chapter 4 part 2 Flashcards

1
Q

Indirect interactions

A

Drug A alters the endogenous levels and affects Drug B

  1. diuretics decrease K+ plasma conc, and enhance digoxin and glycoside toxicity.

2.MAO I- inhibit metabolism of Ne AND SO Ne WILL INCREASE in levels, tyramine and ephedrine

  1. H-1 receptors antagonists mepyramine, which causes drowsiness and if taken with alcohol can lead to accidents
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2
Q

Age on drug response :

A

Drug responses can vary due to: DIMINISHED CARDIAC OUTPUT (heart attack)

  • diminish hepatic metabolism
    -can prolong the duration of the drug action

-Increasing body fat will increase Vd levels, and decrease plasma protein binding. this promotes the accumulation of highly lipid-soluble agents : diazepam (valium) and thiopental (pentothal).

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3
Q

age

A

neonates immature organs: reduced hepatic metabolism and renal excretion

elders: difference in Vd, renal clearance, absorption, hepatic metabolism

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4
Q

CYP3A4 (inhibitor)

A

Grapefruit juice are potent inhibitors of this in the intestine wall of mucosa

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5
Q

CYP1A2(inducer)

A

VEGETABLES LIKE brussel sprouts, cabbage, califlower and hydropcarbons in broiled meat

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6
Q

tetracyclines and fluoroquinolone antibiotics

A

calcium in dairy products can chelate these drugs

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7
Q

cigarette smokers have rapid metabolism compared to nonsmokers

A

b/c of enzyme inducer CYP1A

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8
Q

industrial workers exposed to pesticides will

A

metabolize certain drugs rapidly

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9
Q

drug-drug interactions

A

at the same time, one drug will affect and produce a pharmacological response

pharmacokinetics and pharmadynamic interactions

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10
Q

pharmadynamic interactions

A

direct interaction - drug A blocks drug b target site and diminishes or antagonizes drug b effect

ex; B-adrenoreceptors antagonists diminishes B-receptor agonists (propranolol salbutamol and terbutaline)

indirect interactions - drug A alters the endogenous levels of actions of Drug B

ex. diuretics will decrease k concentrations and enhance glycoside toxicity and digoxin

ex. MAO inhibitors will inhibit NE metabolism and increase NE levels like ephedrine and tyramine

ex. H-1 receptors antagonists like mepyramine cause drowsiness and when mixed with alcohol leads to accidents

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11
Q

pharmacokinetic interactions-clinically relevant

A

drug response cure is STEEP
therapeutic range is NARROW

EX. anti convulsions, antiarrhythmics, antithrombotics, antineoplastics, immunosuppressants, lithium

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12
Q

in vitro drug interactions

A

one drug interacts in vitro with another drug can inactive one or both drug

ex. thiopentone and suxamethonium - not in the same syringe but a complex is formed

ex. heparin is highly charged and interacts with basic drugs like this

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13
Q

absorption

A

gi absorption is slowed when drug inhibits emptying of gastric (Atropine and opiates)

gi absorption is accelerated by drugs like metoclopramide

calcium and iron with tetracycline will cause an insoluble complex which decreases absorption

cholestyramine is a bile acid binding resin used to treat hypercholesteremia and binds with warfarin and dioxin to prevent absorptions

epinephrine and anesthetic causes vasoconstriction and slows the anesthetic absportions

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14
Q

distributions

A

displacement of drug from binding site and increase conc of free drug

then an increase excretion produces a new steady state of drug conc in plasma is decrease but free drug conc is the same as before displacing drug

toxicity from displacement can occur BEFORE NEW steady state

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15
Q

displacing agents

A

aspirin and sulfonamides like hydrate choral because of tight/strong binding to plasma albumin

ex aspirin displaces warfarin and valproate

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16
Q

metbolism

A

inducer and subsrate = increase clearance

inhibitor and substrate= decrease clearance

17
Q

inducer that enhances mebotlism

A

st johns wort ritonavir and rifapim

18
Q

inhibotors that inhibit metbolism

A

itraconazole and grapefruit juice

19
Q

rate of renal excretion is affected by

A

inhibiting the tubular secretion
altering urine flow and urine ph
altering plasma protein binding and filtration

20
Q

example of inhibition of tubular secretion

A

probenecid inhibits penicillin secretions so prolong action and also inhibits AZT

21
Q

alteration of urine flow and pH

A

loop and thiazide diuretics increase Li reabsorption, so li toxicity occurs when there is li carbonate for mood disorders

Urine pH- helps to detect the treatment for poisoning not cause of interactions