pharmodynamics Flashcards

1
Q

what type of reaction is within an above therapeutic range and give an example of the reaction

A

toxic reaction

example: bleeding following too high dose of anticoagulant

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2
Q

what type of reaction is within a therapeutic range and give an example of the reaction

A

collateral

example: drowsiness with antidepressant

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3
Q

what type of reaction is within a below therapeutic range and give an example of the reaction

A

hyper susceptibility reaction

example: penicillin reaction

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4
Q

What are first dose reactions and give an example

A

Occur straight away. hypotension after first dose of ACE inhibitor

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5
Q

give an example of the reaction of early reactions

A

nitrate-induced headache

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6
Q

What are intermediate reactions and give an example

A

Happen within days to weeks of taking the drug. thromboembolism due to antipsychotic drugs

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7
Q

What are late reactions give an example

A

bruising due to corticocosteroids

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8
Q

When do withdrawal reactions occur.

give an example of the reaction of withdrawal reactions

A

After the medication is stopped

SSRI antidepressant discontinuation

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9
Q

What are delayed reactions

give an example of the reaction of delayed reactions

A

Side effects that appear long after stopped. severe white blood cell loss after certain chemotherapy drugs

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10
Q

what are the four types of pharmocological actions of drugs

A
  1. via direct effects on cellular receptor function
    2 via action on ion Channels
  2. Via action on membrane transport processes
  3. via enzyme inhibition
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11
Q

what is an agonist

A

molecule that binds to a receptor and activates it

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12
Q

what is a partial agonist

A

an agonist that cannot illicit the same change as a full agnostic

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13
Q

what are antagonists

A

diminish or abolish the effect of an agonist via interaction with the receptor

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14
Q

what are the two types of antagonists

A

competitive and non-competitive

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15
Q

what are competitive antagonists

A

compete for the same binding site as the agonist

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16
Q

what are non-competitive antagonists

A

alter the binding ‘site’ for the agonist, which decreases agonist activity

17
Q

drugs that act on ion channels commonly affect…

what is an example of a drug

A

neural transmission and muscle contractibility and vaerapamil

18
Q

what is the function of transporters, what is a drug that affects the function

A

mediate the movement of specific endogenous molecules and nutrients in and out of the cell

Sertraline

19
Q

what are phrarmodynamic interactions

A

interactions between drugs which have similar or antagonistic pharmacological or side effects

20
Q

what are pharmokinetic interactions

A

part of a key point in the metabolism PK phase where drugs can directly alter the activity of the liver

21
Q

which type of interaction are predictable

A

phrarmodynamic

22
Q

what are pharmacogenetics

A

variations can occur in individual response to a drug, if you don’t have the enzyme you can’t metabolise the drug

23
Q

pharmcogenetics is important for

A

personalised medicine

24
Q

what is polypharmacy

A

where people take > 4 medicines simultaneously

25
what is an adverse drug reaction
effect of a drug beyond its anticipated therapeutic effects occurring during clinical use
26
what are adverse drug reactions ADRs classified by
DoTS classification
27
what does DoTS classification stand for
Dose time-course susceptibility
28
below dose ADRs result in
permanent avoidance of the drug
29
within therapeutic range ADRs result in
may not be unavoidable, may not reduce by reducing dose
30
above therapeutic range ADRs result in
treat by reducing dose
31
what do ACE inhibitors effect
enzymes
32
example Cytochrome PY50 what happens when CYP50 is induced what happens during initiation of CYP50 what happens during withdrawal of CYP50
1. rate of metabolism of other drug increases, decreasing plasma concentration = decreased effect 2. rate of metabolism of other drug deceased, plasma concentration increases = toxicity 3. plasma concentration of other drug increases = decreased rate of metabolism of other drug = increased plasma concentration and increased toxicity
33
what are examples of drugs affected by PY50 induction/inhibition (remember the acronym COWPAT)
C ciclosporin O oral contraceptive pill W warparin P phenytoin A Ace inhibitors T theophylline S statins