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18 Cards in this Set

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Pharmacokinetics definition
The study of drug movement throughout the body. In relation to absorption, distribution, metabolism and secretion.
mechanics
Absorption
movement from site of administration, across membranes, into bloodstream. It determines when drug becomes available to exert its action.
Factors affecting absorption
Route (IV is fastest, then other liquids)
Drug formulation and solubility
Drug dosage
Blood flow
Conditions at the site administration
Effects of pH
Drug drug/drug-food interactions
Distribution
3 factors affect distribution
1) local blood flow
2) membrane permeability
3) protein- binding capacity
Protein binding
A drug can be freely distributed only if NOT bound to a protein.
Drug circulates in body until it is released or displaced.
Metabolism (Biotransformation)
chemically converting a drug to a form more easily removed by the body.

Liver is the primary site.
Factors that affect metabolism
Liver function and the first-pass effect
First-pass effect
Drug absorbed, enters hepatic circulation, metabolized to inactive form, conjugates and leaves liver, distributed to general circulation.
Excretion
Elimination of drugs.
Primary site is the kidneys.
also, liver and GI tract, lungs, exocrine glands.
Onset
Time it takes for a drug to ellicit a response
Peak
Time it takes for the drug to reach its maximum response in the body.
Duration
Length of time that a drug concentration in the blood or tissues is sufficient to ellicit a therapeutic response.
Pharmacodynamics definition
How medications achieve their effects in the body. How a medicine changes the body.
Common side effects (usually predictable)
N/V/D
Dizziness
Drowsiness
Dry mouth
Abdominal distention/distress
Constipation
Toxicity
dangerous and damaging effects to an organ or tissue.
usually localized
Caused by:
overdose
accumulation
abnormal sensitivity
Allergic reaction S/Sx
Urticaria (hives)
Pruritus (itching)
Edema
Rhinitis
Respiratory distress
Tetrogenesis
a drugs ability to cause permanent abnormality or death of a fetus.
Category A- safe for fetus
Category B- no harm but not enough studies.
Category C- adverse effect
Category D- risk to fetus
Category X- cause fetal abnormalities or death.
Medication interactions
Antagonistic-one drug decreases the effects of the other.
Synergistic- one drug increases the effects of the other.
Incompatibilities- multiple drugs mixed together causes chemical deterioration.