The Basics Flashcards
Pharmacodynamics
What the drug does to the body
Pharmacokinetics
What the body does to the drug
Ways drugs work
Via enzymes (ACE inhibitors) Receptor agonists (Salbutamol - beta agonist) Receptor antagonists (Atenolol - beta blocker)
Pharmacodynamic interactions
Occur when 2 drugs work via different pathways to effect the same outcome
Diuretics and ACE inhibitors
Aspirin and clopidogrel
Digoxin and beta blockers
Methods of absorption
Oral IV IM SC SL Topical Rectal Intra-articular/ intra-ocular
First pass metabolism
Oesophagus > Absorption in stomach > splanchnic circulation > metabolism in liver > blood stream
Distribution methods
Some drugs are lipophilic - distributed around whole body
Some are hydrophilic - stay in plasma
How are drugs metabolised in liver?
Lipophilic drug >
Phase 1 (oxidation/ reduction/ hydrolysis) >
Phase 2 (conjugation with glucuronide/ sulphate) >
Hydrophilic drug
Drugs metabolised by P450 system
Warfarin Theophylline Carbamazapine Phenytoin OCP
Inducers of P450 system
REDUCE efficacy of drug Carbamazapine Phenytoin Rifampicin Chronic alcohol intake BBQ meat St John's Wort
Inhibitors of P450 system
INCREASE efficacy of drug (toxicity) Erythromycin Ciprofloxacin Miconazole Sodium valproate Grapefruit juice Cranberry juice
Elimination
Hydrophilic drugs are excreted unchanged eg digoxin
Some lipophilic drugs are metabolised into active metabolites eg opioids
These may accumulate in renal failure
Drug half life
Time taken for the plasma concentration of a drug to decrease to 50% of the original value
Drug half life: dosing frequency, time to reach steady state, loading dose
Short half life:
QDS
Quicky reaches steady state
No loading dose needed
Long half life:
OD
Slowly reaches steady state
Loading dose needed
Therapeutic index
Effect that a drug has on the body is dependant on dose
If too low = no effect
Too high = toxic
Narrow therapeutic index needs to be monitored