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107 Cards in this Set

  • Front
  • Back
Clinical Pharmacology*
the study of drugs in humans
Drug
any chemical that can effect living processes
Therapeutics / Pharmotherapeutics*
the use of drugs to diagnose, prevent, or treat disease or to prevent pregnancy; or, the medical use of drugs
Pharmacology
the study of drugs and their interactions with living systems
Effective
an effective drug is one that elicits the responses for which it is given; the most important property a drug can have
Safety
a drug that cannot produce harmful effects; there is no such thing as a safe drug
Selective
a drug that elicits only the response for which it is given; there is no such thing as a selective drug
Metabolism
?
Excretion
?
Chemical Stability
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
Pharmodynamics
the impact of drugs on the body; pharmodynamic processes determine the nature and intensity of a response
Predictable Drug Response
difficult to ensure because each patient is unique; in order to maximize predictability we must tailor therapy to an individual
Receptor Binding
a drug binding to its receptor is the initial step leading to pharmodynamic processes
Pharmokinetics
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
Therapeutic Objective
maximum benefit with minimum harm
Biologic/Physiologic variations
age, weight, gender, etc
Receptor Binding
a drug binding to its receptor is the initial step leading to pharmodynamic processes
Pharmokinetics
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
Therapeutic Objective
maximum benefit with minimum harm
Biologic/Physiologic variations
age, weight, gender, etc
Assessment
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
Analysis
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
Planning
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
Implementation
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
Evaluation
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
Nonpharmacologic Measures
supportive measures to enhance drug therapy; e.g., enhancing drug therapy for asthma through breathing exercises
Patient Adherence
the extent to which a patient's behavior coincides with medical advice
Preadministration Assessment
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
Rights of Drug Administration
drug, patient, dose, route, time, documentation
Assessment
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
Analysis
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
Planning
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
Implementation
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
Evaluation
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
Nonpharmacologic Measures
supportive measures to enhance drug therapy; e.g., enhancing drug therapy for asthma through breathing exercises
Patient Adherence
the extent to which a patient's behavior coincides with medical advice
Preadministration Assessment
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
Rights of Drug Administration
drug, patient, dose, route, time, documentation
Precaution
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
Contraindication
a pre-existing condition that precludes use of a particular drug under all but the most desperate circumstances
Allergy and Anaphylaxis
?
Sensitivity and Cross-Sensitivity to Medication
?
PO
?
BID
?
prn
?
stat
?
Precaution
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
Contraindication
a pre-existing condition that precludes use of a particular drug under all but the most desperate circumstances
Therapeutic Responses
?
Sensitivity and Cross Sensivity to Medication
?
Approved Use of a Drug
?
Chemical Name
a description of a drug using the nomenclature of chemistry
Generic Name
assigned by the US Adopted Names Council; only one generic name, which is nonpropritary
Off-Label Use of a Drug
?
Investigational Drug
?
Postmarketing Surveillance
Phase 4 of new drug development; drug is released for general use and effects in general population are observed
Absoprtion
the movement of a drug from its site of administration into the blood
Bioavailability
absorption of the drug / the degree to which drug has been absorbed and is thus available
Biotransformation
drug metabolism; the enzymatic alteration of drug structure; most metabolism takes place in the liver
Chemical Equivalence
if multiple drugs contain the same amount of the identical chemical drug
Cytochrome P450 System
aka, the heptaic microsomal enzyme system; the system that performs drug metabolism in the liver
Distribution
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
Enteric Coated Preparations
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)
Enterohepatic Recirculation
?
Excretion
the removal of drugs from the body; mostly through urine, some through bile, but also through breast milk, expired air, sweat and saliva
Enteral / Enteral Routes
enteral routes of drug administration are through the GI tract
First Pass Effect
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
Half Life
the time required for the amount of drug in the body to decrease / decline by 50%
Hydrophillic / Hydrophobic
Water loving / water hating-fearing
Induction of Drug Metabolism
the stimulation of hepatic drug metabolizing enzymes can accelerate the metabolism of the inducing drug and other drugs
Ions
a charged particle created through ionization (when an acid donates a proton or a base receives a proton)
Lipid Soluble
can dissolve into lipids, ie, can dissolve directly into the lipid bilayer of a cell membrane
Loading Dose
a large initial dose given to achieve a plateau / therapeutic level quickly
Maintenance Dose
the dose given to maintain plateau
Metabolism
aka, biotransformation; the enzymatic alteration of drug structure
Minimum Effective Concentration (MEC)
the plasma drug level below which therapeutic effects will not occur
Parenteral / Parenteral Routes
by injection
Pharmokinetics
the study of drug movement throughout the body, it also includes drug metabolism and drug excretion; four basic processes- absorption, distribution, metabolism and excretion
Plateau
the point that should be achieved; it's reached after drug administered repeatedly- it usually takes 4 half lives to reach plateau
Polar Molecules
molecules with an uneven distribution of electric charge but no net charge (equal number of protons and electrons); e.g., water
Prodrug
a compound that is pharmacologically inactive as administered and then undergoes conversion to active form w/in the body
Protein Binding
drugs can form reversible bonds to proteins; most common protein this occurs with is albumin, which is so large it never leaves the blood
Quaternary
quaternary ammonium compounds are molecules that contain at least one atom of nitrogen and ALWAY care a positive charge
Sustained Release Preparations
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
Therapeutic Range
lies between the MEC and the toxic concentration; the objective of
Toxic Concentration
?
Affinity
the strength of attraction between a drug and its receptor
Agonist
molecules that activate receptors; they have both affinity and high intrinsic activity
Antagonist
drugs that prevent receptor activation by endogenous regulatory molecules and by other drugs
Competitive
aka, surmountable agents, they bind reversibly to receptors
Dose-Response Relationship
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
ED-50
the dose required to produce a defined therapeutic response in 50% of the population
Intrinsic Activity
the ability of a drug to activate a receptor upon binding
LD-50
the dose that is lethal to 50% of the animals treated
Maximal Efficacy
the largest effect that a drug can produce; indicated by the height of the dose response curve
Competitive Antagonist
when drugs compete for the same receptor site but don't potentiate the effects of the drugs; happens when drugs are highly protein bound
Noncompetitive Antagonist
binds irreversibly to receptors
Partial Agonist
have only moderate intrinsic activity; can act as agonists if no full agonist present or as antagonists if full agonist present
Pharmodynamics
the study of biochemical and physiologic effects of drugs and the molecular mechanisms by which those effects are produced
Potent
a potent drug is one that produces its effects at low levels; potency is not really important
Receptor
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
Therapeutic Index
a measure of a drug's safety; the
LD-50 to ED-50 ratio
Cytochrome P450 (CYP) System
?
Grapefruit Juice Effect
can inhibit intestinal metabolism of certain drugs, thereby increasing their absorption which in turn increases their blood levels; can last up to 3 days
Induction
?
Pharmodynamic Interaction
can be potentiative or inhibitory; they can act at the same site or act at separate sites
Pharmokinetic Interaction
may alter the absorption, distribution, metabolism or excretion of the other drug