drug interactions Flashcards

1
Q

what is a drug interaction defined as?

A

the modification of a drugs effect by prior or concomitant administration of another drug

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2
Q

when has a drug interaction occurred?

A

when the pharmacological effect of two or more drugs given together is not just a direct function of their individual effects

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3
Q

what are the drugs that are most commonly involved in drug interactions?

A
lithium
digoxin
warfarin
theophylline
cyclosporin
phenytoin
gentamicin
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4
Q

what increases the chance of a drug-drug interaction occurring?

A
higher number of medications
being very old or young
critically ill patients
patients undergoing complicated surgical procedures
patients with chronic conditions
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5
Q

what are the 3 mechanisms by which drug-drug interactions may occur?

A

pharmaceutical
pharmacokinetic
pharmacodynamic

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6
Q

what are some examples of pharmacodynamic interactions?

A

antagonistic interactions
additive or synergistic interactions
interactions due to changes in drug transport
interactions due to fluid and electrolyte disturbances
indirect pharmacodynamic interactions

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7
Q

what can happen in the GI tract with regards to absorption of drugs?

A

interactions can occur that change the rate of absorption rather than the extent ( mostly) clinically significant when drugs have short half lives or high plasma levels are required rapidly

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8
Q

what happens in the GI tract with regards to drug binding?

A

drugs can bind to each other (such as tetracyline and erythromycin complex with iron, calcium and magnesium)

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9
Q

why is pH significant in determining the absorption rate of a drug?

A

absorption is affected by the degree of ionisation which is dependent on pH

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10
Q

what can reduce pH?

A

H2 agonists, proton pump blockers and antacids

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11
Q

what is the effect of broad spectrum antibiotics on normal gut flora?

A

destroys normal gut flora - can lead to OCP failure or digoxin toxicity

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12
Q

where are most oral medicines absorbed?

A

small intestine

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13
Q

what is the rate limiting step of absorption of oral medicines?

A

gastric emptying

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14
Q

when does protein binding displacement occur?

A

when there is a reduction in the extent of plasma protein binding of a drug caused by the presence of another drug

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15
Q

what does displacement of a drug from plasma proteins result in/

A

increased bioavailability of the displaced drug

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16
Q

what are the two most important plasma proteins with regard to drug binding?

A

albumin

alpha 1 glycoprotein

17
Q

when do drug interactions involving metabolism occur?

A

when one drug induces or inhibits the metabolism of another

18
Q

where does metabolism occur?

A

commonly in the liver via the cytochrome p450 system

19
Q

what drugs can inhibit the cytochrome system?

A
clarithromycin
erythromycin
omeprazole
CCBs
these drugs inhibit the metabolism of a small group of drugs metabolised by the cytochrome P450  system
20
Q

what drugs can induce cytochrome P450?

A

barbiturates
phenytoin - warfarin, steroids
rifampicin - warfarin
tobacco

21
Q

where does drug elimination occur?

A

the kidney

22
Q

what can inhibit drug excretion?

A

vrapamil/diltiazem

23
Q

what are the effects of loop diuretics?

A

increase tubular reabsorption

24
Q

what can beta blockers interact with?

A

agonists such as salbutamol

25
Q

what are synergistic interactions?

A

when two drugs with the same pharmacological effect are given concurrently

26
Q

what do NSAIDs interact with?

A

antihypertensive medication and heart failure treatment