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107 Cards in this Set
- Front
- Back
Clinical Pharmacology*
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the study of drugs in humans
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Drug
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any chemical that can effect living processes
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Therapeutics / Pharmotherapeutics*
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the use of drugs to diagnose, prevent, or treat disease or to prevent pregnancy; or, the medical use of drugs
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Pharmacology
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the study of drugs and their interactions with living systems
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Effective
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an effective drug is one that elicits the responses for which it is given; the most important property a drug can have
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Safety
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a drug that cannot produce harmful effects; there is no such thing as a safe drug
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Selective
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a drug that elicits only the response for which it is given; there is no such thing as a selective drug
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Metabolism
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Excretion
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Chemical Stability
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the degree to which / whether or not drugs lose effectiveness in storage, put in solution, or lose efficacy in some other way; stability is a property of an ideal drug
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Pharmodynamics
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the impact of drugs on the body; pharmodynamic processes determine the nature and intensity of a response
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Predictable Drug Response
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difficult to ensure because each patient is unique; in order to maximize predictability we must tailor therapy to an individual
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Receptor Binding
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a drug binding to its receptor is the initial step leading to pharmodynamic processes
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Pharmokinetics
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The impact of the body on drugs; Four processes that determine how much of an administered dose gets to its site(s) of action;
1) drug absorption 2) drug distribution 3) drug metabolism 4) drug excretion |
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Therapeutic Objective
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maximum benefit with minimum harm
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Biologic/Physiologic variations
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age, weight, gender, etc
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Receptor Binding
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a drug binding to its receptor is the initial step leading to pharmodynamic processes
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Pharmokinetics
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The impact of the body on drugs; Four processes that determine how much of an administered dose gets to its site(s) of action;
1) drug absorption 2) drug distribution 3) drug metabolism 4) drug excretion |
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Therapeutic Objective
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maximum benefit with minimum harm
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Biologic/Physiologic variations
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age, weight, gender, etc
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Assessment
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Step 1 of Nursing Process; collecting data about patient using methods such as patient interview, medical and drug use histories, physical examination, observation and laboratory tests
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Analysis
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also, Nursing Diagnoses; Step 2 of the Nursing Process; analysis of database to determine actual and potential health problems that could be physiologic, psychologic or sociologic; consists of a statement of problems or potential problems and a statement of the problem's probably cause or risk factors
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Planning
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Step 3 of the Nursing Process; delineation of specific interventions for solving or preventing problems; defines goals, sets priorities, identifies nursing interventions and establishes criteria for evaluating success
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Implementation
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Step 4 of Nursing Process; carries out intervention, it may be collaborative (requiring a physician's order) or independent; involves observing and recording outcomes of treatment
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Evaluation
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Step 5 of Nursing Process; determine the degree to which treatment has succeeded by analyzing the data collected during implementation; determines what should be continued/discontinued and potential new interventions
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Nonpharmacologic Measures
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supportive measures to enhance drug therapy; e.g., enhancing drug therapy for asthma through breathing exercises
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Patient Adherence
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the extent to which a patient's behavior coincides with medical advice
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Preadministration Assessment
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the beginning of drug therapy; its goals are 1) collect baseline data needed to evaluate therapeutic and adverse responses 2) identify high-risk patients 3) assess the patient's capacity for self-care
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Rights of Drug Administration
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drug, patient, dose, route, time, documentation
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Assessment
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Step 1 of Nursing Process; collecting data about patient using methods such as patient interview, medical and drug use histories, physical examination, observation and laboratory tests
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Analysis
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also, Nursing Diagnoses; Step 2 of the Nursing Process; analysis of database to determine actual and potential health problems that could be physiologic, psychologic or sociologic; consists of a statement of problems or potential problems and a statement of the problem's probably cause or risk factors
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Planning
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Step 3 of the Nursing Process; delineation of specific interventions for solving or preventing problems; defines goals, sets priorities, identifies nursing interventions and establishes criteria for evaluating success
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Implementation
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Step 4 of Nursing Process; carries out intervention, it may be collaborative (requiring a physician's order) or independent; involves observing and recording outcomes of treatment
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Evaluation
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Step 5 of Nursing Process; determine the degree to which treatment has succeeded by analyzing the data collected during implementation; determines what should be continued/discontinued and potential new interventions
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Nonpharmacologic Measures
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supportive measures to enhance drug therapy; e.g., enhancing drug therapy for asthma through breathing exercises
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Patient Adherence
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the extent to which a patient's behavior coincides with medical advice
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Preadministration Assessment
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the beginning of drug therapy; its goals are 1) collect baseline data needed to evaluate therapeutic and adverse responses 2) identify high-risk patients 3) assess the patient's capacity for self-care
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Rights of Drug Administration
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drug, patient, dose, route, time, documentation
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Precaution
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a pre-existing condition that significantly increases the risk of an adverse reaction to a particular drug, but not to a degree that is life threatening
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Contraindication
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a pre-existing condition that precludes use of a particular drug under all but the most desperate circumstances
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Allergy and Anaphylaxis
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Sensitivity and Cross-Sensitivity to Medication
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PO
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BID
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prn
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stat
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Precaution
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a pre-existing condition that significantly increases the risk of an adverse reaction to a particular drug, but not to a degree that is life threatening
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Contraindication
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a pre-existing condition that precludes use of a particular drug under all but the most desperate circumstances
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Therapeutic Responses
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Sensitivity and Cross Sensivity to Medication
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Approved Use of a Drug
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Chemical Name
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a description of a drug using the nomenclature of chemistry
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Generic Name
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assigned by the US Adopted Names Council; only one generic name, which is nonpropritary
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Off-Label Use of a Drug
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Investigational Drug
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Postmarketing Surveillance
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Phase 4 of new drug development; drug is released for general use and effects in general population are observed
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Absoprtion
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the movement of a drug from its site of administration into the blood
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Bioavailability
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absorption of the drug / the degree to which drug has been absorbed and is thus available
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Biotransformation
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drug metabolism; the enzymatic alteration of drug structure; most metabolism takes place in the liver
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Chemical Equivalence
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if multiple drugs contain the same amount of the identical chemical drug
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Cytochrome P450 System
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aka, the heptaic microsomal enzyme system; the system that performs drug metabolism in the liver
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Distribution
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the movement of drugs throughout the body; determined by blood flow to tissues, the ability of a drug to exit the vascular system and a bit by the ability of a drug to enter cells
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Enteric Coated Preparations
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a method or oral preparation; drugs that have been covered with a material designed to dissolve in the intestine but not the stomach (to protect drugs from pepsin and to protect stomach from drugs that can cause gastric discomfort)
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Enterohepatic Recirculation
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Excretion
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the removal of drugs from the body; mostly through urine, some through bile, but also through breast milk, expired air, sweat and saliva
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Enteral / Enteral Routes
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enteral routes of drug administration are through the GI tract
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First Pass Effect
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the rapid hepatic inactivation of some oral drugs as they pass through the liver; can happen with drugs that the liver has is extremely good at metabolizing
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Half Life
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the time required for the amount of drug in the body to decrease / decline by 50%
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Hydrophillic / Hydrophobic
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Water loving / water hating-fearing
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Induction of Drug Metabolism
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the stimulation of hepatic drug metabolizing enzymes can accelerate the metabolism of the inducing drug and other drugs
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Ions
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a charged particle created through ionization (when an acid donates a proton or a base receives a proton)
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Lipid Soluble
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can dissolve into lipids, ie, can dissolve directly into the lipid bilayer of a cell membrane
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Loading Dose
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a large initial dose given to achieve a plateau / therapeutic level quickly
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Maintenance Dose
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the dose given to maintain plateau
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Metabolism
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aka, biotransformation; the enzymatic alteration of drug structure
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Minimum Effective Concentration (MEC)
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the plasma drug level below which therapeutic effects will not occur
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Parenteral / Parenteral Routes
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by injection
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Pharmokinetics
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the study of drug movement throughout the body, it also includes drug metabolism and drug excretion; four basic processes- absorption, distribution, metabolism and excretion
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Plateau
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the point that should be achieved; it's reached after drug administered repeatedly- it usually takes 4 half lives to reach plateau
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Polar Molecules
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molecules with an uneven distribution of electric charge but no net charge (equal number of protons and electrons); e.g., water
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Prodrug
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a compound that is pharmacologically inactive as administered and then undergoes conversion to active form w/in the body
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Protein Binding
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drugs can form reversible bonds to proteins; most common protein this occurs with is albumin, which is so large it never leaves the blood
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Quaternary
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quaternary ammonium compounds are molecules that contain at least one atom of nitrogen and ALWAY care a positive charge
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Sustained Release Preparations
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capsules filled with tiny spheres that contain the actual drug, and the coating of the spheres dissolve at variable rates; advantageous because they permit a reduction in number of daily doses and producing steady drug levels over an extended time; the disadvantages are that they're expensive and have potential for variable absorption
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Therapeutic Range
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lies between the MEC and the toxic concentration; the objective of
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Toxic Concentration
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Affinity
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the strength of attraction between a drug and its receptor
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Agonist
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molecules that activate receptors; they have both affinity and high intrinsic activity
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Antagonist
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drugs that prevent receptor activation by endogenous regulatory molecules and by other drugs
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Competitive
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aka, surmountable agents, they bind reversibly to receptors
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Dose-Response Relationship
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the relationship between the size of an administered dose and the intensity of the response produced; they determine the minimum amount of a drug we can use and the maximum response a drug can elicit and how much we need to increase dosage in order to produce the desired increase in response
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ED-50
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the dose required to produce a defined therapeutic response in 50% of the population
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Intrinsic Activity
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the ability of a drug to activate a receptor upon binding
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LD-50
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the dose that is lethal to 50% of the animals treated
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Maximal Efficacy
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the largest effect that a drug can produce; indicated by the height of the dose response curve
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Competitive Antagonist
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when drugs compete for the same receptor site but don't potentiate the effects of the drugs; happens when drugs are highly protein bound
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Noncompetitive Antagonist
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binds irreversibly to receptors
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Partial Agonist
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have only moderate intrinsic activity; can act as agonists if no full agonist present or as antagonists if full agonist present
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Pharmodynamics
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the study of biochemical and physiologic effects of drugs and the molecular mechanisms by which those effects are produced
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Potent
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a potent drug is one that produces its effects at low levels; potency is not really important
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Receptor
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a macromolecule in a cell that a drug binds to; 4 families of receptors are cell membrane-embedded enzymes, ligand-gated ion channels, G protein-coupled receptor systems, and transcription factors
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Therapeutic Index
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a measure of a drug's safety; the
LD-50 to ED-50 ratio |
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Cytochrome P450 (CYP) System
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Grapefruit Juice Effect
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can inhibit intestinal metabolism of certain drugs, thereby increasing their absorption which in turn increases their blood levels; can last up to 3 days
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Induction
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Pharmodynamic Interaction
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can be potentiative or inhibitory; they can act at the same site or act at separate sites
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Pharmokinetic Interaction
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may alter the absorption, distribution, metabolism or excretion of the other drug
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