activity

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16
Q

This is a measure of the Tightness that a drug BINDS to the receptor

A

Affinity

17
Q

Define Therapeutic index

A

TI = TD(50)/ED(50) You want a large Toxic does over a small effective dose

18
Q

Define margin of safety

A

T.D (1%) / E.D. (99%)

19
Q

What is the fastest mode of mode of dosage for drugs

A

Intravenous or (Parenteral)

20
Q

Oral or Rectal administration is an example of ………

A

Enteral (by way of intestine)

21
Q

What is a disadvantage of oral administration (enteral)

A

Most unpredictable

22
Q

Which line is the most potent

A

Line B