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149 Cards in this Set
- Front
- Back
Def- Study of effects of chemical substances on living tissue
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Pharmacology
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Def- The application of pharmacology to prevent or treat disease- 2 terms
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Pharmacotheraputics or clinical pharmacology
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What year was the Drug Regulation Reform Act passed?
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1906
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Def- Regulates perscription drugs in the US
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Federal Food and Drug Administration (FDA)
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This act was passed to protect the public by controlling the sales of drugs which were altered, dangerous, and falsely labeled.
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The Federal Food and Drug Act of 1906
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This was designed in 1906 as the official listings of all drugs legally available in the US
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US Pharmacopeia
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This was designed in 1906 as the official listing of all drugs available in the US
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The National Formulary
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Which amendment was passed to prohibit drug companies from making false claims about their products? What year was it passed?
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FDA-Sherley Amendment passed in 1912
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What act defined the legal term "Narcotic" and regulated the important, manufacturing and sale of opium, cocaine, and their derivatives? What year was this first narcotic act passed?
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The Harrison Narcotic Act passed in 1914
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What law enabled pharmaceutical companies to manufacture and market a drug under the generic name and to apply their own trade name once the patent held by the original manufacture expired. What year was this law passed?
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Generic Drug Law passed in 1984
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How many years and how much does it cost to bring a new drug to the market?
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14 years and can cost up to 980 million dollars
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How long is a patent usually granted for?
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13-17 years from the time the drug is invented.
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During this stage in the drug trial drugs are administered to animals
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Pre-clinical trials
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How many stages does the clinical trial on humans progress through?
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Four
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In this Phase the drug is given to a small number of healthy volunteers to determine the biological effects of the drug in humans and dosage ranges. This usually takes place in out-patient clinical research centers.
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Phase I
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In this stage the drug is only given to a small number of volunteers who have the disorder the drug is intended to treat
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Phase II
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In this phase the drug is perscribed to a large number of patients who have the disorder the drug is intended to treat. In this stage the drug may be compared with a placebo or with an established drug.
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Phase III
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After what stage can the pharmaceutical company submit a "new drug application"
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Phase III
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This phase is refered to as the post-marketing surveillance. During this phase adverse side effects may be encountered resulting in drug being pulled from the market. FDA and pharmecutical company revceive feedback from HCP.
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Phase IV
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What are the three main factors that clinical trials are currently surrounded by ethical issues?
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1) fewer people in america are volunteering for clinical trials
2) the pharmaceutical companies incur large research and development costs during all phases of the clinical trials 3) The FDA imposes rigid regulations on drug testing on humans. |
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What three names are drugs given?
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1) chemical
2) generic 3) trade. brand or proprietary |
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Which name can vary from company to company?
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brand name
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Def- Taking many drugs that interact with each other, one drug causes a reaction and another drug is given to treat
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Polypharmacy
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What are the FIVE "R"'s?
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Right Patient, Right Drug, Right Time, Right Route, Right Dose
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TRUE OR FALSE
Agency policies cannot be broader than the state nurse practice act. |
TRUE
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TRUE OR FALSE
The nurse is legally responsible for knowing the purpose, therapeutic effects and possible adverse effects of drugs administered. |
TRUE
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Is q.d. or Q.D. on the Do Not Use List?
If so what should be used? |
example of DO NOT USE;
"daily" or "every day" should be used |
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Do Not USE?
q.o.d. , Q.O.D What should be used? |
DO NOT USE; "every other day" should be used
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Do NOT USE?
U |
DO NOT USE;
"unit" should be used |
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DO NOT USE?
IU |
DO NOT USE;
"INternational Unit" should be used |
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DO NOT USE?
MS, MSO4 |
DO NOT USE;
"morphine sulfate" should be used |
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DO NOT USE?
MgSO4 |
DO NOT USE;
'magnesium sulfate" should be used |
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TRUE FALSE? always add a zero before a decimal point?
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TRUE; .6 should be recorded as 0.6
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TRUE FALSE? DO NOT ADD A DECIMAL POINT OR A ZERO AFTER A WHOLE NUMBER?
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TRUE ; 1.0mg should be written 1mg
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c.c.
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preferred abbreviation "mL" milliliter
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ug
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preferred abbreviation "mcg"
microgram |
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>
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perferred write out 'greater than"
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<
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preferred write out "less than"
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TRUE FALSE? Drug abbreviations can be used?
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FALSE Write the whole word out
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Apothecary units should be replaced with what?
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metric units instead
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@
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write "at"
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cap
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Capsule
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dr
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dram
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elix
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elixir
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g,gm, G, GM
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gram
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gr
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grain
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gtt
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drops
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kg
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kilograms
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l,L
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liter
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m2
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square meter
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mcg, ug
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microgram
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mEq
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milliequivalent
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mg
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milligram
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mL, ml
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milliliter
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m, min
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minim
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oz
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ounce
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pt
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pint
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qt
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quart
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SR
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sustained release
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__
ss., ss |
one half
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supp
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suppository
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susp
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suspension
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T.O.
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telephone order
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T, tbsp
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tablespoon
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t, tsp
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teaspoon
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V.O.
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verbal order
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A.D. ad
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right ear
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A.S. as
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left ear
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A.U. au
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both ears
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ID
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intradermal
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IM
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intramuscular
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IV
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intravenous
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IVPB
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intravenous piggyback
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KVO
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keep vein open
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L
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left
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NGT
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nasogastric tube
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O.D. od
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right eye
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O.S. os
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left eye
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O.U. ou
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both eyes
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PO po os
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by mouth
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SC subc sc SQ subQ
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subcutaneous
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SL sl subl
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sublingual
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TKO
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to keep open
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Vag
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vaginal
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AC ac
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before meals
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ad lib
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as desired
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B.i.d b.i.d
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twice a day
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_
c |
with
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Hs
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hour of sleep
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NPO
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nothing by mouth
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PC pc
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after meals
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PRN p.r.n.
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whenever necessary, as needed
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Q
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every
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Oam
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every morning
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Qh
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every hour
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q2h
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every 2 hours
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q4h
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every 4 hours
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q6h
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every 6 hours
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q8h
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every 8 hours
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s |
without
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SOS
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once if necessary: if there is a need
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Stat
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immediately
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T.i.d t.i.d.
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three times a day
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adverse to fetus
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teratogenic
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No risk to fetus. Studies have not shown evidence of fetal harm
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A
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no risk in animal studies, and well controlled studies in pregnant women are not available. It is assumed there is little to no risk in pregnant women.
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B
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Animal studies indicate a risk to fetus. Controlled studies on pregnant women are not available. Risk versus benefit of the drug must be determined.
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C
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A risk to the human fetus has been proved. Risk versus benefit of the drug must be determined. It could be used in life-threatening conditions.
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D
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A risk to human fetus has been proved. Risk outweighs the benefit, and drug should be avoided during pregnancy.
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X
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PEG
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percutaneous endoscopic gastic tube
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PR
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rectal
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IVP
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intravenous push
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hs
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hour of sleep, bedtime
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cc
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cubic centimeter
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ss
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1/2
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I
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one
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V
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five
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X
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ten
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1 gram = _______ mg
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1000mg
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1mg=________mcg (ug)
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1000 mcg (ug)
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1 liter= _____mL
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1000mL
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1 meter (m) = _____ millimeters (mm) & = _______ centimeters (cm)
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1000 mm
100 cm |
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1 cm= ___ mm
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10 mm
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1 grain (gr) = ___ or____ mg
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60 or 65
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15 or 16 grains (gr) = ____ grams (g, gm)
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1 gram
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16 ounces (oz) = ____ pounds (Ib)
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1 pound (lb)
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2.2 pounds = ___ kg
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1 kg
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1 inch = ___ cm
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2.54cm
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1 mL= ___to___ minims (m)
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15-16 minims
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1 dram (dr) = ___ mL
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4 mL
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1 ounce (oz) = ____ mL
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30 mL
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1 pint (pt)= ___mL
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500mL
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2 pints = ___ quart (qt)
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1 quart
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1 qt = ___ liters
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1 liter
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4 qt = ___ gallons
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1 gallon
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1 teaspoon =__ mL
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5 mL
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3 teaspoons =___ tbsp
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1 tbsp
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1 cup= ___oz
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8 oz
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8 oz = ____ mL
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240mL
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To calculate Fahrenheit to Celsius?
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(F-32) /1.8 = C
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To calculate Celsius to Fahrenheit?
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[ 1.8 (C) ] + 32 = F
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Opposite of intended effects
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Paradoxic
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pt knows options, benefits, cost, and signs consents, knows why med is being given verbal and written
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informed consent
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pt has the right to refuse medication, right to self determination.
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Autonimy
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an unintended unknown effect is presented after administration of a drug
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idiosencratic
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intended effect is presented after administration of a drug
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theraputic
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unintended but known side effect is presented after administration of a drug
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side effect
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problems occur which are major
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adverse effect
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too much drug administered in system severe adverse effect
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toxic
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