lipidsolublethe amountof the drugthat reachessystemiccirculationeffectiveness,safety, &selectivitya measureof thedrug'ssafetyis limited to asmall # ofclients whotake the drugfor a shortperiod of timeevaluate therapeutic& adverse effects,identify high-riskpatients, & assesspatient's capacity forself-carethe oppositeof theintendeddrug effectmimic orblock thebody's ownregulatorymoleculesthe timerequired forthe amount ofthe drug toreduce by halfthe dose requiredto produce atherapeuticresponse in 50%of the populationconsists of 4processes:absorption,distribution,metabolism, &excretionthemaximumeffect thedrug canproduceprovidemaximumbenefit withminimumharmthe movementof a drug fromthe site ofadministrationto the bloodarandomized,double blind,controlledstudya drug-inducedbirthdefect30-60%aresometimesbeneficialtherapeutic response,adverse reactions &interactions, patientadherence, & patientsatisfaction withtreatmentalterations ingenes thatcode for drugmetabolizingenzymesthe dose shouldbe increased tomaintainbeneficialeffectsadministereither onehour beforeor two hoursafter a mealurticariathat act asagonistsat thatreceptorlipidsolublethe amountof the drugthat reachessystemiccirculationeffectiveness,safety, &selectivitya measureof thedrug'ssafetyis limited to asmall # ofclients whotake the drugfor a shortperiod of timeevaluate therapeutic& adverse effects,identify high-riskpatients, & assesspatient's capacity forself-carethe oppositeof theintendeddrug effectmimic orblock thebody's ownregulatorymoleculesthe timerequired forthe amount ofthe drug toreduce by halfthe dose requiredto produce atherapeuticresponse in 50%of the populationconsists of 4processes:absorption,distribution,metabolism, &excretionthemaximumeffect thedrug canproduceprovidemaximumbenefit withminimumharmthe movementof a drug fromthe site ofadministrationto the bloodarandomized,double blind,controlledstudya drug-inducedbirthdefect30-60%aresometimesbeneficialtherapeutic response,adverse reactions &interactions, patientadherence, & patientsatisfaction withtreatmentalterations ingenes thatcode for drugmetabolizingenzymesthe dose shouldbe increased tomaintainbeneficialeffectsadministereither onehour beforeor two hoursafter a mealurticariathat act asagonistsat thatreceptor

Pharmacology Fundamentals - Call List

(Print) Use this randomly generated list as your call list when playing the game. There is no need to say the BINGO column name. Place some kind of mark (like an X, a checkmark, a dot, tally mark, etc) on each cell as you announce it, to keep track. You can also cut out each item, place them in a bag and pull words from the bag.


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  1. lipid soluble
  2. the amount of the drug that reaches systemic circulation
  3. effectiveness, safety, & selectivity
  4. a measure of the drug's safety
  5. is limited to a small # of clients who take the drug for a short period of time
  6. evaluate therapeutic & adverse effects, identify high-risk patients, & assess patient's capacity for self-care
  7. the opposite of the intended drug effect
  8. mimic or block the body's own regulatory molecules
  9. the time required for the amount of the drug to reduce by half
  10. the dose required to produce a therapeutic response in 50% of the population
  11. consists of 4 processes: absorption, distribution, metabolism, & excretion
  12. the maximum effect the drug can produce
  13. provide maximum benefit with minimum harm
  14. the movement of a drug from the site of administration to the blood
  15. a randomized, double blind, controlled study
  16. a drug-induced birth defect
  17. 30-60%
  18. are sometimes beneficial
  19. therapeutic response, adverse reactions & interactions, patient adherence, & patient satisfaction with treatment
  20. alterations in genes that code for drug metabolizing enzymes
  21. the dose should be increased to maintain beneficial effects
  22. administer either one hour before or two hours after a meal
  23. urticaria
  24. that act as agonists at that receptor