Session 1 Flashcards

1
Q

How do you calculate steady state concentration in plasma?

A

CpSS = dose rate / clearance

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

How do you calculate loading dose?

A

Volume of distribution x CpSS

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

What is the difference between zero order and first order kinetics?

A

Zero (non-linear) = rate of elimination is constant. No half-life can be defined.

1st (linear) = rate of elimination is proportional to drug level. Constant fraction of drug is eliminated in unit time. Elimination becomes non-linear at higher levels.

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

What is clearance?

A

The volume of plasma that is completely cleared of the drug per unit time.

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

How do you calculate half life?

A

T1/2 = (0.693 x Vd)/clearance

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

Name CYP inhibitors

A
G- grapefruit juice
O- omeprazole
D- disulfiram
E- erythromycin
V- valproate
I- isoniazid
C- cimetidine/ciprofloxacin
E- ethanol
S- sulphonamides
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Name CYP inducers

A
P- phenytoin
C- carbamezepine
B- barbiturates
R- rifampicin
A- alcohol
S- sulphonylureas
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Describe phase 1 and phase 2 of drug metabolism

A
1 = oxidation/reduction/hydrolysis via CYP 450
2 = conjugation with glucoronyls/sulphates/methyls/acetyles etc.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

How do you calculate volume of distribution?

A

Total amount of drug in the body / plasma concentration of drug at time zero

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

What are the major fluid compartments of the body?

A

Plasma, extracellular and intracellular fluid.

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

What factors affect drug distribution?

A

Lipophilicity (moves from blood plasma to tissues)
Hydrophobicity
Plasma binding reduces entry into tissues.
Amount of tissue and density of binding sites within that tissue.

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

How do you calculate bioavailability?

A

Amount of drug reaching systemic circulation / total amount of drug given

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

How do you calculate oral bioavailability?

A

The amount getting in orally / Total amount administered via IV.

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

What are parenterally delivered drugs?

A

Do not involve the GI tract. E.g. IV, subcutaneous, transdermal, intramuscular and intrathecal.

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

What are black triangle drugs?

A

They are being intensively monitored.
Newly released, changed indications, changed formulations or combination products.
Yellow cards must be submitted for the drugs for all suspected reactions.

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