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Pharmacology Chap 2

Pharmacokinetics and factors of Individual Variation

QuestionAnswer
Bioavailability The percentage of the drug dosage that is absorbed
drug absorption entrance of a drug into the bloodstream from its site of administration
drug addiction condition of drug abuse and drug dependence that is characterized by compulsive drug behavior
drug dependence condition of reliance on the use of a particular drug characterized as physical and/or psychological dependence
drug distribution passage of a drug from the blood to the tissues and organs of the body
drug excretion elimination of the drug from the body
drug metabolism(biotransformation) chemical alteration of drugs and foreign compounds in the body.
Drug microsomal metabolizing system (DMMS) group of enzymes in the liver that specifically function to metabolize foreign drug substances
Drug tolerance decreased drug effect occurring after repeated drug administration.
enzyme induction increase in the amount of drug-metabolizing enzymes after repeated administration of certain drugs.
enzyme inhibition inhibition of drug-metabolizing enzymes by certain drugs.
first-pass metabolism drug metabolism that occurs in the intestines and liver during oral absorption of drug in to the systemic circulation
half-life time required for the body to reduce the amount of drug in the plasma by one-half.
individual variation difference in the effects of drugs and drug dosages from one person to another.
intramuscular (IM) injection route of drug administration; drug is injected into glteal or deltoid muscles.
intravenous (IV) injection route of drug administration; drug is injected directly into a vein.
loading dose initial drug does administered to rapidly achieve therapeutic drug concentrations
maintenance dose dose administered to maintain drug blood levels in the therapeutic range
oral administration (30 to 60 minute onset of action) route of drug administration by way of the mouth through swallowing
parenteral administration route of drug administration that does not involve the gastrointestinal (GI) tract
pharmacokinetics describes the processes of drug absorption, distribution, metabolism, and drug excretion
What determines what from a drug will be administered The physical and chemical properties of a drug
Syrup(Aqueous Preparation) Solution of water and sugar to which a drug is added
What are the name of several drugs dissolved in alcohol Elixirs, spirits, tinctures, and fluid extracts
Powders drug extracts that are dried and ground into fine particles
Tablets drug powders compressed into a convenient form for swallowing.
Troches and lozenges Flattened tables that are allowed to dissolve in the mouth.
Gelatin capsules used to administer drug powders or liquids
Delayed-Release Products Various portions of the drug dissolve at different rates
enteric-coated products drug tablet or capsule coated with an acid-resistant substance that will dissolve only in the less acidic portions of the intestine
Suppositories intended for insertion into the rectum, urethra, or vagina
Ointments(Petrolatum or Lanolin) Soft, oily substance containing a drug that is applied to the skin.
Transdermal Products Drug is released from a bandage or patch and is then absorbed through the skin into systemic circulation
Parenteral injection involves the administration of drugs by needle and syringe
Parenteral Administration Any route that does not involve the GI tract, including inhalation, hypodermic injection, and topical application.
What are the most common routes of parenteral administration Intramuscular (IM) injection, intravenous (IV) injection, inhalation, and topical application.
IM injections delivered into the gluteal or deltoid muscles.
Intravenous injection Fastest means of drug absorption
Inhalation involves the administration of drugs through the nose or mouth and into the lungs during respiratory inspiration
Topical application Creams and ointments used for local effects.
Drug Absorption Entrance of a drug into the bloodstream.
What special transport mechanisms do cells have that allow various substances to pass through the cell membrane filtration, passive transport, and active transport
Passive transport drug molecules diffuse from an area of high concentration to an area of low concentration
Lipid Solubility Drug that is liquid soluble passes through a lipid substance faster
Acid drug ionized in alkaline urine
basic drugs ionized in acid urine
enteroheptic pathway liver-> bile->intestines->blood-> liver
Respiratory excretion drugs metabolized to products that can be exchanged from blood into the respiratory tract.
Placebo effect The influence of one's mined on the course of treat
Drug Compliance Taking a drug exactly as prescribed
Created by: Mickensg
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