Concentration, time & dose Flashcards
amount in body mg=
volume (l) x concentration (mg/l)
initial concentration mg/l=
Dose (mg)/ volume (l)
half life=
ln(2) V / CL
constant rate infusion at steady state: concentration=
infusion rate/CL
properties of the concentration-effect profile that are important determinants of the drug effect:
cmax-highest concentration
tmax- time highest concentration is achieved
area under the curve
threshold concentration
slope-absorption & elimination
steady-state is?
where administration & elimination of a drug are in equilibrium
-reached at around 5 half-lives
phenytoin?
anti-epileptic drug and it can be used in an emergency situation to stop epileptic seizures
at what concentration is phenytoin efficacious at?
10-20 mg/L
in an ideal scenario a steady-state concentration can be done in emergency situation but not ideal for?
chronic conditions because it is inconvenient
how to calculate steady state? clearance-2L/hour
Vd= 70L
half life= ln(2) 70 / 2= 24 hours
24 x 5 - 120
so steady state is reached at around 120 hours
to get a therapeutic concentration quickly we need to give?
a loading dose
what is a loading dose?
an initial higher dose of a drug that may be given at the beginning of a course of treatment before dropping down to a lower maintenance dose
when do we use a loading dose?
used when elimination is slow/ when there is a desire to reach therapeutic concentration quickly
equation for first bolus dose:
concentration (mg/l) = dose (mg) / volume (l)
equation for loading dose
dose= conc x volume
vancomycin is?
an antibiotic with particular activity against gram positive bacterial infections
clinicians will administer what type of doses to achieve steady state? from calculating mean concentration
intermittent drug doses
intermittent dosing is favoured to giving a huge dose once a day as?
it avoids adverse effects
why do oral drugs have lower availability than IV drugs?
takes longer to reach systemic circulation
rosuvastatin is?
a statin that is used to lower cholesterol & prevent complications in patients with ischaemic heart disease
Cpss
mean concentration at steady state
F
bioavalabilty