Pharm2 Flashcards

1
Q

how do we measure drug clearance in body

A

half life (covalent bonds can affect, prolong this)

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2
Q

what type of bonding occurs between the beta blocker-receptor

A

ionic bond

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3
Q

A wide therapeutic index would indicate what:

A

a safe range to treat with little risk of harm

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4
Q

Can the same drug have different TI

A

yes, for example ppl take more ibuprofen for inflammation vs. pain so narrows the therapeutic index

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5
Q

Up-regulation

A

antagonist causes “weak” signal so more receptors

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6
Q

down regulation

A

from an agonist drug causing “stronger” signal, reduces receptors

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7
Q

tachyphylaxis

A

very fast tolerance build to drugs

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8
Q

atropine would be an agonist or antagonist to the parasympathetic

A

antagonist because it is anticholinergic

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9
Q

define titrate and taper in relation to dosing drugs

A

titrate-“start low and go slow”
Taper-wean them off
both help prevent risk of tolerance

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10
Q

It is important to use hyperreactivity/hyporeactivity to a drug vs. hypersensitivity (allergic rxn)

A

adverse drug reactions

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11
Q

the most common adverse drug reaction

A

digestive disturbances (esp. oral) and hypersensitivity

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12
Q

Type I hypersensitivity

A

immediate, IgE antibodies involved. requires a 1st exposure penicillin, food can cause anaphylaxis

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13
Q

Type IV Hypersensitivity

A

T cell mediated diseases, delayed onset, can occur at 1st exposure

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14
Q

what are the weakest bonds

A

hydrophobic (such as fat soluble substances that group together to avoids water, they are reversible

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15
Q

Where would you see a greater change in affect when giving a drug?

A

at lower concentrations…. the higher dose may see receptors saturated

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16
Q

what does a graded response graph show

A

the percentage of maximum response over time

17
Q

Explain the MEC of a graded response graph

A

the minimum effective concentration, (lowest dose to have an affect on a parameter aka symptom/pain/sign/etc.)

18
Q

the therapeutic window is between which two points on a graded response graph

A

the Minimum effective concentration for an adeverse response and the min.EC for a desired response

19
Q

define the Duration of Action

A

time range during which the drug concentration exceeds MEC for a desired response

20
Q

what calculation is used to determine therapeutic index/window

A

ratio between Letha Dose50 and EffectiveDose50

21
Q

when two drugs are compared by their potency’s which one will be more potent and therefore more effective on a graph

A

the one on left

22
Q

what does it mean if Drug X is on the left compared to drug Y on a potency graph

A

Drug x is more effective

23
Q

tyrosine kinase is an enzyme that does what:

A

transfers phosphate group from ATP to a protein. It functions as an “on-Off switch for cell functions like metabolism/differentiation

24
Q

which type of ligand-receptor is most seen with neurotransmitters

A

ion channels

25
Q

What example is a second messenger system?

A

G protein that increases concentration of cAMP, IP3 or Ca++

26
Q

Distinguish between an inverse drug and antagonist

A

inverse actually causes the opposite of the agonist response vs. antagonist just blocks the agonist

27
Q

mixed agonist/antagonist would elicit what type of response

A

some drugs that cause pain relief at one receptor and no effect at another (opiods)

28
Q

whats one example of a hormone signaling system?

A

tyrosine kinase (transfers phosphate to ATP; functions as on/off switch for metabolis or cell diffentiation

29
Q

beta-blockers and atropine are examples of agonist or antagonist?

A

antagonist