Module 1-1 Flashcards
what are the 6 rights of medication administration?
right drug, right dose, right time, right route, right patient, right documentation
define drug
Any chemical that affects the physiologic
processes of a living organism
define pharmacology
study or science of drugs
Chemical name
Describes the drug’s chemical composition and
molecular structure
Generic name (nonproprietary name)
Name given by the United States Adopted Name
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Council
Trade name (proprietary name)
Brand name, The drug name has a registered trademark; use
of the name is restricted by the drug’s patent owner
(usually the manufacturer)
naming example:
chemical: 2-isbuphenyl blah blah
generic name: ibuprofen
trade name: Motrin
Pharmaceutics
The study of how various drug forms
influence pharmacokinetic and
pharmacodynamic activities
Pharmacokinetics
The study of what the body does to the drug Absorption Distribution Metabolism Excretion
Pharmacodynamics
The study of what the drug does to the body The mechanism of drug actions in living tissues
Pharmacotherapeutics
The use of drugs and the clinical indications
for drugs to prevent and treat diseases
Pharmacognosy
The study of natural (plant and animal) drug
sources ie. opium plant
drug abosorption-fastest to slowest
liquids elixirs and syrups, then suspension solutions, powders, capsules, tablets, coated tablets, enteric-coated tablets
Pharmacokinetics: Absorption
The rate at which a drug leaves its site of
administration, and the extent to which
absorption occurs. Includes bioavailability and bioequivalency
bioavailability
the percent of administered dose of unchanged drug that reaches systemic circulation. Impeded by complete absorption and first pass effect
bioequivalency
when two different formulations may have comparable bioavailability
Factors That Affect Absorption
Absorption characteristics vary according to
the dosage form and route:
Food or fluids administered with the drug
Dosage formulation
Status of the absorptive surface
Rate of blood flow to the small intestine
Acidity of the stomach
Status of GI motility
Routes
A drug’s route of administration affects the
rate and extent of absorption of that drug Enteral (GI tract) - easy cheap
Parenteral - fastest
Topical - slower, longer duration, more localized
Enteral route
The drug is absorbed into the systemic circulation through the oral or gastric mucosa or the small intestine Oral Sublingual Buccal Rectal
First-Pass Effect
The metabolism of a drug and its passage
from the liver into the circulation
A drug given via the oral route may be extensively metabolized by the liver before reaching the systemic circulation (high first-pass effect)
The same drug—given IV—bypasses the liver, preventing the first-pass effect from taking place, and more drug reaches the circulation
Parenteral Route
Intravenous (fastest delivery into the blood circulation) Intramuscular Subcutaneous Intradermal Intraarterial Intrathecal - into spinal column Intraarticular - into a joint
Topical Route
Skin (including transdermal patches) Eyes Ears Nose Lungs (inhalation) Rectum - half has first pass effect has does not Vagina
Distribution
The transport of a drug in the body by the
bloodstream to its site of action
Protein-binding
Water soluble vs. fat soluble - if lipid soluble it will penetrate cell membranes easier
Blood-brain barrier - small lipid soluble get through easier
Areas of rapid distribution: heart, liver,
kidneys, brain
Areas of slow distribution: muscle, skin, fat
Metabolism/Biotransformation
The biochemical transformation of a drug into an inactive metabolite, a more soluble compound, or a more potent metabolite Liver (main organ) Skeletal muscle Kidneys Lungs Plasma Intestinal mucosa