dose relationship Flashcards

1
Q

What is a graded dose?

A

Response relationships depict the effect of varying doses of a drug on an individual

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

What is a normal distribution?

A

A “normal” distribution is also known as a bell-shaped curve or Gaussian curve. In a Gaussian or normal distribution, the mean , mode and median would all have the same (or similar) value and would look like the figure. Example would be body height, heart rate, blood pressure ect in a population.

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

What distribution does a drug response in a population usually show? why?

A

normal. because of individual variability, the response to a drug is not uniform in different subjects.

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

What is a quantal dose-response curve?

A

shows the average dose-releated effects of a drug in population of individuals. examples: survived vs non survived, sleep vs no sleep

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

What is therapeutic index?

A

it shows how selective the drug is in producing its therapeutic effects versus its adverse effects

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

What does a larger therapeutic index mean?

A

means greater margin of safety of a drug. Drugs with a small TI require frequent monitoring.

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

how to find Certain safety factor

A

LD1/ED99

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

what is the therapeutic window?

A

the range of drug concentration that provides therapeutic effects but with minimal toxic effects.

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

Advantages of Enteral route

A

Simple, inexpensive, convient, painless no infection

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

Disadvantages of Enteral route

A

Requires GI absorption. Slow delivery to site of pharmacologic action

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

Advantages of parenteral route

A

Rapid delivery to site of pharmacologic action. High bioavailability

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

Disadvantages of parental route

A

irreversible, infection, pain, fear, skilled personnel required.

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

Advantages of mucous membrane route

A

-rapid delivery to site of pharmacologic action, -often painless, -simple, -convenient , -low infection, -direct delivery to affected tissues possible

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

Disadvantages of mucous membrane route

A

few drugs have chemical characteristics or formulations that allow them to be administered via this route

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

Advantages of transdermal route

A

-simple -convenient -painless -excellent for continuous or prolonged administration

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

disadvantages of transdermal route

A

-requires highly lipophilic drug -slow delivery to the site of pharmacologic action -may be irritating

17
Q

What is the absorption pattern of IV route

A

-rapid onset -suitable for large volumes and for complex mixtures when diluted

18
Q

What is the special utility of IV route?

A

-valuable for emergency use -permits dosage titration and controlled drug delivery -usually required for protein and peptide drugs

19
Q

What are the limitation and precautions of IV route?

A

-increased risk of adverse effects -must inject slowly as a rule -not suitable for oily solution or poorly soluble substances

20
Q

What is the absorption pattern for Subcutaneous route?

A

slow onset

21
Q

What is special utility for subcutaneous route?

A

may be used for some poorly soluble suspensions, or slow-releasing implants

22
Q

What are the limitations and precautions for subcutaneous route?

A

-Small volumes -possible pain or necrosis from irritating chemicals

23
Q

What is the absorption pattern of IM route?

A

immediate onset

24
Q

What is the special utility of IM route?

A

suitable foe moderate volumes including oil based drugs

25
Q

what are the limitations or precautions for IM route?

A

-Can affect lab test (eg creatine kinase) -IM hemorrhage -painful

26
Q

What is the absorption pattern for PO route?

A

variable, depends on many factors

27
Q

What is the special utility for PO route?

A

-most convenient and economical -usually safer

28
Q

What are some of the limitation and precautions for PO route?

A

-requires patient compliance -bioavailability potentially erratic and incomplete

29
Q

What is the distribution phase after giving an IV?

A

immediately after IV administration of a drug, it rapidly distributes from “blood” (the vascular compartment) to “extravascular volume” in other body parts. The plasma concentration shows a steep decline.

30
Q

What is the elimination phase after giving an IV?

A

when the drug concentration decreases slowly following its metabolism and excretion

31
Q

What is the first pass effect?

A

Following intestinal absorption, the portal blood delivers the drug to the liver, which is responsible for most of the biotransformation (metabolism) before drugs entering the systemic circulation

32
Q

What route does the first pass effect impact?

A

only orally administered drugs

33
Q

What may happen to some drugs by the first pass effect?

A

Some drugs may be extensively metabolized and inactivated by the liver, whereas other drugs may be converted into active compounds

34
Q

What does the fraction of administered drug that reaches the systemic circulation depend on?

A

-route of administration -drugs chemical form -Patient variabilities (enzymes, and transporter proteins in GI track and liver)

35
Q

How to you find bioavailability?

A

F=(quantity of drug reaching systemic circulation)/ (quantity of drug administered)

36
Q

what is the rising phase?

A

drug continues to be absorbed and distributed until the drug concentration (Cp) reaches a peak. Drug effects intensify.

37
Q

What is the decaying phase?

A

drug elimination becomes more dominant. effect disappears when Cp falls below drugs therapeutic level