Term
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Definition
Chemical name
Generic name
Official name
Trade or brand name
(Best to use generic name to avoid confusion) |
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Definition
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Trade name for Acetominophen |
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Definition
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Definition
Therapeutic & Pharmacologic
Classified by chemical type,active ingredient, what they are used for (purpose)
Can be in one or more classes
Examples:antiinfectives,diuretics,laxatives,Anti-diabetic,Anti-neoplastic. |
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Term
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Definition
Prescription (legend drugs)
Nonprescription (over the counter(OTC))
Controlled substance-Carefully monitored b/c they can be abused & cause physical or psychological dependency. |
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Controlled Substance Act of 1970 |
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Definition
Regulates the manufacture, distribution, and dispensing of drugs that have abuse potential. |
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Schedule of controlled substances |
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Definition
Drugs divided into 5 schedules, (based on their potential for abuse and physical and psychological dependence)(I,II,III,IV,V) |
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Term
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Definition
High abuse potential
Lack of accepted safety, not approved for medical use in the U.S.
Examples: heroin, marijuana, ecstacy, peyote. |
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Term
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Definition
Potential for high abuse with severe physical or psychological dependence.
Approved for medical use in the U.S.
Examples: Opiods such as meperidine, mathadone, morphine, oxycodone, amphetamines and cocaine. |
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Term
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Definition
Less abuse potential than schedule II drugs.
Potential for moderate physical or psychological dependence.
Examples: Anabolic steroids, ketamine, hydrocodone/codeine compounded with a nonsteroidal anti-inflammatory drug. |
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Term
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Definition
Less abuse potential than schedule III drugs.
Limited dependence potential.
Examples: Some sedatives and anxiety agents, non-opioid analgesics, "diet drugs" |
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Term
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Definition
Limited abuse potential
Examples: Small amounts of opioid (codeine) used as antitussive or antidiarrheals, pregabalin (Lyrica) |
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Term
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Definition
Must be written in ink
Must include name and address of patient and DEA number of the healthcare provider.
Can't be filled more than 6 months after written.
Cant be refilled more than 5 times. |
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Term
In hospitals, nursing homes/other agencies, narcotic counts must be done how often? |
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Definition
8-12 hours
to account for every ampule, tablet, vial or other form of controlled drug. |
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Term
How long is the process of drug development? |
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Definition
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Term
Act passed to encourage development and marketing for rare diseases? |
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Definition
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Term
Dissolution(dissolving) of drug occurs; drug must be soluble to be absorbed. |
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Definition
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Term
Absorption; distribution; metabolism; excretion |
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Definition
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Term
The drugs action/effect on the body. |
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Definition
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Term
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Definition
Liquid and parenteral drugs: Already dissolved-quickly absorbed.
Solid forms of drugs: Tablets or capsules-Disintegrate into small particles; dissolve into bodyfluids in GI tract.
Enteric-coated tablets don't disintegrate until they reach the alkaline environment of the small intestine. |
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Term
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Definition
Activities within the body after the drug has been administered.
Absorption-Half-life
Distibution-Onset, Peak, & Duration(important with insulin)
Metabolism
Excretion
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Term
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Definition
Drug particles within the GI tract are moved into body fluids. |
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Term
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Definition
Drug is absorbed by the small intestine; liver first metabolizes drug; amount of drug remaining may not be sufficient to produce therapeutic effect, as a result the patient needs higher dosage for desired effect. |
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Term
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Definition
Body changes drug to a more or less active form of excretion-called metabolites. |
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Term
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Definition
Elimination of drugs from the body. |
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Term
Patients with kidney disease |
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Definition
Require dosage reduction and careful monitoring of kidney function. |
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Term
Why should older adults and children have careful monitoring and lower dosages of meds. |
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Definition
Due to diminished kidney function in the older adult and immature kidney function in children.
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Term
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Definition
Time required for the body to eliminate 50% of the drug.
Important when deciding dosage and frequency of the drug.
Drugs with short half-life(2-4 hours are administered frequently (aspirin for example)
Drugs with long half-life (21-24 hours) require less frequent dosing (Digoxin for ex. has a 36 hour half-life) |
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Definition
Time between drug administration and beginning of therapeutic effect. |
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Definition
Absorption rate equals elimination rate (not always the time of peak response.) |
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Definition
Length of time drug needs to produce a therapeutic effect. |
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Term
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Definition
Study of drugs action and effect in the body, interaction between drugs and their receptors. |
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Term
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Definition
Desired or therapeutic effect. |
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Term
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Definition
Other desirable or undesirable effects. |
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Term
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Definition
Binds with and stimulates the receptor and produces a therapeutic response. |
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Definition
It joins with but does not stimulate receptors; blocks the receptors function. |
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Physically altered environment |
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Definition
pressures, lubrication, absorption, and other conditions of the cell membrane are changed. |
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Term
Chemically altered environment |
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Definition
Alterations of chemical components of body fluids, such as changes in pH caused by antacids.
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Term
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Definition
Creation of individualized drug therapy that allows for the best choice and dose of drugs. |
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Term
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Definition
Genetically determined abnormal response to normal doses of a drug.
Inherited traits cause abnormal metabolism of drugs. |
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Definition
Abnormalities in the embryo resulting in a deformed fetus. |
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Pregnancy risk categories |
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Definition
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Term
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Definition
Undesirable response to a drug.
Can be common or infrequent.
Can be mild, severe or even life threatening.
Could occur after one dose or after several doses.
Some reactions are predictable, others are unpredictable. |
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Term
Allergic Drug Reactions
(Hypersensitivity Reactions) |
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Definition
Usually begin after more than one dose of the drug is given but could occur with just one dose; body views drug as antigen (foreign substance).
Could occur immediately or hours or days later.
Signs and symptoms: Itching; skin rashes; hives; wheezing; cyanosis; sudden loss of consciousness; swelling of eyes, lips or tongue. |
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Term
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Definition
Occurs shortly after administration of drug, can be fatal, treat with Epinephrine and other meds., IV fluids, antihistamines, bronchodilators. |
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Definition
Collection of fluid in subcutaneous tissues causes severe swelling of eyelids, mouth, lips, throat, can cause airway to close. |
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Definition
Unusual, abnormal reaction to drug; different from expected reaction-drug has opposite effect on the patient (sleeping pill makes patient anxious and excited), or drug causes an "over-response"-pt. sleeps for 2 days.
Cause: Believed to be due to genetic deficiency. |
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Term
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Definition
Body gets used to a drug, patient has a decreased response to the drug: Requires increased dosage for desired effect.
Example: Narcotics or tranquilizers taken for a long time. |
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Term
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Definition
Drug accumulates in body, can happen in patients with liver and kidney disease: Body unable to metabolize and excrete one dose of the drug before next dose is given.
Dose must be lowered to prevent toxic drug reaction. |
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Term
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Definition
Drug is administered in large dosages, blood concentration levels exceed therapeutic levels.
Occurs because too much of drug is given or kidneys do not excrete properly.
Sometimes can be reversed-To reverse drug toxicity: Administer another drug as antidote; monitor drugs with low safety margin. |
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