Vocabulary Flashcards

1
Q

Absorption

A

Process by which a drug enters the circulatory system.

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2
Q

The Pharmacokinetic Processes

A

Absorption, Distribution, Metabolism, and Elimination (ADME)

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3
Q

Addiction

A

Dependence characterized by a received need to take a drug to attain the psychological and physical effects of mood altering substances.

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4
Q

Affinity

A

Natural attraction; the strength by which a particular chemical messenger binds to its receptor site on a cell.

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5
Q

Agonist

A

Drug that mimics the action of a neurotransmitter when it binds to a particular receptor site - i.e. & triggers the cell’s response in a manner similar to the action of the body’s own chemical messenger.

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6
Q

Anaphylactic Reaction

A

Severe allergic response resulting in immediate life-threatening respiratory distress, usually followed by vascular collapse & shock accompanied w/ hives.

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7
Q

Angiodema

A

Abnormal accumulation of fluid in tissue.

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8
Q

Antagonist

A

Drug that neutralizes or counteracts the effects of a neurotransmitter or another drug when it binds to a particular receptor site.

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9
Q

Antigen

A

Foreign substance that is recognized by the immune system & induces the immune system to produce antibodies to defend against the foreign substance.

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10
Q

Bioavalibility

A

Degree to which a drug or other substance becomes available to the target tissue after administration.

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11
Q

Blood-Brain Barrier

A

Fortified area that prevents many substances from entering the cerebro-spinal fluid from the blood. This area is formed by glial cells that envelope capillaries in the fcentral nervous system. This creates a shield that blocks many water-soluble compounds, but is permeable to lipid-soluble substances.

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12
Q

Ceiling Effect

A

Point @ which no clinical response occurs w/ increased dosage of a drug.

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13
Q

Clearance

A

Rate @ which a drug is eliminated from a specific volume of blood per unit of time.

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14
Q

Contraindication

A

Any disease, condition, or symptom for which a drug will not be beneficial & may be harmful.

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15
Q

Body Molecules drugs ca combine with:

A

Enzymes, Nucleic Acids, Receptors, Transport Proteins

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16
Q

Duration of Action

A

Length of time a drug gives the desired response/remains at the therapeutic level.

17
Q

Elimination

A

Removal of a drug or the drugs metabolites from the body by excretion.

18
Q

First-Order

A

Drugs for which the rate of elimination is concentration dependent

19
Q

First Pass Effect

A

Extent to which a drug is metabolized by the liver before reaching full body circulation. This can substantially decrease bioavailability of certain drugs when administered orally, in which case administration by injection is required.

20
Q

Half-Life

A

Time necessary for the body to eliminate half of the drug in the body @ any 1 time (written as T 1/2).

21
Q

Induction

A

Process by which a drug increases the concentration of certain enzymes that affect the pharmacologic response to other drugs.

22
Q

Inhibition

A

Process by which a drug blocks enzyme activity & impairs the metabolism of another drug.

23
Q

Loading Dose

A

Amt of a drug that will bring the blood concentration rapidly to a therapeutic level.

24
Q

Maintinance Dose

A

Amt of a drug administered at regular intervals to keep the blood concentration @ a therapeutic level. An important factor in determining this, is a drug’s clearance rate.

25
Q

Peak

A

Top or upper limit of a drug’s concentration in the blood.

26
Q

Pharmacokinetic Modeling

A

Method of describing the process of absorption, distribution, metabolism, & elimination (ADME) of drug w/i the body mathematically.

27
Q

Prophylaxis

A

Effect of a drug in preventing infection or disease.

28
Q

Pruritis

A

Itching Sensation.

29
Q

Specicifity

A

Property of a cell receptor that enables it to bind only w/ a specific chemical messenger complementary to the structure of the receptor.

30
Q

Trough

A

Lowest level of a drug in the blood.

31
Q

Wheals

A

Slightly elevated, red areas on the surface of the body.

32
Q

Zero-Order

A

Drugs for which the rate of elimination is not concentration dependent

33
Q

Blinded Investigational Drug Study

A

A research design in which the subjects are purposely unaware of whether the substance they are administered is the drug under study or the placebo. This method serves to eliminate bias on the part of research subjects in reporting their body’s responses to investigational drugs.

34
Q

Double-blind Investigational Drug Study

A

A research design in which both of the investigator(s) and the subjects are purposely unaware of whether the substance administered to a given subject is the drug under study or the placebo. This method eliminates bias on the part of both investigator and the subject.

35
Q

Drug Polymorphism

A

Variation in response to a drug because of a patient’s age, gender, size, and/or body composition.

36
Q

Expeditated Drug Approval

A

Acceleration of the usual investigational new drug approval process by the U.S. Food and Drug Administration (FDA) and pharmaceutical companies, usually for drugs used to treat life-threatening diseases.

37
Q

Invesigational New Drug

A

A drug not approved for marketing by the FDA but available for use in experiments to determine its safety and efficacy

38
Q

Narcotic

A

Applied to drugs that produced insensibility or stupor, especially the opioids (e.g., morphine, heroin). The term is currently used in clinical settings to refer to and medically administered controlled substance and in legal settings to refer to any illicit or “street” drug.

39
Q

Orphan Drugs

A

Drugs for rare diseases