definitions Flashcards

1
Q

Pharmacodynamics

A

mechanism of action of a drug on an organism

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

Pharmacokinetics

A

the process by which a drug is absorbed, distributed, metabolized (biotransformed) and eliminated by the body.

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

drug

A

a chemical agent that is used in the diagnosis, the treatment or the prevention of a disease.

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

Enteral routes

A

PO
SL
PR
gastric access via tube

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

Parenteral routes

A
IV
IM
SQ
Sl
drug depots
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Drug metabolism

A

GI–> portal circulation–Liver first

Kidneys cannot filter lipid soluble drugs–agents reabsorbed back into systemic circulaiton

A charged molecule cannot easily diffuse out of the kidney lumen and therefore a charged drug molecule is returned into the systemic circulation.

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

phase 1 liver metbolism of drugs

A

convert lipid soluble molecules into water soluble molecules by introducing or unmasking a polar group such as –OH or –NH2.

a drug bound to cytochrome P450 can be oxidized or reduced via NADPH

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Phase 2 liver drug metabolism

A

conjugation, wherein an endogenous polar group is added to a drug molecule—glucuronic acid, sulfuric acid, acetic acid or an amino acid.

This makes the molecule POLAR so kidney can excrete it

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

Bioavailability

A

the fraction of administered drug that reaches the systemic circulation in an unchanged form.

influenced by:
Solubility of the agent
Hepatic metabolism of the agent
Chemical binders

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Half life

A

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

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

loading dose

A

an initial dose of drug that is higher then subsequent doses for the purpose of rapidly achieving therapeutic drug concentrations in the serum.

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Potency

A

the amount of drug required to produce 50% of the maximal response that the drug is capable of inducing. Potency is a term more frequently used to compare drugs of a similar class.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

EC50

A

Effective Concentration in 50% of subjects tested

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

LD50

A

Lethal Dose in 50% of subjects tested

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Therapeutic index (T.I.)

A

a ratio of the dose of a drug that produces toxicity relative to the dose of the same drug that produces a clinically desired response.
T.I. = LD50 / EC50

17
Q

Physiologic antagonism

A

refers to two agonists in unrelated reactions which cause opposite effects.

18
Q

Neutralization antagonism

A

refers to a process in which two drugs bind to one another which serves to inactivate or partial inactivate each of the drugs.

19
Q

FDA/ DEA classification

A
CI – No approved medical use
 CII – High potential for abuse
 CIII – Moderate potential for abuse 
CIV – Low potential for abuse
OTC – Available over the counter