BRAINS and AIMS Flashcards

1
Q

BRAINS AIMS

-what does this stand for

A
Benefits
Risks
Adverse effects
Interactions
Necessary prophylaxis
Susceptible groups

Administering
Informing
Monitoring
Stopping

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2
Q

What are the risks involved in drug prescribing

A

Overdosing
Contraindications
Costs
Resistance to medication

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3
Q

How to deal with adverse reactions

A
Is it time or dose dependent
What drug is responsible
How would you correct the ADR
Stop ADR 
Report
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4
Q

What is a dose dependent adverse reaction

-what are the 3 types

A

Adverse reaction that is dependent on the amount of drug given

Supratherapeutic - toxic
-paracetamol OD
Therapeutic - side effects
-NSAID renal failure
-ACEi cough
Subtherapeutic - Hypersusceptible
-allergy
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5
Q

What are the dose dependent drugs that cause hepatitis

How would you recognise this?

A

Increase in ALT
Azathiopurine
Paracetamol

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6
Q

What are the dose independent drugs that cause hepatitis

How would you recognise this

A
Increase in ALT
Isoniazide, Pyrazinamide
Valproate
Methyldopa
Statins
NSAIDS
Phenytoin
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7
Q

What are the dose dependent drugs that cause cholestasis

How would you recognise this

A

Increase in AST and bilirubin
Rifampicin
Estrogen+Anabolic steroids

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8
Q

What are the dose independent drugs that cause cholestasis

How would you remember this
How would you recognise this

A

Increase in AST and bilirubin - Cl/Chl
Chlorpromazine - antipsychotic

Clarythromycin - ABx
Clavulanate-amox
Cloxacilin (flu)

Cimetidine - SSRI

Carbimazole - antithyroid

Chlorpropamide - sulphonylurea

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9
Q

What are the drugs that cause microvesicular steatosis

How would you remember this

A

VAT
Valproate
Aspirin
Tetracyclines

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10
Q

What are the drugs that cause macrovesicular steatosis

How would you remember this

A

Fatty liver, cirrhosis
AMA

Alcoholic hepatitis
Methotrexate
Amiodarone

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11
Q

What are time dependent ADRs

  • rapid
  • first dose
  • risk increases at first then decreaess
  • risk increases with time
  • withdrawal
  • delayed

What are examples of each one
How would you manage each type

A

Rapid - administer slowly
-IV vancomycin => Red man syndrome (systemic histamine release)

First dose - careful monitoring

  • ACEi => hypotension
  • penicilin => allergy

Risk increases at first then diminishes - warn patients of possible ADRs
-carbimazole, 5ASA (-salazines) => agranulocytosis (sore throat, increased bleeding risk, anemia)

Late - warn, monitor, prophylaxis if possible
-CS => osteoporosis

Withdrawal - warn, replace with longer acting drug if withdrawal not possible
-opiates, BZ, methyldopa(HTN), Bb => withdrawal symptoms

Delayed - avoid, screen, warn
-ciclosporin => carcinogen

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12
Q

What are the time independent ADRs

  • due to change in dose
  • due to change on concentration
  • due to neither

What are examples of each one
How would you manage each type

A

Change in dose from changed formulations
-stick to 1 brand for a patient

Change in concentration
-warn, monitor, reduce dosage, avoid interacting drugs

Due to neither
-warn, monitor, avoid interacting drugs

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13
Q

What are common examples of drugs that affect PO absorption

  • decrease GI motility
  • increase GI motility
A

Decrease GI motility

  • opiates
  • TCA

Increase GI motility
-metoclopromide (antiemetic)

Alter rate of absorption of other drugs

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14
Q

Describe the significance of displacement

-possible outcomes

A

Displaced drug => metabolised and excreted

Displaced from plasma proteins => increased toxicity, potency

  • ASA+NSAIDs => methotrexate toxicity if secretion impaired
  • ASA+NSAID+warfarin => increase bleeding risk
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15
Q

What are the methods of excretion

A

Glomerular filtration of unbound drug

Active tubular secretion
-ability reduced in renal failure

Passive tubular reabsorption

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16
Q

What are liver enzyme inducers
What do they do?

What are the drugs that do this
How would you remember this

A

Increase activity of liver enzymes
=> active drug broken down so less potent
=> inactive drug activated so more potent

PCBRAS
Phenytoin (antiepileptic)
Carbamazepine
Barbiturates, BBQ foods
Rifampicin
Alcohol (chronic)
St Johns Wort
17
Q

What are liver enzyme inhibitors
What do they do

What are the drugs that do this
How would you remember this

A

Decrease activity of liver enzymes
=> active drug not broken down
=> inactive drug not activated

GODEVICES
Grapefruit juice
Omeprazole
Disulfriam
Erythromycin
Valproate, 
Isoniazid
Cimetidine, 
Ethanol (acute)
Sulphonamides, 
Allopurinol
Metronidazole, ketoconazole
Ciprofloxacin
Verapamil, diltaizam, amiodarone
Chloramphenicol
SSRIs
18
Q

What are the clinically significant drugs with a narrow therapeutic range

How would you remember this

A

Small range where the drug concentration is safe and toxic

WAC STOPS
Warfarin
Antiarrythmics
Ciclosporin
Sulphonylureas
Theophyllines
Oral Contraceptives
Phenytoin
Steroids, statins
19
Q

Describe the interaction between SSRIs and liver enzymes

What is the danger when prescribing SSRIs and opioid pain relief

A

SSRIs (eg, fluoxetine, paroxetine) inhibit CYP2D6

Many opioids need to be activated by CYP2D6 => less effective if inhibited

Tramadol also has SNRI properties => increased risk of seretonin syndrome if coadministered with SSRIs

20
Q

What are the common interactions with warfarin

A

Protein binding displacement
-NSAIDs

Inhibit metabolism
-amiodarone, metronidazole, acute alcohol

Induction of liver metabolism

  • phenytoin
  • carbimazepine
  • barbiturates, BBQ
  • Rifampicin
  • Alcohol
  • St Johns Wort

Cranberry juice => increased INR

21
Q

Necassery prophylaxis for

  • NSAIDs
  • opioids
  • CS
A

NSAIDs => PPI (lansoprazole)

Opioids => laxatives, antiemetics

CS - if 3months, 7.5mg+ => alendronate

22
Q

Susceptibility mnemonic

-ASADGAP

A
Allergy
Sex
Age
Disease
Genetic
Altered physiology
Pregnancy, breast feeding
23
Q

What are women and men more susceptible to?

How would you reduce this risk

A

Use lower doses

Women

  • alcohol
  • ACEi cough
  • drug induced lupus
  • hepatitis - methyldopa
  • cholestasis - flucloxacilin

Men
-cholestasis - coamox

24
Q

What common drugs are older adults more susceptible to

How would you reduce this risk

A

Lower doses, monitor carefully but avoid where possible

Diuretics, antiHTN, Bb
Digoxin
NSAIDs
CNS drugs (BZ)
TCA
H1 antihistamines (chlorpheniramine)
H2 antagonists (ranitidine)
Opiates
25
Q

Describe how renal impairment may affect drugs

How would you approach this

A

Accummulation of renally cleared drugs

  • avoid drugs/reduced dose with narrow therapeutic range
  • increased nephrotoxicity of NSAIDs
26
Q

Describe how hepatic impairment may affect drugs

What drugs would this affect

A

CAFE METRO - altered PK, PD

Clotting reduced - warfarin, aspirin, NSAID
Albumin reduced - phenytoin, prednisolone toxicity
Fluid retention
Electrolyte imbalance - NSAIDs, steroids, furosemide
Metabolism reduced - opioids not activated or broken down
Encephalopathy - sedatives, hypoK (diuretics), opioids, constipators
Toxic liver drugs - NSAIDs => hepatitis, cholestasis, steatosis
Renal function impacted - NSAIDs

27
Q

Altered physiology susceptibility

  • pregnancy
  • drugs to avoid
A

Increased renal clearance of
-lithium, digoxin, penicillins => need to increase dose

Risk to fetus

  • thalidomide
  • phenytoin, valproate
  • warfarin, lithium
  • retinoids