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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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