Pharmaceutics - ANSWER the dosage form that determines the rate of drug dissolution
Pharmacodynamics - ANSWER - what the drug does to the body
- therapeutic effects
Selective Enzyme Interaction - ANSWER when the drug binds to an enzyme molecule
and inhibits (blocks) or stimulates the enzyme action with the normal target cell
Pharmacokinetics - ANSWER - what the body does to the drug
- study of movement of drugs throughout the body
Absorption - ANSWER being absorbed or used by the tissues
Fastest to Slowest Absorption Routes by Mouth - ANSWER - Sublingual
- Liquid Suspension
- Capsule
- Tablet
- Enteric Coated Tablet
- Extended Release Tablet
First Pass Effect - ANSWER oral doses of drugs are absorbed into the GI tract and
metabolized by the liver, resulting in a reduced amount of bioavailability or active drug in
the circulatory system.
*Oral doses are generally higher to allow for this effect*
Drugs that are Effected by First Pass Effect - ANSWER - Elixir
- Tablets
- Capsules
*enteral drugs*
What drugs aren't effected by First Pass Effect? - ANSWER - IV
- Sublingual
- Transdermal Patch
- Suppository
*parenteral drugs*
Half Life - ANSWER - the time t takes for 1/2 of the drug dose to be eliminated from the
body
-drugs with a long half life enables them to be taken less frequently
EX: ibuprofen has a half life of 2 hours, after 1 half life 200 mg will turn into 100 mg
Plasma - ANSWER yellow fluid part of blood that holds the cells
Interstitial Fluid - ANSWER fluid within the cells
, NR 293 - Exam 1
Transcellular Fluid - ANSWER part of extracellular fluid
Areas of Fast Distribution - ANSWER - Heart
- Liver
Areas of Slow Distribution - ANSWER - Muscle
- Fat
- Skin
Protein Binding Complications - ANSWER if a person has a low protein , or albumin
level, free drug will be circulating and can cause toxicity of the drug.
EX: a person with normal albumin levels is prescribed more than one drug that is highly
protein binding. the prescriber will likely decrease the dose of both drugs to avoid drug
toxicity
Normal Albumin Level - ANSWER 3.5-5.5 g/dL
Metabolism - ANSWER use and transformation of drugs so that they can be excreted
from the body
Where are most drugs metabolized/excreted? - ANSWER - Liver
- Kidney
Neonates/Infants: Drug Metabolism - ANSWER have immature liver and kidneys
causing them to have decreased or poor metabolism and excretion of drugs
Cytochrome P-450 - ANSWER when drugs are bio-transformed through an enzyme to
form fat-soluble metabolites that are easy to eliminate
Liver Failure: Drug Metabolism - ANSWER have difficulty metabolizing certain drugs
Fast/Slow Acetylators - ANSWER genetic conditions that affect how the liver
metabolizes drugs
Excretion - ANSWER drugs excreted through liver, kidneys (urine), hair, skin, breath,
saliva, perspiration, feces, milk and bile
Six Rights of Medication Administration - ANSWER - Right Patient
- Right Drug
- Right Route
- Right Dose
- Right Time
- Right Documentation