dose relationship Flashcards

(37 cards)

1
Q

What is a graded dose?

A

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

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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.

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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.

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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

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5
Q

What is therapeutic index?

A

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

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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.

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7
Q

how to find Certain safety factor

A

LD1/ED99

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8
Q

what is the therapeutic window?

A

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

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9
Q

Advantages of Enteral route

A

Simple, inexpensive, convient, painless no infection

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10
Q

Disadvantages of Enteral route

A

Requires GI absorption. Slow delivery to site of pharmacologic action

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11
Q

Advantages of parenteral route

A

Rapid delivery to site of pharmacologic action. High bioavailability

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12
Q

Disadvantages of parental route

A

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

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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

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14
Q

Disadvantages of mucous membrane route

A

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

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15
Q

Advantages of transdermal route

A

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

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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?

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
what are the limitations or precautions for IM route?
-Can affect lab test (eg creatine kinase) -IM hemorrhage -painful
26
What is the absorption pattern for PO route?
variable, depends on many factors
27
What is the special utility for PO route?
-most convenient and economical -usually safer
28
What are some of the limitation and precautions for PO route?
-requires patient compliance -bioavailability potentially erratic and incomplete
29
What is the distribution phase after giving an IV?
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
What is the elimination phase after giving an IV?
when the drug concentration decreases slowly following its metabolism and excretion
31
What is the first pass effect?
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
What route does the first pass effect impact?
only orally administered drugs
33
What may happen to some drugs by the first pass effect?
Some drugs may be extensively metabolized and inactivated by the liver, whereas other drugs may be converted into active compounds
34
What does the fraction of administered drug that reaches the systemic circulation depend on?
-route of administration -drugs chemical form -Patient variabilities (enzymes, and transporter proteins in GI track and liver)
35
How to you find bioavailability?
F=(quantity of drug reaching systemic circulation)/ (quantity of drug administered)
36
what is the rising phase?
drug continues to be absorbed and distributed until the drug concentration (Cp) reaches a peak. Drug effects intensify.
37
What is the decaying phase?
drug elimination becomes more dominant. effect disappears when Cp falls below drugs therapeutic level