Pharmacodynamics, Drug Interaction And Toxcity Flashcards

(22 cards)

1
Q

What are the advantages of drug selectivity?

A

The more selective a drug is, the lesser the chance it will interact with different receptors and therefore the lesser chance of undesirable effects

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2
Q

What does drug specficity mean?

A

Targeting a receptor subtype that allows the treatments to be targeted to a particular organ

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3
Q

What is the efficacy of a drug?

A

The ability of a drug to produce a response

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4
Q

What is a drugs potency?

A

The dose required to poduce the desired biological response

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5
Q

Describe agonist potency?

A

Defined by the drug concentration at which 50% of the maximal response is obtained

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6
Q

Describe antagonist potency?

A

the concentration that reduces the maximal reaction bu 50%

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7
Q

How is potency affected by competitive antagonism?

A

Agonist efficacy can be restored by increasing the agonist, and so the EC50 changes but the maximal effect stays the same

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8
Q

What is the thearpeutic index

A

The relationship between the concetration causing adverse effects and the concentration causing the desired effects

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9
Q

What is the therapeutic window?

A

The range of doses that can effectively treat a condition whilst remaining safe

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10
Q

What are some of the different types of pharmaockientic drug drug interactions?

A

Absorbtion, metabolism and hepatic effects, drug food interactions

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11
Q

What are some of the ways that drug drug interactions can effect absorption?

A

Changes in gut motility

Changes in volume of distrubtion.

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12
Q

How can drugs effect the gut motlitly and therefore absorption of other drugs?

A

Opiates and atrophine slow the gut which decreases the absorbtion of drugs, whereas meloclomprimide increases the speed of the gut and therefore increases absorption of drugs

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13
Q

How can drugs effect the volume of distrubtion of other drugs?

A

Interactions between drugs affecting the protein binding of different drugs

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14
Q

What are some of the ways that drugs can have metabolism or hepatic effects on other drugs?

A

Drugs can be inhibitors or inducers of cyp 450 enzymes
Inhibition causes decreased metabolism of drugs and possible ADR whereas induction causes increased metabolism of drugs and therefore a reduction in effect

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15
Q

Give an example of how drugs and food can interact?

A

Grapefruit juice can inhibit cYP450 enzymes and therefore cause decreased metabolism of a drug

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16
Q

Name some drugs that are CYP450 inducers

A

Phenytonin, Carbamazepine, Alchol, Rifampicin, Barbiutates and sulphonureas

17
Q

Name some drugs that are CYP450 inhibitors?

A

Omeprazole, disulfram, erythromycin, valporate, isonzid, ciemtadine and ciprofloxin, ethanol and suplonamides

18
Q

What are some of the classes of drug that commonly cause drug durg interactions?

A

Antibiotics such as rifampicin and quionlones
Anticonvuslants such as carbamazepine and phenytonin
Anticogulants such as warafrin
Antiarrythmics such as amidarone
Antidepressants

19
Q

How can renal disease interact with drugs?

A

Causes a falling gfr which results in reduced clearnace, and can cause a disturbamce of electrolytes that predisposes to toxicity, and then nephrotoxins can futher disrput kidney function

20
Q

How can hepatic disease interact with drugs?

A

Reduced clearnace of hepactically metabolised drugs, reduced cyp450 activity and longer half lives, and can cause hypoalbuminea reducing the binding of drugs and therefore leading to an increased excretion

21
Q

How can cardaic disease interact with drugs?

A

Falling cardiovascular output can lead to a excessive response ot hypotensive agents, can caused reduced organ perfusion and therefore reduced perfusion of the liver and kidneys

22
Q

How can drug drug interactions result from excretion?

A

Can cause changes in tubular flow ph, as well as changes in protein binding, for example NSAIDs inhbit tubluar secretion and therefore cause increased levels of a drug