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128 Cards in this Set

  • Front
  • Back
broad description of a drug or medication; includes mechanism of action, pharmacokinetic/dynamic parameters, drug interactions, adverse effects, toxic effects
Pharmacology
pharmacology + disease state + patient; takes into consideration the pharmacology of a medication and broadens the concept by looking at how to use the medication in patients with various disease states
Pharmacotherapeutics
basically, too many medications are taken by a patient; very common in the elderly; very common in patients seeing multiple practitioners
Polypharmacy
what the body does to the drug; absorption, distribution, metabolism, elimination
Pharmacokinetics
what the drug does to the body; mechanism of action
Pharmacodynamics
considers genetic factors (in patients) that may have an effect on a drug’s responsiveness
Pharmacogenetics
aka “drug targets); specific target where a medication will “do its job” or exert its effect; receptors may be a membrane protein, an enzyme, or a nucleic acid; the “lock and key hypothesis”— the drug and receptor must be structurally complementary to recognize each other and exert an effect
Receptor
meds that bind to a receptor and activate it
Agonists
meds that bind to a receptor, but that do not have the exact structural features needed to activate it
Antagonists
drug administration -> PO (oral)
Enteral administration
drug administration -> IV (intravenous), IM (intramuscular), SC (subcutaneous)
Parenteral administration
place medication on the skin or mucous membranes for absorption
Topical
circulation; vascular space; where most medications go once they are absorbed PO; where IV medications go immediately
Systemic
An order for medication issued by a physician or properly licensed medical practitioner.
Prescription
medications, which may be dispensed legally when issued by a physician or properly, licensed medical practitioner. Also termed “Legend drug”.
Prescription Drugs
medication purchased without a prescription also termed over-the-counter (OTC) drug.
Nonprescription Drug
printed forms that contain blanks spaces for required prescription information.
Prescription Blank
are drugs which because of the potential for abuse, are controlled under special regulations by the federal government.
Controlled Substances
prescription orders requiring the pharmacist to mix ingredients.
Compounded Prescription
abv -> ac
before meals
abv -> ad
right ear
abv -> as
left ear
abv -> am
before noon, morning
abv -> Amp
Ampule
abv -> aq
water
abv -> ATC
around the clock
abv -> au
each ear
abv -> bid
twice a day
abv -> bm
bowel movement
abv -> BSA
Body surface area
abv -> C
with
abv -> Caps
Capsules
abv -> cc
cubic centimeter (equivalent to milliliter)
abv -> Dil
dilute
abv -> DC, disc
an order to stop medication, discharge
abv -> DW
distilled water
abv -> D5W
dextrose 5% in water
abv -> g, gm or Gm
gram
abv -> gr
Grain
abv -> gtt
a drop
abv -> h or hr
hour
abv -> ha or h/a
headache
abv -> hs or HS
at bedtime
abv -> ID
intradermal
abv -> IM
intramuscular
abv -> Inj
injection
abv -> IV, iv
intravenous
abv -> IVP
intravenous push
abv -> Liq
solution
abv -> mcg or ug
microgram
abv -> MEq
Milliequivalent
abv -> mg
milligram
abv -> mg/kg
mg of drug per kilogram of body weight
abv -> mg/m2
mg of drug per sq. meter of body surface area
abv -> ml or mL
milliliter
abv -> NPO
nothing by mouth
abv -> NS or NSS
normal saline or normal saline solution
abv -> N & V
nausea & vomiting
abv -> od
right eye
abv -> os
left eye
abv -> ou
each eye
abv -> pc
after meals
abv -> pm
afternoon, evening
abv -> po
by mouth
abv -> prn
as/when necessary or when required
abv -> Q or q
each, every
abv -> Qd or qd
every day
abv -> Qh or qh
every hour
abv -> qid
four times a day
abv -> qod
every other day
abv -> qs
as much as sufficient
abv -> rect or R
use rectally
abv -> repet
let it be repeated
abv -> s
without
abv -> Sig
(you) write
abv -> sl
subligual (under the tongue)
abv -> ss
one-half
abv -> Stat
immediately
abv -> subc or subq or sc or sq
subcutaneously
abv -> supp
suppository
abv -> susp
suspension
abv -> Syr
syrup
abv -> tab
tablet
abv -> Tbsp
tablespoon
abv -> tid
three times a day
abv -> tiw
three times a week
abv -> tsp
teaspoon
abv -> U or u
unit
abv -> ud
as directed
abv -> ut dict
as directed
abv -> L
Fifty
abv -> C
one hundred
abv -> D
five hundred
abv -> M
one thousand
100 mg or 100mg?
100 mg
1 mg or 1.0 mg?
1 mg
.1 mL or 0.1 mL?
0.1 mL
unit or U?
unit
mg. , Mg. , mg , Mg , MG , mgm , mgs?
mg
mL., ml., mls, mLs, mL, cc, ml?
mL or ml
When drug molecules are released from dosage form
dissolution
When drug molecules are absorbed across biological membranes to reach systemic circulation
absorption
The fraction of drug absorbed into the systemic circulation after extravascular administration.
bioavailability
PO-> to gut -> to liver via portal circulation
1st pass effect
List drug factors that affect absorption
lipophilicity, hydrophilicity, ionization state, molecular weight
Point where the amount of drug delivered to the body = the amount of drug being eliminated from the body in one t 1/2
steady state concentration
How many serum half lives does it take to reach steady state concentration?
5
The way in which drugs are administered in order to maintain a steady state of drug in the body
Maintenance Dose
A dose that raises the concentration of drug in plasma to the target concentration; this may be desirable when the time to reach steady state (Css) is long
Loading Dose
The highest point (concentration) in the blood stream after administration of the drug
Peak drug concentration
The lowest point (concentration) in the blood stream – usually immediately before next dosing interval
Trough drug concentration
Range of concentrations within which the pharmacologic response is produced and the adverse effects are prevented
Therapeutic Range
relates the amount of drug in the body to the serum concentration; reflects the extent to which a drug is present in extravascular tissue
Volume of distribution
Single most important factor in determining drug concentrations; determines the steady-state concentration (Css) for a given dosage rate
Clearance
Identify the 3 factors involved in the calculation of drug clearance
dose, organ blood flow, function of liver or kidneys
Serum creatinine has an inverse relationship with ________ function.
kidney
Any ______ ________ medication should be dose-adjusted <= 60 ml/min
estClCr.
renally cleared
____________ and ______________ transform meds into more polar compounds which allows them to be excreted
Metabolism, biotransformation
Usually occur somewhere between absorption of med into systemic circulation and the med’s renal elimination
Biotransformations
T or F -> The kidneys are the primary organs of drug metabolism.
F The liver is the primary organ of drug metabolism.
Usually convert the parent drug into a more polar metabolite (may be an active metabolite or an inactive metabolite); modify structure
Phase I reactions
Combines ("conjugates") drug with large, H2O soluble polar molecules to increase solubility and excretion into the urine.
Phase II reactions
Dose-response relation of one drug is altered by another drug
Drug-drug interaction
enhances therapeutic efficacy
Synergism
reduces therapeutic efficacy
Antagonism
Can be considered as "positive" drug interactions
Additive Effect
Are negative drug interactions which have the possibility of going unnoticed for some time
Diminished Effect
These interactions, which are considered negative, cause the medications to have an unexpected outcome.
Altered Effect