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study guide

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Term
Definition
pharmacodynamics   ways in which drugs work to change body function; the study of how drugs work with other medications, enzymes or cell receptor sites in the body  
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pharmacokinetics   the study of how drugs move through the body; mechanism of action drug metabolism  
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four steps of pharmacokinetics   1. absorption - how it gets into bloodstream 2. distribution - how it gets to target tissue 3. metabolism - how cells convert drug for use 4. elimination - how it is removed from body  
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pharmaceutics   ceutic = magician + pharmakon = drug the science of preparing and dispensing drugs to a patient after he or she has been examined by a licensed HCP  
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factors affecting absorption   where and how much was given  
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intrinsic drugs   chemicals that the body makes; hormones, enzymes, growth factors etc  
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extrinsic drugs   made outside the body, must be taken into the body to change cell, organ or body action  
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OTC - what must the patient know   have less potential for harmful side effects, no prescription required, allow you to control your own health care, can still cause health problems and may interact with prescription drugs  
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generic name   always lower case, USAN creates generic names, some part of all generic names for drugs of one class will be the same (-statin, -olol) once a name is approved it is public and not owned by any one drug company  
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brand name   created by each drug company, always capitalized, will have a TM (trademark) or R (registered) after the name  
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steady state   balancing drug entry with drug elimination  
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why discuss herbal supplements with pharmacist   herbal supplements have cellular effects that can be harmful or can interact with other drugs, people may take large quantities because if a little is good for me then a lot is better for me,  
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organ of elimination of drugs from the body   intestinal tract, kidneys and lungs  
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2 patient identifiers   name and birth date  
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7 Rights   1. right patient 2. right drug 3. right dose 4. right route 5. right time 6. right documentation 7. right to refuse a drug  
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SL   sublingual  
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PO   oral (per os)  
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BID   twice per day  
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TID   three times per day  
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standing order   an order written when a patient is to receive a drug on a regular basis  
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High alert drugs   P-potassium I-insulin N-narcotics C-chemotherapy agents H-heparin  
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agonist   mimics intrinsic drugs activates receptor site  
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antagonist   blocks receptor sites so intrinsic drugs can not bind, slows or stops the activity; it is similar so that it binds to receptor site but doesn't activate it; competes with intrinsic drug  
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nonreceptor actions   does not use receptors  
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physiological effect   outcome of the mechanism of action of a drug, expected and unexpected response, allergic reaction, personal (idiosyncractic)  
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side effects   mild changes  
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adverse effects   (ADR)harmful side effect more severe than expected toxic or toxicity  
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bioavailability   the amount of drug dose that acturally reaches the bloodstream  
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percutaneous   skin or mucous membrane, must be lipid soluble, a drug placed in lowest 1.5 inches of rectum  
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enteral   GI tract drug placed high in rectum, feeding tubes  
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parenteral   injection, IV drugs are 100% bioavailable  
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compartments   1st - blood stream or blood volume 2nd - blood volume and interstitial spaces 3rd - blood volume, interstitial spaces and intracellular spaces  
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hydrophilic drugs   limited on entering intracellular spaces  
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fist-pass loss   rapid inactivation or elimination of oral drugs as a result of liver metabolism  
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when is a drug considered eliminated   when less than 10% of the drug remains in the system in general it is 5 half-lives after the last dose  
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paradoxical effect   effect of a drug is opposite expected effect  
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toddler through adolescent   have higher metabolism than an adult, a drug would be given at a lower dose but more often  
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infants and young children   water soluble drugs are eliminated faster due to increased water content and surface area  
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teratogenic or teratogens   drugs that cause birth defects 3rd-8th week is most critical time of embryo development  
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category A   studies show no risk to fetus  
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category B   no studies on humans, animal studies show no risk to fetus  
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category C   no studies have been done on humans or animals  
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category D   human studies show increased risk to fetus  
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category X   studies show risk to fetus DO NOT GIVE TO PREGNANT WOMEN  
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nurses role   administer drug, teach, know desired effects and side/adverse effects  
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minimum info on written RX   date , patient name, name and address of subscriber, generic or brand name of drug, strength, times taken per day, instructions, number of doses to dispense, number of refills, prescriber's signature,  
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principle of administration of drugs   must know the drug know pt drug history, allergies, ADR, lab values and changes in condition be aware of prescribed limitations listen to the patient  
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enteral drugs   Before: check order, wash hands, check identifiers, check wrist band After: document, check pt for side effects, ADR and desired effects  
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feeding tube (enteral)   Before: check about crushing tablets or opening capsules, sit pt upright, withdraw stomach contents with syringe or use end-tidal CO2 detector to make sure tube is in stomach After: flush with 50 mL of water; if suction is used, clamp tubing for 30 mins  
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Rectal drugs   Before: does pt have diarrhea, surgery or trauma to rectum? know history of vasovagal reaction use sims position (left lateral) lubricate suppository insert about 1 inch  
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Parenteral drugs   IV IM intradermal Subcutaneous  
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interdermal drugs   3/8 inch, 25 guage between layer of skin 15 degree angle, bevel up DO NOT aspirate drug volume - 0.01 to 0.1 mL  
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subcutaneous   3/8 to 5/8 inch, 25-27 guage between skin and muscle 45 degree angle (90 degree if pt is obese) aspirate for anything except insulin or heparin apply pressure drug volume - 0.5 to 1 mL  
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IM   1-1.5 inches, 20-22 guage use deltoid, vastus lateralis or dorsogluteal muscles 90 degree angle aspirate drug volume: children no more than 1 mL, adults no more than 3 mL  
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Z track   if drug is irritating or would permantly stain tissue; pull tissue laterally and hold while injecting drug  
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IV   check patency of IV site remove air from tubing document site and flow rate check for infection, extravasation (fluid escaping from vein) and infiltration (fluid collecting in tissues)  
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Percutaneous drugs   absorption affected by size of area, concentration of drug, contact time, condition of skin  
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topical drugs   applied to skin for local effects  
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transdermal drugs   applied to skin but enters blood stream  
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topical/transdermal drugs   clean area,apply in smooth, thin layer, cover area remove old patch, clean site (previous also), rotate sites: for children, place a transdermal patch on back between shoulder blades  
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mucous membranes   includes: buccal, sublingual, eyes, ears, nose, inhaled, vagina  
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learning   to acquire new knowledge that results in a persistent change of behavior  
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listening   the key to know what is taught is actually being learned  
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cognitive   intellectual learning  
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psychomotor   motor skills  
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affective domain   attitudes, values, interests, appreciation and adjustment - helps the pt value information - motivation, longest lasting form of learning  
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androgogy   adult learning  
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pedagogy   child learning  
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give this info clearly to pt   drug name, purpose of drug, how it works, how to take it, special instructions, expected response, side effect, ADR, when to call provider  
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polypharmacy   pt is prescribed many drugs  
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normal body temp   97-100 F 36.1-37.8 C  
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Celsius to Fahrenheit   (C x 1.8) + 32 round to tenth  
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Fahrenheit to Celsius   (F - 32)/1.8 round to tenth  
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60 gtt   1 tsp  
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15 gtt   1 mL  
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3 tsp   1 TBS  
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1 tsp   5 mL  
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2 TBS   1 oz or 30 g or mL  
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8 oz   240 mL  
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16 oz (1 pt)   454 g (dry) 500 mL  
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32 oz (1 qt)   1000 mL  
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4 qt   1 gallon  
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mEq   used to measure electrolytes: KCl, KPO4, Ca++  
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Mother killed her dog under duress cause Max made noise (my favorite mnemonic)   M K H D U D C M . . M . . N  
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compared to basic unit   K 1000 H 100 D 10 d 0.1 c 0.01 m 0.001 mcg 0.000001 micro gram 0.000000001  
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drug error   most caused due to not following one or more of the rights  
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pounds to kilograms and vise versa   lb / 2.2 kg x 2.2  
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inch to centimeter   inch = 2.54 cm  
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buccal drugs   given between cheek and molar teeth of upper jaw  
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sublingual   placed under tongue  
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controlled substance   Controlled substances are drugs that have some potential for abuse or dependence. These drugs are regulated by the federal Controlled Substances Act (CSA) – this law helps the US Government fight against the abuse of these drugs.  
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half-life   time span needed for half of the drug to be eliminated.  
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peak and troughs   peak=maximum blood drug level: trough= minimal blood drug level  
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prodrug   an inactive substance that is converted to a drug within the body by the action of enzymes or other chemicals.  
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what factors slow the absorption of drugs   affected by anything occurring in the stomach or intestines. diarrhea can move the drug too quickly, calcium can bind with some drugs and keep them from absorbing,  
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what factors affect drug distribution   size and chemical nature of the drug, dehydration, low blood pressure, trapping of the drug in certain tissues (sequestration)  
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single dose order   an order to give a drug once only  
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PRN order   given to the pt as needed  
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stat order   given ASAP, per class notes you have 10 minutes to give a stat order  
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right time   you have a 30 minute window to give ordered drugs in order to stay within the "right time"  
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sentinel event   A sentinel event is an unexpected occurrence involving death or serious physical or psychological injury, or the risk thereof  
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what drug route is most dangerous   IV, 1. the IV may infiltrate. 2. it is expensive and nursing intensive. 3. rapid administration of a drug can lead to toxicity. 4. the patient always has more side effects.  
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