adverse drug reactions Flashcards

1
Q

how to classify ADRs

A

based on onset, severity, and type

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2
Q

onset- time of acute, subacute and latent

A

acute within an hour (eg anaphylaxis), sub-acute (1-24 hrs), latent after 2 days

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3
Q

severity-mild, moderate, and severe

A

mild requires no change, moderate does+hospitalisation, and severe can be life-threatening

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4
Q

type A with examples

A

AUGMENTED: most common- predictable and dose dependent eg NSAIDS and ulcers, or anticholingergics and dry mouth

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5
Q

DIAGRAM ADR in paracetamol vs digoxin

A

digoxin ADR linear- paracetamol usually harmless, until suddenly effects become toxic

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6
Q

type B reactions

A

BIZARRE: rare and unpredictable- often immunological reactions causing allergy/pseudoallergies

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7
Q

type C reactions

A

caused by CHRONIC use, which leads to accumulation of drugs eg methotrexate and fibrosis of liver

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8
Q

type D

A

DELAYED effects, which can be carcinogenic eg immunosurpressants

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9
Q

type E- different type

A

END (E=end) of treatment-either withdrawal reactions (problems when stop taking drug) or rebound reactions (situation gets worse when drug stopped)

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10
Q

example of rebound reations

A

when taking clonidine, BP goes down, but when stopped, BP goes up even higher

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11
Q

examples of pseudoallergies ie not really allergies

A

NSAIDS lead to bronchospasm, ACE inhibitors lead to cough/angioedema (swelling of lips)

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12
Q

common drugs causing ADRS

A

antibiotics, anticoagulants, CVS drugs, NSAIDS, CNS drugs

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13
Q

problem with ADR detection

A

rare events often not detected until drug is licensed

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14
Q

yellow card scheme

A

way for clinicians reporting any adverse drug reactions for new drugs, and SERIOUS ADRS for common drugs

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15
Q

types of drug interactions

A

pharmacodynamic (drugs effect on body ie competing for receptora), pharmacokinetics (body’s effect on drug eg absorption/metabolism), and pharmaceutical (interaction of drugs outside body)

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16
Q

pharmacodynamic interactions- types

A

can be additive effect eg ethanol and benzodiazepines or antagonist eg anticholingergic

17
Q

types of pharmacokinetic interactions- change in absoprtion- CHELATION wit example

A

drugs bind together= less absorption eg antibiotics

18
Q

types of pharmacokinetic- protein binding interactions and importance, with example

A

drugs compete for plasma proteins- often not important but eg warfarin

19
Q

types of pharmacokinetic- difference metabolism+ CYP450 inhibitor examples

A

multiple drugs compete for same P450 enzymes, particularly when given a CYP450 inhibitor eg antibiotics+ HIV drugs

20
Q

CYP450 inducers

A

rifampicin and St johns wort

21
Q

most important P450 enzyme

A

CYP450 3A4

22
Q

inducers vs inhibitors

A

inhibition rapid vs inducers longer (as takes time to make new Cyp450 enzymes)

23
Q

types of pharmacokinetic- elimination reactions with examples

A

occurs in renal tubule- pencillin leads to more elimination, lithium leads to less