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Study of biological effects of chemicals |
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Chemicals that are introduced into the body to bring about some sort of change. |
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Drug effects that are not the desired therapeutic effects; may be unpleasant or even dangerous! |
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name given to drug by the pharmaceutical company that developed it; also called TRADE NAME |
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name that reflects the chemical
structure of a drug |
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drugs sold by their chemical names; not brand or trade names products. |
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the original name that a drug is given when the drug company that developed it applies for the approval process. |
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drugs that have been discovered but would not be profitable for development;usually treat only small #of people; can be adopted by drug companies to develop. |
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clinical pharmacology- the branch that deals w/drugs; chemicals that are used in medicine for the treatment,prevention,and diagnosis of disease in humans.
*NURSES
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pilot study-potential drug done w/small #of selected,healthy human volunteers |
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clinical study-of proposed drug by selected physicians using actual patients who have disorder drug designed to treat; patients must provide informed consent |
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Use of Proposed Drug on wide scale- in clinical setting w/patients who have disease drug is thought to treat |
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continual evaluation-of drug after it has been released for marketing |
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initial trial of a chemical thought to have therapeutic potential; uses laboratory animals, not human subjects
1) to determine whether they have effects in human tissue
2) evaluate any adverse effects |
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having adverse effects on the fetus |
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plants-
animals- used to replace human chemicals (pancreas of cow/insulin)
inorganic compounds- fluoride,iron
synthetic sources- alter bacteria to produce chemicals more useful |
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drugs that interact directly w/receptor sites to cause same activity natural chemical would. |
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2 key concerns w/Clinical Pharmacology |
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*drugs effects on the body
*body's response to the drug |
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(AAA-TE)
*Assessment
*Administer drugs
*Assesment of reaction/outcome to med's
*Teaching
*Evaluation of teaching effectiveness |
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React with receptor sites to block normal stimulation; producing no effect. |
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non-competitive
antagonist |
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React w/specific receptor sites on cell and, by reacting there, prevent reaction of another chemical w/different receptor site on that cell. |
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groups of similar drugs derived from an original prototype, each one in group slightly different depending on desired situation of treatment. |
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Why chemicals are discarded- |
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(TTS)
*Chemical too toxic
*Highly teratogenic
*Safety margins too small & chemical not useful in clinical setting |
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Adequate studies provide no risk to fetus in any trimester |
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Animal studies give no risk fetus but; no adequate studies in pregnant woman. (Studies that have been done show no risk in any trimester) |
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Animal studies show adverse effect on fetus; no adequate study in humans. (Drug benefits may be worth risk) |
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Evidence of human fetal risk. (Drug benefits may be worth risk.) |
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Studies in animals or humans demonstrate fetal abnormalities or adverse reactions; Risk clearly outweighs use & possible benefits...don't do it. |
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high abuse potential
(heroin;LSD) |
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high abuse potential w/dependence liability
(amphetamines;barbituates) |
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Less abuse potential than 2-moderate dependence liability
(nonbarbituate sedatives;nonamphetamine stimulants) |
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Less abuse potential than 3- limited dependence liability
(some sedatives;antianxiety;non-narcotic analgesics) |
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Limited abuse potential; primarily small amounts of narcotics that can be purchased OTC
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science that deals with the interactions between chemical compounds of living systems & foreign chemicals;
THE WAY THE DRUG AFFECTS THE BODY! |
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How the body acts on the drug!
-Dosing needs to be correct
-Loading Dose given
-Dynamic Equilibrium considered |
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(RIID)
*Replace missing chemicals
*Increase/stimulate cellular activity
*Interfere w/functioning foreign cells
*Depress/slow cellular activities |
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Actual amount of drug that reaches body
Affected by= Absorbtion Distribution
Biotransformation Excretion
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Med's extensively absorbed by liver
Most drug takes path of
sm.intestines portal vein liver
*Oral drugs in higher dose due to 1st pass effect! |
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Definition
*All drugs are protein bound
-Not active yet
-Must be lipid soluble to cross Blood Brain Barrier
-Most drug are not BBB & don't have
direct effect on CNS
-Liver uses enzyme P450 to start biotransfer |
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(MADE)
How long to decrease to 1/2 peak level
Affected by: Absorption,Distribution,
Metabolism, & Excretion |
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Anaphylactic - Hives/Rash/Closes Airway
Cytotoxic- Cause cell damage..Low White Blood Count
Serum Sickness- Damage to tissue..swollen joints
Delayed Reaction- Swollen joints |
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Assessment - History/Physically Assess
Diagnosis- Draw conclusion from data
Intervention- Formulate plan .... action/improve/maintain PT health----
Evaluation- Is plan effective for PT? |
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DD plays rag time daily profusely!
Drug/Dose/Prep/Route/
Time/Document/PT |
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-Chemicals that inhibit specific bacteria
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-Substances that prevent
the growth of bacteria |
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-Substances that kill
bacteria directly |
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- Based on Culture Report, antibiotic chosen that is known to be effective treatment of invading organism |
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Viruses that respond
to Antiviral Agents |
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Definition
-Influenza A
-Some Respitory Viruses
-CMV (Cytomegalovirus)
-HIV / AIDS
-Some Viruses that cause Warts/Eye Infections
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Definition
-Influenza A
-Influenza B
-RSV |
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-May be asymptomatic
-Fatigue
-Mausea
-Jaundice
-Still birth or defects/brain damage |
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-Painful vesicles in clusters....
skin/cornea/mucous membranes
-Usual course of primary disease 2wks.
-Duration of recurrences varies |
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-Drugs designed to act on foreign organisms that have infected the host with selective toxicity.
(Invade the organism...not hosts good cells) |
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