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10 Cards in this Set

  • Front
  • Back
What is the bioavailability of IV vs Oral/Rectal?
IV - 100%
Oral/Rectal - <100%
What is the first pass effect?
How much drug is absorbed on first pass metabolism through the gut and liver
What are the characteristics of oral administration?
Easiest, but exposes drug to intestine/liver metabolism, which may inc first pass effect, CAN CAUSE EMESIS
What are the characteristics of Parenteral admistration (IV, IM, SubQ, Intraarterial / Intrathecal, Inhalation)?
IV - preferred for emergency, MOST DIRECT ROUTE
IM - drugs in aqueous solution
SubQ - only give small doses, slow metabolism, use for large pellets
IA/IT - used to put high concentrations in a specific organ
Inhalation - gaseous anesthetics, rapid absorption
What are the characteristics of Topical administration (Transdermal, buccal/sublingual, rectal)?
Transdermal - rapid + controlled penetration through the skin
B/S - self administered drugs that have high first pass metabolism, as this uses systemic veins, not portal circulation
Rectal - unconscious pt's or when oral route induces emesis, drugs do not pass through liver
What is stored in fat?
Lipid soluble drugs
What is stored in tissue (skeletal mm)?
Man drugs
What is stored in bone?
Tetracyclines
What is stored in plasma proteins?
Drugs that have a high degree of plasma protein binding, accumulate in plasma water
What are the 5 sites of drug exclusion?
CSF, ocular fluid, endolymph fluid, fetal fluid, pleural fluid