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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Antagonist, Inhibitor

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Bioavailability

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

chemical name

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Cytochrome P-450

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Dependence

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Drug

A

any CHEMICAL that affects the physiologic process of a living organism

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

generic name, nonproprietary name

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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%.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Onset of action

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Peak effect

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Pharmacognosy (4)

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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
Absorption
process from entering human body until it is in the blood stream
26
bioavailability
measures the amount of drug that has absorbed into the circulation.
27
injection absorption rates
fastest:Intravenous (bypasses absorption for an immediate response) Intramuscular: greater w/clear sol and in deltoid Subcutaneous: massaging increases abs Slowest: Intradermal
28
factors affecting abs
1. stomach dissolve (right side) 2. stomach contents ( fat slows) 3. sm intestine content 4. exercise 5. Pain 6. motility
29
oral formulation absorption | Fastest and slowest
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
Distribution
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
metabolism, biotransformation
the way in which drugs are inactivated by the body into an inactive metabolite (water sol). LIVER
32
Excretion
the elimination of a drug from the body. KIDNEY (biliary and lungs)
33
duration of action
length of time that drug concentration is sufficient in the blood to produce a therapeutic response
34
enzyme interaction
drug interacts with enzyme and inhibits action
35
non selective interactions
alters cell membrane or the metabolic processes of the cell KILL CELL
36
adverse drug reaction
any unexpected, unintended, undesired, or excessive response to a medication given at therapeutic dosages.
37
teratogen
drug that causes birth deformity in unborn fetus
38
incompatibility
2 parenteral drugs react when mixed resulting in deterioration of at least one.
39
Intraarticular
within a joint
40
Intrathecal
within a sheath (spinal chord)