Ch 2 terms (test 1) Flashcards

1
Q

Agonist

A

A drug that binds to and stimulated the activity of one or more receptors in the body

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2
Q

Antagonist, Inhibitor

A

A drug that binds to and inhibits the activity of one or more receptors in the body.

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3
Q

Bioavailability

A

A measure of the extent of drug absorption for a given drug and rout (%).

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4
Q

chemical name

A

the name that describes the chemical composition and molecular structure of a drug.

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5
Q

Cytochrome P-450

A

The general name for a large class of enzymes that play a significant role in drug metabolism.

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6
Q

Dependence

A

A state in which there is a compulsive or chronic need for the drug.

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7
Q

Drug

A

any CHEMICAL that affects the physiologic process of a living organism

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8
Q

First-pass effect

A

the initial metabolism in the liver of a drug absorbed from the gastrointestinal tract before the drug reaches systemic circulation through the bloodstream.

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9
Q

generic name, nonproprietary name

A

the name given to a drug by the united states adopted names council. (no trademark)

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10
Q

Half-life

A

in pharmacokinetics, the time required for half of an administered dose of drug to be eliminated by the body, or the time it takes for the blood level of a drug to be reduced by 50%.

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11
Q

Onset of action

A

the time required for a drug to elicit a therapeutic response after dosing.

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12
Q

Peak effect

A

the time required for a drug to reach its maximum therapeutic response in the body.

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13
Q

Peak level

A

the maximum concentration of a drug in the body after administration, usually measured in a blood sample for therapeutic drug monitoring.

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14
Q

Pharmacodynamics (2)

A

The study of the biochemical and physiologic interactions of drugs at their sites of activity. It examines the physicochemical properties of drugs and their pharmacologic interactions with body receptors.

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15
Q

Pharmacognosy (4)

A

The study of drugs that are obtained from natural plant and animal sources.

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16
Q

Pharmacokinetics (1)

A

The rate of drug distribution among various body compartments after a drug has entered the body. It includes the phases of absorption, distribution, metabolism, and excretion of drugs.

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17
Q

Pharmacotherapeutics (3)

A

The treatment of pathologic conditions through the use of drugs.

18
Q

Receptor

A

A molecular structure within or on the outer surface of a cell. Receptors bind SPECIFIC substances, and one or more corresponding cellular effect occurs as a result of this drug-receptor interaction.

19
Q

Steady state

A

The physiologic state in which the amount of drug removed via elimination is equal to the amount of drug absorbed with each dose.

20
Q

Therapeutic effect

A

The desired or intended effect of a particular medication.

21
Q

Tolerance

A

Reduced response to a drug after PROLONGED use (not addiction).

22
Q

Toxicology (5)

A

The study of poisons, including toxic drug effects, and applicable treatments

23
Q

Trade name, Proprietary name

A

The commercial name given to a drug product by its manufacturer.

24
Q

Trough level

A

The lowest concentration of drug reached in the body afar it falls from its peak level, usually measured in a blood sample for therapeutic drug monitoring.

25
Q

Absorption

A

process from entering human body until it is in the blood stream

26
Q

bioavailability

A

measures the amount of drug that has absorbed into the circulation.

27
Q

injection absorption rates

A

fastest:Intravenous (bypasses absorption for an immediate response)
Intramuscular: greater w/clear sol and in deltoid
Subcutaneous: massaging increases abs
Slowest: Intradermal

28
Q

factors affecting abs

A
  1. stomach dissolve (right side)
  2. stomach contents ( fat slows)
  3. sm intestine content
  4. exercise
  5. Pain
  6. motility
29
Q

oral formulation absorption

Fastest and slowest

A

FASTEST
sublingual; 3 min
SLOWEST
Enteric coating: dissolves in basic pH of LOWER small intestine. Contains caustic meds that could cause damage to stomach.

30
Q

Distribution

A

way in which drugs that have been absorbed are TRANSPORTED by body fluids to their site of action (target) organ. dependent on plasma proteins that carry the drug.

31
Q

metabolism, biotransformation

A

the way in which drugs are inactivated by the body into an inactive metabolite (water sol). LIVER

32
Q

Excretion

A

the elimination of a drug from the body. KIDNEY (biliary and lungs)

33
Q

duration of action

A

length of time that drug concentration is sufficient in the blood to produce a therapeutic response

34
Q

enzyme interaction

A

drug interacts with enzyme and inhibits action

35
Q

non selective interactions

A

alters cell membrane or the metabolic processes of the cell KILL CELL

36
Q

adverse drug reaction

A

any unexpected, unintended, undesired, or excessive response to a medication given at therapeutic dosages.

37
Q

teratogen

A

drug that causes birth deformity in unborn fetus

38
Q

incompatibility

A

2 parenteral drugs react when mixed resulting in deterioration of at least one.

39
Q

Intraarticular

A

within a joint

40
Q

Intrathecal

A

within a sheath (spinal chord)