test 1 Flashcards
supp
Suppository
gtt
drops
AM
before noon
cap
capsule
hs
at bedtime (hour of sleep)
OD
right eye (oeil droit)
PM
afternoon
tid
three times daily
qod
every other day
q
every
q2h
every 2 hours
ss
half
d/c
discontinue
stat
immediately
Ac
before meals
bid
twice daily
g, gm
gram
IM
intermuscular
OS
left eye
PO
by mouth
Qid
four times a day
qd
every day
SC,SQ
subcutaneous
tsp
teaspoon
susp
suspended
tinct
tincture
Aq
aqueous
IU
international units
ad lib
as desired
AAT
activity as tolerated
IVPB
iv piggyback
c
with
h, hr
hour
IV
intravenous
pc
after meals (post cibum)
prn
as needed (pro re nata)
qh
every hour
qs
as much as suffices
SL
sublingual
tbsp
tablespoon
NS
normal saline
cf
with food
The name that describes the chemical composition and molecular structure of a drug.
chemical name
The name given to a drug approved by Health Canada; also called the nonproprietary name or the official name (EG. ACETAMINPHEN)
generic name
indicates that the drug has a registered trademark and that its commercial use is restricted to the owner of the patent for the drug until the patent expires. (EG. TYLENOL)
trade name
a drug that is sold without a prescription
Over the counter drugs (OTC)
The letter N is printed on the label of all _____________ agents
narcotic
The rate of drug distribution among body compartments after a drug has entered the body, includes 4 stages
Pharmacokinetics
The study of the biochemical and physiological interactions of drugs at their sites of activity.
Pharmacodynamics
interaction where a drug binds to proteins in the body
Protein binding
soluable in lipids
Lipid solubility
the series of chemical alterations of a compound (e.g., a drug) occurring within the body, as by enzymatic activity
Biotransformation
A molecular structure within or on the outer surface of cells to which specific substances (e.g., drug molecules) bind.
Receptors
the time required after administration of a drug for a response to be observed; the length of time needed for a medicine to become effective
Onset of action
The time period when the effect of something is at optimal strength
Peak of action
The length of time that a particular drug is effective
Duration of action
A drug that binds to and stimulates the activity of one or more biochemical receptor types in the body
Agonists
A drug that binds to and inhibits the activity of one or more biochemical receptor types in the body, resulting in inhibitory drug effects; also called inhibitors
Antagonists
The ratio between the toxic dose and the therapeutic dose of a drug, used as a measure of the relative safety of the drug for a particular treatment
Therapeutic Index
The maximum concentration of a drug in the body after administration, usually measured in a blood sample for therapeutic drug monitoring
Peak drug level
The lowest concentration of a drug reached in the body after it falls from the peak level, usually measured in a blood sample for therapeutic drug monitoring.
Trough level
The condition of producing adverse bodily effects because of poisonous qualities
Toxicity
a large initial dose of a substance or series of such doses given to rapidly achieve a therapeutic concentration in the body
Loading dose
a symptom or particular circumstance that indicates the advisability or necessity of a specific medical treatment or procedure
Indications
Any condition, especially one related to a disease state or other patient characteristic, including current or recent drug therapy, that renders a particular form of treatment improper or undesirable
Contraindications
the means by which a drug exerts a desired effect. Drugs are usually classified by their actions; for example, a vasodilator, prescribed to decrease the blood pressure, acts by dilating the blood vessels
Desired action
A peripheral or secondary effect, especially an undesirable secondary effect of a drug or therapy
Side effects
Any undesirable bodily effects that are a direct response to one or more drugs
Adverse effects
An immunological hypersensitivity reaction resulting from the unusual sensitivity of a patient to a particular medication; a type of ADE.
Allergic reactions
The fraction of drug in serum that is not bound to a carrier protein or other molecule, which generally is pharmacologically active
Unbound drugs
In pharmacokinetics, the time required for one half of an administered dose of drug to be eliminated by the body
Half life
Drug interactions in which the effect of a combination of two or more drugs with similar actions is equivalent to the sum of the individual effects of the same drugs given alone
Additive effect
Alteration of the pharmacological activity of a given drug caused by the presence of one or more additional drugs
Drug interactions
the effect produced when some drugs and certain foods or beverages are taken at the same time. For example, grapefruit juice blocks the metabolism of some drugs in the GI tract, an action that can cause normal dosages of a drug to reach toxic levels in the plasma
Food drug interactions
refers to anything involving the alimentary tract, from the mouth to the rectum.
Enteral route
4 enteral routes of administration:
oral,
sublinqual,
buccal,
rectal.
- Located outside the alimentary canal; 2. Taken into the body or administered in a manner other than through the digestive tract, as by intravenous or intramuscular injection.
Parenteral route
a path of entry via the skin
Percutaneous route
Any chemical that affects the physiological processes of a living organism
Drug
Broadest term for the study or science of drugs.
Pharmacology
The science of preparing and dispensing drugs, including dosage form design (e.g., tablets, capsules, injections, patches, etc.).
Pharmaceutics
Pharmacokinetics is the study of what the body does to the drug including the following 4 processes:
Absorption
Distribution
Metabolism
Excretion
A measure of the extent of drug absorption for a given drug and route (can vary from 0% to 100%).
bioavailability
Drug interactions in which the effect of a combination of two or more drugs with similar actions is greater than the sum of the individual effects of the same drugs given alone
Synergistic effects
The initial metabolism in the liver of a drug absorbed from the gastrointestinal tract before the drug reaches the systemic circulation through the bloodstream.
first-pass effect
An abnormal and unexpected response to a drug, other than an allergic reaction, that is peculiar to an individual patient
Idiosyncratic reaction
The time required for a drug to elicit a therapeutic response after dosing.
onset of action
The chemical form of a drug that is administered before it is metabolized by the body’s biochemical reactions into its active or inactive metabolites
parent drug
Pain that is sudden in onset, usually subsides when treated, and typically occurs over less than a 6-week period
acute pain
Strong psychological or physical dependence on a drug or other psychoactive substance, usually resulting from habitual use, that is beyond normal voluntary control
addiction
A substance that binds to a receptor and causes a partial response that is not as strong as that caused by an agonist (also known as a partial agonist).
Agonist–antagonist
A phenomenon that occurs when a given pain drug no longer effectively controls a patient’s pain despite the administration of the highest safe dosages.
analgesic ceiling effect
Medications that relieve pain without causing loss of consciousness (sometimes referred to as painkillers).
analgesics
Pain that lingers despite doses of a long-acting dosage form for every 12 hours.
breakthrough pain
A common and well-described theory of pain transmission and pain relief. It uses a gate model to explain how impulses from damaged tissues are sensed in the brain
gate theory
Pain that results from a disturbance of function or pathological change in a nerve
neuropathic pain
Pain that arises from mechanical, chemical, or thermal irritation of peripheral sensory nerves (e.g., after surgery or trauma or associated with degenerative processes)
nociceptive pain
A large, chemically diverse group of drugs that are analgesics and possess anti-inflammatory and antipyretic activity but are not steroids.
Nonsteroidal anti-inflammatory drugs (NSAIDs)
A natural narcotic drug containing or derived from opium that binds to opiate receptors in the brain to relieve pain
opiate analgesic
A synthetic narcotic drug that binds to opiate receptors in the brain to relieve pain
Opioid analgesic
Describes patients who are receiving opioid analgesics for the first time and who therefore are not accustomed to their effects
opioid naive
A normal physiological condition that results from long-term opioid use, in which larger doses of opioids are required to maintain the same level of analgesia and in which abrupt discontinuation of the drug results in withdrawal symptoms (same as physical dependence)
opioid tolerance
The signs and symptoms associated with abstinence from or withdrawal of an opioid analgesic when the body has become physically dependent on the substance.
opioid withdrawal