NMP exam sample questions Flashcards
(120 cards)
Factors that affect absorption
- physico-chemical properties of drug
- drug formulation
- route of administration
what does ADME mean?
Absorption
Distribution
Metabolism
Excretion
Route of administration that will produce an enteral effect
Rectal
What is Bioavailability
The fraction of the dose which proceeds unaltered from the site of administration to the systemic circulation
Factors affecting bioavailability
- Poorly water soluble/slowly absorbed drug
- Malabsorption syndrome / GI surgery
- Increased gastric emptying time
- Complex formed e.g. tetracyclines and milk
- First pass effect
what is volume distribution?
pharmacokinetic parameter that represents the degree how a drug is distributed either remains in the plasma or redistribute to other tissues
It is the process of the body breaking down and converting medication into active chemical substances
Drug Metabolism
how many phase of metabolism is involved?
2 phases
What is phase 1 metabolism
- oxidation
- hydrolysis
- uses cytochome p450
- drug metabolite can still be chemically active
What is phase 2 metabolism
- conjugation
- attachment of an ionised group to the drug
- reduces drug effect
makes metabolite more water soluble for excretion
Factors affecting drug metabolism
- Enzyme induction
- Enzyme inhibition
- genetic deficiency
- age
- liver disease
What the drug does to the body
Pharmacodynamics
Examples of neurotransmitters
- Acetylcholine (ACh)
- Histamine (H)
- Dopamine (DA)
- Noradrenaline (NA)
- Adrenaline (Adr)
- 5-Hydroxytriptamine (5-HT) [serotonin]
Factors affecting drug excretion
- blood flow to kidney (normal 1500ml/min)
- glomerular filtration rate (normal 100mls/min)
- active secretion of drugs into the kidney tubule (e.g. penicillin)
- passive reabsorption back into the tubule
is an important consideration influencing distribution
Protein binding
Will plasma protein binding increase or decrease the volume of distribution?
decrease
what is half life
Half-life is the time taken for the concentration of drug in blood to fall by half
A patient showing toxic side effects of a drug has her plasma drug concentration measured. It is 100mg/L. The normal range is 20-30mg/L. If the half life is 24 hours how long before the level drops back to within the normal range?
Computation: 100mg half in 24hours
(First half life) 50mg = 24hours
(Second half life) 25mg = 48hours (normal range 20 to 30mg)
Answer:
2 days:
o After 24 hours the level will be 50mg/L
o After 48 hours the level will be 25mg/L
Recommend omit drug for 2 days, then re-start using lower dose.
is the amount of a medication between the quantity that gives the effective dose and the amount that gives more adverse than desired effects
Therapeutic window
The ability of a drug to produce an effect
Drug efficacy
Loss of response to a drug usually due to a decrease in number of receptors
Desensitisation
give 3 examples of narrow therapeutic index drugs
lithium
gentamycin
theophylline
digoxin
phenytoin
warfarin
The term for a drug that blocks the effects of a neurotransmitter at (or near) the receptor sites
Antagonist
Condition that may follow after repeated exposure to a drug in so that the effect produced by the original dose no longer occurs i.e. increasing doses required to achieve the same effect
Drug tolerance