Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
168 Cards in this Set
- Front
- Back
Drug
|
Chemical used to diagnose, treat, or prevent disease
|
|
Pharmacology
|
The study of drugs and their interactions with the body
|
|
Types of Drug Names
|
1. Chemical name
2. Generic name 3. Official name 4. Brand name |
|
Drug Classification
|
The broad group to which the drug belongs.
|
|
Mechanism of Action
|
The way in which a drug causes its effects; its pharmacodynamics
|
|
Indications
|
Conditions that make administration of the drug appropriate (as approved by the Food and Drug Administration)
|
|
Pharmacokinetics
|
How the drug is absorbed, distributed, and eliminated; typically includes onset and duration of action
|
|
Side Effects/Adverse Reactions
|
The drug's untoward or undesired effects
|
|
Routes of Administration
|
How the drug is given
|
|
Contraindications
|
Conditions that make it inappropriate to give the drug. Unlike when the drug is simply not indicated, a contraindication means that a predictable harmful event will occur if the drug is given in this situation
|
|
Dosage
|
The amount of the drug that should be given
|
|
How Supplied
|
This typically includes the common concentrations of the available preparations; many drugs come in different concentrations
|
|
Special Considerations
|
How the drug may affect pediatric, geriatric, or pregnant patiens
|
|
Assay
|
Test that determines the amount and purity of a given chemical in a preparation in the laboratory
|
|
Bioequivalence
|
Relative therapeutic effectiveness of chemically equivalent drugs
|
|
Bioassay
|
Test to ascertain a drug's availability in a biological model
|
|
Phase 1 of human drug studies
|
Testing to determine the drug's pharmacokinetics, toxicity, and safe dose in humans. Limited populations of healthy human volunteers.
|
|
Phase 2 of human drug studies
|
Primary purpose to find the therapeutic drug level and watch carefully for toxic and side effects
|
|
Phase 3 of human drug studies
|
Primary purpose to refine the usual therapeutic dose and to collect relevant data on side effects. Usually double blind
|
|
Phase 4 of human drug studies
|
Postmarketing analysis during conditional approval. FDA requires that drug makers monitor performance to discontinue if perviously unknown effects become apparent.
|
|
Six rights of medication administration
|
1. Right Medication
2. Right Dose 3. Right Time 4. Right route 5. Right patient 6. Right documentation |
|
Dose packaging
|
Medication packages contain a single dose for a single patient
|
|
Teratogenic drug
|
Medication that may deform or kill the fetus
|
|
Free drug availability
|
Proportion of a drug available in the body to cause either desired or undesired effects
|
|
Pharmacokinetics
|
How a drug is absorbed, distributed, metabolized (Biotransformed), and excreted; how drugs are transported into and out of the body
|
|
Pharmacodynamics
|
How a drug interacts with the body to cause its effects
|
|
Active Transport
|
Requires the use of energy to move a substance
|
|
Carrier-mediated diffusion or facilitated diffusion
|
Process in which carrier proteins transport large molecules across the cell membrane
|
|
Passive transport
|
Movement of a substance without the use of energy
|
|
Diffusion
|
Movement of solute in a solution from an area of higher concentration to an area of higher concentration to an area of lower concentration
|
|
Osmosis
|
Movement of solvent in a solution from an area of lower solute concentration to an area of higher solute concentration
|
|
Filtration
|
Movement of molecules across a membrane from an area of higher pressure to an area of lower pressure
|
|
Pharmacokinetic Processes
|
1. Absorption
2. Distribution 3. Biotransformation 4. Elimination |
|
Ionize
|
To become electrically charged or polar
|
|
Bioavailability
|
Amount of a drug that is still active after it reaches its target tissue
|
|
Blood-brain barrier
|
Tight junctions of the capillary endothelial cells in the cintral nervous system vasculature through which only non-protein-bound highly lipid-soluble drugs can pass
|
|
Placental barrier
|
Biochemical barrier at teh maternal/fetal interface that restricts certain molecules
|
|
Metabolism
|
The body's breaking down chemicals into different chemicals
|
|
Biotransformation
|
Speical name given to the metabolism of drugs
|
|
Prodrug (parent drug)
|
Medication that is not active when administered, but whose biotransformation converts it into active metabolites
|
|
First-pass effect
|
The liver's partial or complete inactivation of a drug before it reaches the systemic circulation
|
|
Oxidation
|
The loss of hydrogen atoms or the acceptance of an oxygen atom. This increases the positive charge (or lessens the negative charge) on the molecule
|
|
Hydrolysis
|
The breakage of a chemical bond by adding water, or by incorporating a hydroxyl (OH-) group into one fragment and a hydrogen ion (H+) into the other
|
|
Enteral route
|
Delivery of a medication through the gastrointestinal tract
|
|
Parenteral route
|
Delivery of a medication outside of the gastrointenstinal tract, typically using needles to inject medications into the circulatory system or tissues
|
|
Types of drug actions
|
1. Binding to a receptor site
2. Changing the physical properties of cells 3. Chemically combining with other chemicals 4. Altering a normal metabolic pathway |
|
Receptor
|
Specialized protein that combines with a drug resulting in a biochemical effect
|
|
Affinity
|
Force of attraction between a drug and a receptor
|
|
Efficacy
|
A drug's ability to cause the expected response
|
|
Second messenger
|
Chemical that participates in complex cascading reactions that eventually cause a drug's desired effect
|
|
Down-regulation
|
Binding of a drug or hormone to a target cell receptor that causes the number of receptors to decrease
|
|
Up-regulation
|
A drug causes the formation of more receptors than normal
|
|
Agonist
|
Drug that binds to a receptor and causes it to initiate the expected response
|
|
Antagonist
|
Drug that binds to a receptor but does not cause it it initiate the expected response
|
|
Agonist-Antagonist (partial agonist)
|
Drug that binds to a receptor and stimulates some of its effects but blocks others
|
|
Competitive antagonism
|
One drug binds to a receptor and causes the expected effect while also blocking another drug from triggering the same receptor
|
|
Noncompetitive antagonism
|
The binding of an antagonist causes a deformity of the binding site that prevents an agonist from fitting and binding
|
|
Irreversible antagonism
|
A competitive antagonist permanently binds with a receptor site
|
|
Side effect
|
Unintended response to a drug
|
|
Allergic Drug Reaction
|
Also known as hypersensitivity this effect occurs as the drug is antigenic and activates the immune system, causing effects that are normally more profound than seen in the general population
|
|
Drug Idiosyncrasy
|
A drug effect that is unique to the individual: different than seen or expected in the population in general
|
|
Drug Tolerance
|
Decreased response to the same amount of drug after repeated administrations
|
|
Drug Cross-Tolerance
|
Tolerance for a drug that develops after administration of a different drug.
|
|
Drug Tachyphylaxis
|
Rapidly occurring tolerance to a drug. May occur after a single dose.
|
|
Cumulative drug effect
|
Increased effectiveness when a drug is given in several doses
|
|
Blood-brain barrier
|
Tight junctions of the capillary endothelial cells in the cintral nervous system vasculature through which only non-protein-bound highly lipid-soluble drugs can pass
|
|
Placental barrier
|
Biochemical barrier at teh maternal/fetal interface that restricts certain molecules
|
|
Metabolism
|
The body's breaking down chemicals into different chemicals
|
|
Biotransformation
|
Speical name given to the metabolism of drugs
|
|
Prodrug (parent drug)
|
Medication that is not active when administered, but whose biotransformation converts it into active metabolites
|
|
First-pass effect
|
The liver's partial or complete inactivation of a drug before it reaches the systemic circulation
|
|
Oxidation
|
The loss of hydrogen atoms or the acceptance of an oxygen atom. This increases the positive charge (or lessens the negative charge) on the molecule
|
|
Hydrolysis
|
The breakage of a chemical bond by adding water, or by incorporating a hydroxyl (OH-) group into one fragment and a hydrogen ion (H+) into the other
|
|
Enteral route
|
Delivery of a medication through the gastrointestinal tract
|
|
Parenteral route
|
Delivery of a medication outside of the gastrointenstinal tract, typically using needles to inject medications into the circulatory system or tissues
|
|
Receptor
|
Specialized protein that combines with a drug resulting in a biochemical effect
|
|
Affinity
|
Force of attraction between a drug and a receptor
|
|
Efficacy
|
A drug's ability to cause the expected response
|
|
Second Messenger
|
Chemical that participates in complex cascading reactions that eventually cause a drug's desired effect
|
|
Down-Regulation
|
Binding of a drug or hormone to a target cell receptor that causes the number of receptors to decrease
|
|
Up-Regulation
|
A drug causes the formation of more receptors than normal
|
|
Agonist
|
Drug that binds to a receptor and causes it to initiate the expected response
|
|
Antagonist
|
Drug that binds to a receptor but does not cause it to initiate the expected response
|
|
Agonist-Antagonist (partial agonist)
|
Drug that binds to a receptor and stimulates some of its effects but blocks others
|
|
Competititve Antagonism
|
One drug binds to a receptor and causes the expected effect while also blocking another drug from triggering the same receptor
|
|
Noncompetitive Antagonism
|
The binding of an antagonist causes a deformity of the binding site that prevents an agonist from fitting and binding
|
|
Irreversible antagonism
|
A competitive antagonist permanently binds with a receptor site
|
|
Side effect
|
Unintended response to a drug
|
|
Drug Allergic reaction
|
Also known as hypersensitivity; this effect occurs as the drug is antigenic and activates the immune system, causing effects that are normally more profound than seen in the general population
|
|
Drug Idiosyncrasy
|
A drug effect that is unique to the individual; different than seen or expected in the population in general
|
|
Drug Cross-tolerance
|
Tolerance for a drug that develops after administration of a different drug.
|
|
Drug Tachyphylaxis
|
Rapidly occurring tolerance to a drug. May occur after a single dose. Typically occurs with sympathetic agonist.
|
|
Drug Cumulative Effect
|
Increased effectiveness when a drug is given in several doses
|
|
Drug Dependence
|
The patient becomes accoustomed to the drug's presence in his body and will suffer from withdrawal symptoms upon its absence
|
|
Drug Interaction
|
The effects of on drug alter ther response to another
|
|
Drug Antagonism
|
The effects of one drug block the response to another drug
|
|
Drug Summation
|
Also known as an additive effect. Two drugs that both have the same effect are given together, analogous to 1+1=2
|
|
Drug Synergism
|
Two drugs that both have teh same effect are given together and produce a response greater than the sum of their individual responses, analogous to 1+1=3
|
|
Drug Potentiation
|
One drug enhances the effect of another.
|
|
Drug Interference
|
The direct biochemical interaction between two drugs; one drug affects the pharmacology of another drug
|
|
Drug-response relationship
|
Correlation of different amounts of a drug to clinical response
|
|
Plasma-level profile
|
Describes the lengths of onset, duration, and termination of action, as well as the drug's minimum effective concentration and toxic levels
|
|
Onset of action
|
The time from administration until a medication reaches its minimum effective concentration
|
|
Minimum effective concentration
|
Minimul level of drug needed to cause a given effect
|
|
Duration of action
|
Length of time the amount of drug remains above its minimum effective concentration
|
|
Onset of action
|
The time from administration until a medication reaches its minimum effective concentration
|
|
Minimum effective concentration
|
Minimum level of drug needd to cause a given effect
|
|
Duration of action
|
Length of time the amount of drug remains above its minimum effective concentration
|
|
Termination of action
|
Time from when the drug's level drops below its minimum effective concentration until it is eliminated from the body
|
|
Therapeutic index
|
Ratio of a drug's lethal dose for 50 percent of the population to its effective dose for 50 percent of the population
|
|
Biologic half-life
|
Time the body takes to clear one half of a drug
|
|
Factors Affecting Drug-Response Relationship
|
Age - Body mass - Sex - Environment - Time of administration - Pathology - Genetics - Psychology
|
|
Prototype
|
Drug that best demonstrates the class's common properties and illustrates its particular characteristics
|
|
Analgesic
|
Medication that relieves the sensation of pain
|
|
Analgesia
|
The absence of the sensation of pain
|
|
Anesthesia
|
The absence of all sensations
|
|
Adjunct medication
|
Agent that enhances the effects of other drugs
|
|
Anesthetic
|
Medication that induces a loss of sensation to touch or pain
|
|
Neuroleptanesthesia
|
Anethesia that combines decreased sensation of pain with amnesia while the patient remains conscious
|
|
Sedation
|
State of decreased anxiety and inhibitions
|
|
Hypnosis
|
Instigation of sleep
|
|
Psychotherapeutic medication
|
Drug used to treat mental dysfunction
|
|
Extrapyramidal symptoms (EPS
|
Common side effects of antipsychotic medications, including muscle tremors and parkinsonism-like effects
|
|
Neuroleptic
|
Antipsychotic (literally, affecting the nerves)
|
|
Major Classes of Antipsychotic meds
|
1. Phenothiazines
2. Butyrophenones 3. Atypicals |
|
Major Classes of Antidepressant Meds
|
1. TCAs (Tricyclic)
2. SSRIs (Selective Serotonin Reuptake Inhibitors) 3. MAOIs (Monoamine Neurotransmitters) |
|
Autonomic Nervous system
|
The part of the nervous system that controls involuntary actions
|
|
Autonomic ganglia
|
Groups of autonomic nerve cells located outside the central nervous system
|
|
Preganglionic nerves
|
Nerve fibers that extend from the central nervous system to the autonomic ganglia
|
|
Postganglionic nerves
|
Nerve fibers that extend from the autonomic ganglia to the target tissue
|
|
Synapse
|
Space between nerve cells
|
|
Neuroeffector junction
|
Specialized synapse between a nerve cell and the organ or tissue it innervates
|
|
Neurotransmitter
|
Chemical messenger that conducts a nervous impulse across a synapse
|
|
Neuron
|
Nerve cell
|
|
Cholinergic
|
Pertaining to the neurotransmitter acetylcholine
|
|
Adrenergic
|
Pertaining to the neurotransmitter norepinephrine
|
|
Cranial nerves carryin Parasympathetic fibers
|
Nerves III - VII - IX - X
|
|
Parasympathomimetic (or anticholinergic)
|
Drug or other substance that causes effects like those of the parasympathetic nervous system
|
|
Direct acting Cholinergics (Cholinergic esters)
|
Drugs that stimulate the effects of ACh by directly binding with the cholinergic receptors.
|
|
Indirect acting Cholinergics
|
Drugs that affect acetylcholinesterase By inhibiting its actions in degrading acetylcholine they prolong the cholinergic response.
|
|
Sympathomimetic (Adrenergic drugs)
|
Drug or other substance that causes effects like those of the sympathetic nervous system
|
|
Sympatholytic (Antiadrenergic drugs)
|
Drug or other substance that blocks the actions of the sympathetic nervous system
|
|
Antidysrhythmic
|
Drug used to treat and prevent abnormal cardiac rhythms
|
|
Antihypertensive
|
Drug used to treat hypertension
|
|
Diuretic
|
Drug used to reduce circulating blood volume by increasing the amount of urine
|
|
Hemostasis
|
The stoppage of bleeding
|
|
Antiplatelet
|
Drug that decreases the formation of platelet plugs
|
|
Anticoagulant
|
Drug that interrupts the clotting cascade
|
|
Fibrinolytic (Thrombolytic)
|
Drug that acts directly on thrombi to break them down
|
|
Anithyperlipidemic
|
Drug used to treat high blood cholesterol
|
|
Leukotriene
|
Mediator released from mast cells upon contact with allergens
|
|
Antihistamine
|
Medication that arrests the effects of histamine by blocking its receptors
|
|
Histamine
|
An endogenous substance that affects a wide variety of organ systems
|
|
Antitussive
|
Meddication that suppresses the stimulus to cough in the central nervous system
|
|
Expectorant
|
Medication intended to increase the productivity of cough
|
|
Mucolytic
|
Medication intended to make mucus more watery
|
|
Antacid
|
Alkalotic compound used to increase the gastric environment's pH
|
|
Catergories of Laxatives
|
1. Bulk-forming
2. Stimulant 3. Osmotic 4. Surfactant |
|
Surfactant
|
Substance that decreases surface tension
|
|
Antiemetic
|
Medication used to prevent vomiting
|
|
Insulin
|
Substance that decreases blood glucose level
|
|
Glucagon
|
Substance that increases blood glucose level
|
|
Antineoplastic agent
|
Drug used to treat cancer
|
|
Antibiotic
|
Agent that kills or decreases the growth of bacteria
|
|
Pathogen
|
Disease-causing organism
|
|
Immunity
|
The body's ability to respond to the presence of a pathogen
|
|
Serum
|
Solution containing whole antibodies for a specific-pathogen
|
|
Vaccine
|
Solution containing a modified pathogen that does not actually cause disease but still stimulates the development of antibodies specific to it
|