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