Pharmacology Chapter 2 Vocab

Additive Effects

Drug interactions in which the effect of a combination of two or more drugs with similar actions is equivalent to the sum of the individual effects of the same drugs given alone.

Adverse Drug Event

Any undesirable occurrence related to administering or failing to administer a prescribed medicaiton

Adverse drug reaction

Any unexpected, unintended, undesired, or excessive response to a medication given at therapeutic dosages

Agonist

A drug that binds to and stimulates the activity of one or more receptors in the body

Allergic Reaction

An immunologic hypersensitivity reaction resulting from the unusual sensitivity of a patient to a particular medication; a type of adverse drug event

Antagonist

A drug that binds to and inhibits the activity of one or more receptors in the body. Also called inhibitors

Antagonistic effects

Drug interactions in which the effect of a combination of two or more drugs is less that the sum of the individual effects of the same drugs given alone, it is usually caused by an antagonizing effect of one drug on another

Bioavailability

A measure of the extent of drug absorption for a given drug and route

Biotransformation

One or more biochemical reactions involving a parent drug. Biotransformation occurs mainly in the liver and produces a metabolite that is either inactive or active. Also known as metabolism

Blood-brain barrier

The barrier system that restricts the passage of various chemicals and microscopic entities between the bloodstream and the central nervous system. It still allows for the passage of essential substances such as oxygen

Chemical Name

Name that describes the chemical composition and molecular structure of a drug

Contraindication

Any condition, especially one related to a disease state or other patient characteristic, including current or recent drug therapy that renders a particular form of treatment improper or undesirable.

Cytochrome P-450

The general name fora large class of enzymes that play a significant role in drug metabolism

Dependence

A state in which there is a compulsive or chronic need, as for a drug

Dissolution

The process by which solid forms of drugs disintegrate in the GI tract and become soluble before being absorbed into the circulation

Drug

Any chemical that affects the physiologic processes of a living organism

Drug Actions

The cellular processes involved in the interaction between a drug and a body cell

Drug effects

The physiologic reactions of the body to a drug. They can be therapeutic or toxic and describe how the function of the body is affected as a whole by the drug. The terms onset, peak, and duration are used to describe drug effects

Drug induced teratogenesis

The development of congenital anomalies or defects in the developing fetus caused by toxic effects of drugs

Drug Interaction

Alteration in the pharmacologic activity of a given drug caused by the presence of one or more additional drugs; it is usually related to effects on the enzymes required for metabolism of the involved drugs.

Duration of action

Length of time the concentration of a drug in the blood or tissues is sufficient to elicit a response

Enzymes

Protein molecules that catalyze one or more of a variety of biochemical reactions, including those related to the body's own physiologic processes as well as those related to drug metabolism

First Pass Effect

The initial metabolism in the liver of a drug absorbed from the GI tract before the drug reaches systemic circulation through the bloodstream

Generic Name

The name given to a drug by the US Adopted Names Council. Also called the nonproprietary name. much shorter than the chemical name and is not protected by trademark

Half-life

In pharmocokinetics, the time required for half of an administered dose of drug to be eliminated by the body, or the time it takes for the blood level of a drug to be reduced by 50%

Idiosyncratic reaction

An abnormal and unexpected response to a medication, other than an allergic reaction, that is peculiar to an individual patient

Incompatibility

The characteristic that causes two parenteral drugs or solutions to undergo a reaction when mixed or given together that results in the chemical deterioration of at least one of the drugs

Intraarticular

Within a joint

Intrathecal

Within a sheath ( theca of the spinal cord)

Medication Error

Any preventable adverse drug event involving inappropriate medication use by a patient or health care professional; it may or may not cause patient harm

Medication use Process

The prescribing, dispensing, and administering of medications, and the monitoring of their effects.

Metabolites

A chemical form of a drug that is the product of one or more biochemical reactions involving the parent drug. Active metabolites are those that have pharmacologic activity of their owns, even in the parent drug is inactive. Inactive metabolites lack pharm

Onset of Action

Time required for a drug to elicit a therapeutic response after dosing

Parent Drug

Chemical form of a drug that is administered before iti is metabolized by the body's biochemical reactions into its active or inactive metabolites. A parent drug that is not pharmacologically active itself is called a produrg. A prodrug is then metabolize

Peak effect

Time required fora drug to reach its maximum therapeutic response in the body

Peak Level

The maximum concentration of a drug in the body after administration, usually measure in the blood sample for therapeutic drug monitoring

Pharmaceutics

Science of preparing and dispensing drugs, including dosage form design.

Pharmacodynamics

The study of the biochemical and physiologic interactions of drugs at their sties of activity. It examines the physiochemical properties of drugs and their pharmacologic interactions with body receptors

Pharmacogenetics

Study of the influence of genetic factors on drug response, including the nature of genetic aberrations that result in the absence, overabundance, or insufficiency of drug metabolizing enzymes

Pharmacognosy

The study of drugs that are obtained from natural plant and animal sources

Pharmacokinetics

The rate of drug distribution among various body compartments after a drug has entered the body. It includes the phases of absorption, distribution, metabolism, and excretion of drugs.

Pharmacology

Broadest term for the study of science of drugs

Prodrug

An inactive drug dosage form that is converted to an active metabolite by various biochemical reactions once it is inside the body

Receptor

A molecular structure within or on the outer surface of a cell. Receptors bind specific substances and one or more corresponding cellular effects as a result of this drug-receptor interaction

Steady State

Physiologic state in which the amount of drug removed via elimination is equal to the amount of drug absorbed with each dose

Substrates

Substances on which an enzyme acts

Synergistic effects

Drug interactions in which the effect of a combination of two or more drugs with similar actions is greater than the sum of the individual effects of the same drugs given alone.

Therapeutic drug Monitoring

The process of measuring drug peak and trough levels to gauge the level of a patient's drug exposure and allow adjustment of dosages with the goals of maximizing therapeutic effects and minimizing toxicity

Therapeutic Effect

Desired or intended effect of a particular medication

Therapeutic Index

Ratio between the toxic and therapeutic concentrations of a drug

Tolerance

Reduced response to a drug after prolonged use

Toxic

Quality of being poisonous

Toxicity

Condition of producing adverse bodily effects due to poisonous qualities

Toxicology

Study of poisons, including toxic drug effects, and applicable treatments

Trade Name

Commerical name given to a drug product by its manufacturers also called the proprietary name

Trough Level

Lowest concentration of drug reached int he body after it falls from its peak level, usually measure in a bloods sample for therapeutic drug monitoring