Adverse drug reations Flashcards

1
Q

What percentage of hospital admissions do ADRs occur in?

A

5%

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2
Q

What percentage of hospital patients suffer an ADR?

A

10-20%

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3
Q

What percentage of hospital deaths occur due to ADRs?

A

0.3- 3%

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4
Q

Describe the 3 classes of onset of ADRs and give examples

A

Acute - within 60 minutes - bronchonstriction
Sub- Acute - 1-24 hours - rash, serum sickness
Latent - > 2 days - eczematous eryptions

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5
Q

Give the classifications of ADRS

A
A - Augmented
B - Bizarre
C - Chronic
D - Delayed
E - End of treatment
F - Failure of treatment
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6
Q

Describe type A ADRS

A

Predictable, dose related effects that resolve when the drug is reduced or stopped
Normally due to pharmokinetic/ pharmodynamic variation

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7
Q

What factors lead to pharmokinetic variation

A

altered absorption, distribution, metabolism and excretion

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8
Q

What factors lead to pharmodynamic variation

A

disease state eg. renal/ hepatic variation

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9
Q

Describe Type B ADRs

A

Bizarre, unpredictable, rare and serious
Not related to dose
immunological or idiosyncratic (inherit abnormal response eg. enzyme deficiency)

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10
Q

Describe type C ADRs

A

Related to duration of treatment and dose dependent
Pro longed and semi- predictable
eg. steroid induced osteoporosis, opiate dependence

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11
Q

Describe type D ADRs

A

Occur some time after treatment
eg. carcinogenesis from alkylating agents/ immunosuppressants
teterogenisis - passed from mother to child (uteroexposure)

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12
Q

Describe type E ADRs

A

Occurs when drugs are stopped suddenly
eg. seizures from no alcohol
Addison crisis after long term steroids (heavily suppressed adrenal gland)

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13
Q

Describe type F ADRs

A

Common and dose related

Caused by mistakes

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14
Q

What is the most common cause of type F ADRs

A

drug - drug interactions

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15
Q

How may you detect an ADR

A

Medication history
Assess onset time in relation to dose
Investigate plasma concentration
Allergy tests

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16
Q

How may you report an ADR

A

Yellow card - voluntary reporting to CSM (committee of safety of medicines)
anecdotal reporting
event recording