1 Pharma Terms Flashcards
Amount that reaches the circulation
Bioavailability
Determine the safety and efficacy of generic drugs
Bioequivalence
Dose required to bring about 50% of the drug’s maximal effect
Potency
Dose at which 50% of the individuals exhibit the specified quantal effect
Median effective dose/ ED50
Dose at which 50% of the animals manifest a particular toxic effect
Median toxic dose/ TD50
Transfer of drug from site of admin to bloodstream
Volume of distribution
Elimination of the drug at CONSTANT rate
Zero order kinetics
Elimination at a rate that is proportional to the serum conc of the drug
First order kinetics
Addition of polar moiety (sulate, glucuronate, acetate)
Phase 2 (conjugation reaction)
Use of CYP 450 system (oxidation, reduction, hydrolysis)
Phase 1 (functionalization reaction)
Rate at which a specific drug is cleared from the system
Clearance
Amount of time required for the amount of the drug in the body to decrease to half its value after administration has been stopped
Half life (T 1/2)
Single amount of drug needed to achieve a desired plasma conc quickly
Loading dose
Amount of drug that must be given over time in order to maintain desired plasma conc
Maintenance dose
Measure of drug safety
Therapeutic index
Dose range between the minimum effective therapeutic dose or minimum toxic dose
Therapeutic window
Substance that shifts the graded dose response curve to the right
Competitive antagonist
Substance that does not produce the same maximum effect and is exhibited by a decrease in the Emax
Partial agonist
Substance that depresses the graded-dose response curve in the presence of the natural subtance
Irreversible antagonist