drug interactions Flashcards

1
Q

when does a drug interaction occur?

A

occurs when a substance alters the expected performance of a drug

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2
Q

what are the two types of drug interactions?

A
  1. Pharmacodynamic
  2. Pharmacokinetic
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3
Q

when do pharmodynamic interactions occur?

A

Occur when drugs have an effect on the same target or physiological system

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4
Q

when do pharm-kinetic reactions occur?

A

Occur when a drug affects the pharmacokinetics (absorption, distribution, metabolism or excretion) of another drug

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5
Q

describe pharmacodynamic interactions

A

Pharmacodynamic interactions are either synergistic or antagonistic
Due to drugs acting on the same drug receptor(s) or physiological system
Generally predictable (related to pharmacology of drug)
Highly selective drugs are less likely to be problematic

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6
Q

Pharmacodynamic interactions (drug receptors)
Synergistic interaction

A
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7
Q

Pharmacodynamic interactions (drug receptors)
Antagonistic interaction

A
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8
Q

Pharmacodynamic drug reactions (physiological system)
Synergistic interaction

A
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9
Q

Pharmacodynamic drug reactions (physiological system)
Synergistic interaction

A
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10
Q

Pharmacodynamic drug reactions (physiological system)
Synergistic interaction

A
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11
Q

define synergy

A

interaction of drugs such that the total effect is greater than the sum of the individual effects (1+1>2)

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12
Q

define antagonism

A

an antagonist is a substance that acts against and blocks an action (2 drugs opposed to each other) (1+1=0)

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13
Q

define summation

A

different drugs used together to have the same effect as a single drug would (1+1=1)

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14
Q

define potentiation

A

enhancement of one drug by another so that the combined effect is greater than the sum of each one alone (1+1=1+1.5)

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15
Q

define pharmacodynamics

A

the effect the drug has on the human body

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16
Q

define pharmacokinetics

A

what the body does with the drug (the disposition of a compound within an organism)

17
Q

risk factors f

A

Narrow therapeutic index
Steep dose/response curve
Saturable metabolism

18
Q

what are the pharmacokinetics mechanisms?

A

Absorption, Distribution, Metabolism, Excretion

19
Q

describe Absorption in ADME

A

Motility – if the gut has slowed digestion, the drugs won’t work as well (oral contraceptive pill and antibiotics is the most common interaction)
Acidity – pH and pKa interactions.
Solubility
Complex formation

20
Q

Describe distribution in ADME

A

Drugs can go into the proteins, other tissues or the effect site
Protein binding

21
Q

How is protein binding helpful in drug distribution?

A

If you give 2 highly protein bound drugs, they will make each other strong and increase their effect so you always make sure you know what drugs the patient has taken before giving them new drugs

22
Q

describe metabolism in ADME

A

CYP450
INHIBITION
INDUCTION
EXCRETION

23
Q

describe CYP450 in metabolism

A

Haemoproteins
Metabolise many substrates – endogenous and exogenous

24
Q

describe inhibition in metabolism

A

Drug A blocks metabolism of drug B, leaving more free drug B in the plasma so it has an increased effect

25
Q

describe induction in metabolism

A

Drug C induced CYP450 isoenzyme leading to increased metabolism of drug D so it has a decreased effect

26
Q

two types of excretion in metabolism

A

renal
billary - minor

27
Q

describe renal exertion in metabolism

A

pH dependant
Weak bases – cleared faster if urine acidic
Weak acids – cleared faster if urine alkali

28
Q

what are the different types of pharmacodynamic mechanisms

A

receptor based
signal transduction
physiological systems

29
Q

describe receptor based pharmacodynamic mechanisms

A

Agonists
Partial agonists
Antagonists
Competitive
Non-competitive

30
Q

describe physiological systems in pharmacodynamic mechanisms

A

Different drugs that effect different receptors, but in the same physiological system

31
Q

two drugs to be aware of

A

Warfarin – lots of interactions – enzyme induction
Acute kidney injury – NSAIDs, ACEi