BRAINS and AIMS Flashcards
BRAINS AIMS
-what does this stand for
Benefits Risks Adverse effects Interactions Necessary prophylaxis Susceptible groups
Administering
Informing
Monitoring
Stopping
What are the risks involved in drug prescribing
Overdosing
Contraindications
Costs
Resistance to medication
How to deal with adverse reactions
Is it time or dose dependent What drug is responsible How would you correct the ADR Stop ADR Report
What is a dose dependent adverse reaction
-what are the 3 types
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
What are the dose dependent drugs that cause hepatitis
How would you recognise this?
Increase in ALT
Azathiopurine
Paracetamol
What are the dose independent drugs that cause hepatitis
How would you recognise this
Increase in ALT Isoniazide, Pyrazinamide Valproate Methyldopa Statins NSAIDS Phenytoin
What are the dose dependent drugs that cause cholestasis
How would you recognise this
Increase in AST and bilirubin
Rifampicin
Estrogen+Anabolic steroids
What are the dose independent drugs that cause cholestasis
How would you remember this
How would you recognise this
Increase in AST and bilirubin - Cl/Chl
Chlorpromazine - antipsychotic
Clarythromycin - ABx
Clavulanate-amox
Cloxacilin (flu)
Cimetidine - SSRI
Carbimazole - antithyroid
Chlorpropamide - sulphonylurea
What are the drugs that cause microvesicular steatosis
How would you remember this
VAT
Valproate
Aspirin
Tetracyclines
What are the drugs that cause macrovesicular steatosis
How would you remember this
Fatty liver, cirrhosis
AMA
Alcoholic hepatitis
Methotrexate
Amiodarone
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
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
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
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
What are common examples of drugs that affect PO absorption
- decrease GI motility
- increase GI motility
Decrease GI motility
- opiates
- TCA
Increase GI motility
-metoclopromide (antiemetic)
Alter rate of absorption of other drugs
Describe the significance of displacement
-possible outcomes
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
What are the methods of excretion
Glomerular filtration of unbound drug
Active tubular secretion
-ability reduced in renal failure
Passive tubular reabsorption