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adverse effects
drug effects, sometimes called side effects, that are not the desired therapeutic effects; may be unpleasant or even dangerous
brand name
name given to a drug by the pharmaceutical company that developed it; also called a trade name or proprietary name
chemical name
name that reflects the chemical structure of a drug
drugs
chemicals that are introduced into the body to bring about change
Food and Drug Administration (FDA)
federal agency responsible for the regulation and enforcement of drug evaluation and distribution policies
generic drugs
drugs sold by their generic name; not brand name or trade name product
generic name
the original designation that a drug is given when the drug company that developed it applies for the approval process
genetic engineering
process of altering DNA, usually of bacteria, to produce a chemical to be used as a drug
orphan drugs
drugs that have been discovered but would not be profitable for a drug company to develop; usually drugs that would treat only a small number of people; these orphans can be adopted by drug companies to develop
over-the-counter (OTC) drugs
drugs that are available without a prescription for self-treatment of a variety of complaints; deemed to be safe when used as directed; often formerly only available by prescription
pharmacology
the study of the biological effects of chemicals
pharmacotherapeutics
clinical pharmacology—the branch of pharmacology that deals with drugs; chemicals that are used in medicine for the treatment, prevention, and diagnosis of disease in humans
phase I study
a pilot study of a potential drug using a small number of selected, usually healthy human volunteers
phase II study
a clinical study of a proposed drug by selected physicians using actual patients who have the disorder the drug is designed to treat; patients must provide informed consent
phase III study
use of a proposed drug on a wide scale in the clinical setting with patients who have the disease the drug is thought to treat
phase IV study
continuous evaluation of a drug after it has been released for marketing
preclinical trials
initial trial of a chemical thought to have therapeutic potential; uses laboratory animals, not human subjects
teratogenic
having adverse effects on the fetus
absorption
what happens to a drug from the time it enters the body until it enters the circulating fluid; intravenous administration causes the drug to directly enter the circulating blood, bypassing the many complications of absorption from other routes
active transport
the movement of substances across a cell membrane against the concentration gradient; this process requires the use of energy
chemotherapeutic agents
synthetic chemicals used to interfere with the functioning of foreign cell populations, causing cell death; this term is frequently used to refer to the drug therapy of neoplasms, but it also refers to drug therapy affecting any foreign cell
critical concentration
the concentration a drug must reach in the tissues that respond to the particular drug to cause the desired therapeutic effect
distribution
movement of a drug to body tissues; the places where a drug may be distributed depend on the drug's solubility, perfusion of the area, cardiac output, and binding of the drug to plasma proteins
enzyme induction
process by which the presence of a chemical that is biotransformed by a particular enzyme system in the liver causes increased activity of that enzyme system
excretion
removal of a drug from the body; primarily occurs in the kidneys, but can also occur through the skin, lungs, bile, or feces
first-pass effect
a phenomenon in which drugs given orally are carried directly to the liver
First-pass effect
Phenomenon in which drugs given orally are carried directly to the liver after absorption, where they may be largely inactivated by liver enzymes before they can enter the general circulation.
Glomerular filtration
The passage of water and water-soluble components from the plasma into the renal tubule.
Half-life
The time it takes for the amount of drug in the body to decrease to one half of the peak level it previously achieved.
Hepatic microsomal system
Liver enzymes tightly packed together in the hepatic intracellular structure, responsible for the biotransformation of chemicals, including drugs.
Loading dose
Use of a higher dose than what is usually used for treatment to allow the drug to reach the critical concentration sooner.
Passive diffusion
Movement of substances across a semipermeable membrane with the concentration gradient; this process does not require energy.
Pharmacodynamics
The study of the interactions between the chemical components of living systems and the foreign chemicals, including drugs, that enter living organisms; the way a drug affects a body.
Pharmacogenomics
The study of genetically determined variations in the response to drugs.
Pharmacokinetics
The way the body deals with a drug, including absorption, distribution, biotransformation, and excretion.
Placebo effect
Documented effect of the mind on drug therapy; if a person perceives that a drug will be effective, the drug is much more likely to actually be effective.
Receptor sites
Specific areas on cell membranes that react with certain chemicals to cause an effect within the cell.
Selective toxicity
Property of a chemotherapeutic agent that affects only systems found in foreign cells without affecting healthy human cells.
Blood dyscrasia
Bone marrow depression caused by drug effects on the rapidly multiplying cells of the bone marrow; lower-than-normal levels of blood components can be seen.
Dermatological reactions
Skin reactions commonly seen as adverse effects of drugs; can range from simple rash to potentially fatal exfoliative dermatitis.
Drug allergy
Formation of antibodies to a drug or drug protein; causes an immune response when the person is next exposed to that drug.
Hypersensitivity
Excessive responsiveness to either the primary or the secondary effects of a drug; may be caused by a pathological condition or, in the absence of one, by a particular patient's individual response.
Poisoning
Overdose of a drug that causes damage to multiple body systems and has the potential for fatal reactions.
Stomatitis
Inflammation of the mucous membranes related to drug effects; can lead to alterations in nutrition and dental problems.
Superinfections
Infections caused by the destruction of normal flora bacteria by certain drugs, which allow other bacteria to grow out of control and cause infection.
Alternative therapy
Includes herbs and other 'natural' products as often found in ancient records; these products are not controlled or tested by the U.S. Food and Drug Administration and are considered to be dietary supplements.
Biological weapons
So-called germ warfare; the use of bacteria, viruses, and parasites on a large scale to incapacitate or destroy a population.
Cost comparison
A comparison of the relative cost of the same drug provided by different manufacturers to determine the costs.
off-label uses
uses of a drug that are not part of the stated therapeutic indications for which the drug was approved by the FDA; off-label uses may lead to new indications for a drug
self-care
patients self-diagnosing and determining their own treatment needs
street drugs
nonprescription drugs with no known therapeutic use; used to enhance mood or increase pleasure
actin
thin filament, a component of a sarcomere, or muscle unit
aldosterone
a hormone released from the adrenal cortex that acts in the distal convoluted tubule of the kidney to increase retention of sodium and water
angiotensin
a peptide hormone that causes vasoconstriction and stimulates aldosterone and ADH release; part of the renin-angiotensin system
antidiuretic hormone (ADH)
released from the posterior pituitary and acts in the distal convoluted tubule of the kidney to increase water retention
arrhythmia
a disruption in cardiac rate or rhythm, also called dysrhythmia
arteries
vessels that take blood away from the heart; muscular, resistance vessels
atrium
top chamber of the heart, receives blood from veins
auricle
appendage on the atria of the heart, holds blood to be pumped out with atrial contraction
automaticity
property of heart cells to generate an action potential without an external stimulus
capacitance system
the venous system; distensible, flexible veins that are capable of holding large amounts of blood
capillary
small vessel made up of loosely connected endothelial cells that connect arteries to veins
cardiac cycle
a period of cardiac muscle relaxation (diastole) followed by a period of contraction (systole) in the heart
conductivity
property of heart cells to rapidly conduct an action potential of electrical impulse
diastole
resting phase of the heart; blood is returned to the heart during this phase
dysrhythmia
a disruption in cardiac rate or rhythm, also called an arrhythmia
ectopic focus
a shift in the pacemaker of the heart from the sinoatrial node to some other site
electrocardiogram
an electrical tracing reflecting the conduction of an electrical impulse through the heart muscle; does not reflect mechanical activity
myocardium
the muscle of the heart
myosin
thick filament with projections, a component of a sarcomere, or muscle unit
natriuretic peptide
a peptide produced by the brain, heart, and vasculature, which causes natriuresis, excretion of sodium in the urine; degraded by the enzyme neprilysin
oncotic pressure
the pulling pressure of the plasma proteins, responsible for returning fluid to the vascular system at the capillary level
pulse pressure
the systolic blood pressure minus the diastolic blood pressure; reflects the filling pressure of the coronary arteries
resistance system
the arteries; the muscles of the arteries provide resistance to the flow of blood, leading to control of blood pressure
sarcomere
functional unit of a muscle cell, composed of actin and myosin molecules arranged in layers to give the unit a striped or striated appearance
sinoatrial (SA) node
the normal pacemaker of the heart; composed of primitive cells that constantly generate an action potential
Starling's law of the heart
addresses the contractile properties of the heart: the more the muscle is stretched, the stronger it will react until it is stretched to a point at which it will not react at all
systole
contracting phase of the heart, during which blood is pumped out of the heart
troponin
chemical in heart muscle that prevents the reaction between actin and myosin, leading to muscle relaxation; it is inactivated by calcium during muscle stimulation to allow actin and myosin to react, causing muscle contraction
myosin
a protein that interacts with actin to cause muscle contraction
veins
vessels that return blood to the heart; distensible tubes
ventricle
bottom chamber of the heart, which contracts to pump blood out of the heart
angiotensin-converting enzyme (ACE) inhibitor
drug that blocks ACE, the enzyme responsible for converting angiotensin I to angiotensin II in the lungs; this blocking prevents the vasoconstriction and aldosterone release related to angiotensin II
angiotensin II receptors
specific receptors found in blood vessels and in the adrenal gland that react with angiotensin II to cause vasoconstriction and release of aldosterone
baroreceptor
pressure receptor; located in the arch of the aorta and in the carotid artery; responds to changes in pressure and influences the medulla to stimulate the sympathetic system to increase or decrease blood pressure
cardiovascular center
area of the medulla at which stimulation will activate the sympathetic nervous system to increase blood pressure and heart rate
essential hypertension
sustained blood pressure above normal limits with no discernible underlying cause
hypotension
sustained blood pressure that is lower than that required to adequately perfuse all of the body's tissues
peripheral resistance
force that resists the flow of blood through the vessels, mostly determined by the arterioles, which contract to increase resistance; important in determining overall blood pressure
renin-angiotensin-aldosterone system
compensatory process that leads to increased blood pressure and blood volume to ensure perfusion of the kidneys; important in the continual regulation of blood pressure
shock
severe hypotension that can lead to accumulation of waste products and cell death
stroke volume
the amount of blood pumped out of the ventricle with each beat; important in determining blood pressure
antihyperlipidemic agents
general term used for drugs used to lower lipid levels in the blood
bile acids
cholesterol-containing acids found in the bile that act like detergents to break up fats in the small intestine
cholesterol
necessary component of human cells that is produced and processed in the liver and then stored in the bile until stimulus causes the gallbladder to contract and send the bile into the duodenum via the common bile duct; a fat that is essential for the formation of steroid hormones and cell membranes; it is produced in cells and taken in by dietary sources
chylomicron
carrier for lipids in the bloodstream, consisting of proteins, lipids, cholesterol, and so forth
high-density lipoprotein (HDL)
loosely packed chylomicron-containing fats, able to absorb fats and fat remnants in the periphery; thought to have a protective effect, decreasing the development of coronary artery disease
hydroxymethylglutaryl-coenzyme A (HMG-CoA) reductase
enzyme that regulates the last step in cellular cholesterol synthesis
hyperlipidemia
increased levels of lipids in the serum, associated with increased risk of coronary artery disease development
low-density lipoprotein (LDL)
tightly packed fats that are thought to contribute to the development of coronary artery disease when remnants left over from the LDL are processed in the arterial lining