Ch.1 Flashcards

1
Q

Pharmaceutic

A

(dissolution) drug becomes a solution so that it can cross the biologic membrane.

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2
Q

Pharmacokinetic

A

the process of drug movement to achieve drug action. 4 processes: absorption, distribution,metabolism or (biotransformation), and excretion (or elimination).

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3
Q

Pharmacodynamic

A

A branch of pharmacology dealing with the reactions between drugs and living systems

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4
Q

Excipients

A

an inactive substance formulated alongside the active ingredient of a medication, for the purpose of bulking-up formulations that contain potent active ingredients.

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5
Q

Disintegration

A

the breakdown of a tablet into smaller particles.

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6
Q

Dissolution

A

is the dissolving of the smaller particles in the GI fluid before absorption.

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7
Q

Rate limiting

A

is the time it takes the drug to disintegrate and to dissolve to become available for the body to absorb it.

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8
Q

Passive absorption

A

occurs mostly by diffusion (movement from higher concentration to lower concentration) with diffusion the drug does not require energy to cross the membrane.

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9
Q

Active absorption

A

requires a carrier such as an enzyme or protein to move the drug against a concentration gradient. Energy is required.

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10
Q

Pinoytosis

A

is the process by which cells carry a drug across their membrane by engulfing the drug particles.

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11
Q

First pass effect

A

the process in which the drug passes to the liver first also know as (hepatic first pass) Ex, Morphine,warfarin.

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12
Q

Bioavailability

A

is a subcategory of absorption.

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13
Q

Distribution

A

the process by which the drug becomes available to body fluids and body tissues.

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14
Q

Drugs that are greater than 89% bound to protein

A

highly protein-bound drugs

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15
Q

Drugs that are 61- 89% bound to protein

A

Moderately high protein-bound

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16
Q

Drugs that are 30-60% bound to protein

A

moderately protein-bound

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17
Q

Drugs that are less than 30% bound to protein

A

low protein-bound

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18
Q

Free drugs

A

drugs not bound to protein. are active and can cause a pharmacologic response.

19
Q

Metabolism

A

primary site in liver.

20
Q

The half-life (t1/2)

A

of a drug is the time it takes for one half of the drug concentration to be eliminated.

21
Q

Elimination

A

main route of drug elimination is through the kidneys (urine)

22
Q

The most accurate test to determine renal function is?

A

Creatinine clearance (CLcr)

23
Q

Pharmacodynamics

A

is the study of drug concentration and its effects on the body.

24
Q

Onset of action

A

is the time it takes to reach minimum effective concentration (MEC) after a drug is administered.

25
Q

Peak action

A

occurs when the drug reaches its highest blood or plasma concentration.

26
Q

Duration of action

A

is the length of time the drug has a pharmacologic effect.

27
Q

A time responsive curve

A

evaluates three drug parameters

28
Q

There are 4 receptor families

A
  1. kinase-linked receptors
  2. ligand-gated ion channels
  3. G protein-coupled receptor systems
  4. Nuclear receptors
29
Q

Agonists

A

drugs that produce a response

30
Q

antagonists

A

drugs that block a response

31
Q

Nonselective drugs

A

drugs that affect various receptors.

32
Q

The therapeutic index

A

estimates the margin of safety of a drug through the use of a ratio that measures the effective (therapeutic or concentration) dose (ed) in 50% of persons or animals (LD50)

33
Q

Low therapeutic index

A

have a narrow margin of safety.

34
Q

High therapeutic index

A

have a wide margin of safety and less danger of producing toxic effects.

35
Q

Peak drug level

A

is the highest plasma concentration of drug at a specific time.

36
Q

Trough drug level

A

is the lowest plasma concentration of a drug, and it measures the rate at which the drug is eliminated.

37
Q

Loading dose

A

when immediate drug response is desired, a large initial dose, of drug is given to achieve a rapid minimum effective concentration in the plasma.

38
Q

Side effects

A

are physiologic effects not related to desired drug effects.

39
Q

Adverse reactions

A

are more severe than side effects

40
Q

Toxic effects or toxicity

A

of a drug can be identified by monitoring the plasma (serum) therapeutic range of the drug.

41
Q

Pharmacogenetics

A

is the scientific discipline studying how the effect of a drug action varies from a predicted drug response because of genetic factors or hereditary influence.

42
Q

Tolerance

A

refers to a decreased responsiveness over the course of therapy.

43
Q

tachyphylaxis

A

refers to rapid decrease in response to the drug.

44
Q

A placebo effect

A

is a psychological benefit from a compound that may not have chemical structure of a drug effect.