Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
171 Cards in this Set
- Front
- Back
a or a with accent above
|
before
|
|
ac
|
before meals
|
|
bid
|
twice a day
|
|
c with accent mark above
|
with
|
|
cap
|
capsule
|
|
d
|
day
|
|
disp
|
dispense
|
|
gm
|
gram
|
|
gr
|
grain
|
|
gtt
|
drop
|
|
h
|
hour
|
|
hs
|
at bedtime
|
|
p with accent mark above
|
after
|
|
pc
|
after meals
|
|
po
|
by mouth
|
|
prn
|
as required, if needed
|
|
q
|
every
|
|
qid
|
4 times a day
|
|
s with accent mark above
|
without
|
|
sig
|
write (label)
|
|
ss with accent marks above
|
one-half
|
|
stat
|
immediately
|
|
tab
|
tablet
|
|
tid
|
3 times a day
|
|
ud
|
as directed
|
|
the study of drugs or chemicals used for edicinal purposes
|
pharmocology
|
|
any substance other than food used in the prevention, diagnosis, alleviation, treatment or cure of a disease or for the prevention of pregnancy
|
drug
|
|
name given based upon the molecular structure if known or a code given if the chemcal structure is not known
|
chemical name
|
|
a generc name is assigned to a drug by who?
|
US Adopted Name Council
ex. aspirin |
|
trade name adopted by the manufacturer
|
brand name
|
|
prn
|
as required, if needed
|
|
q
|
every
|
|
qid
|
4 times a day
|
|
s with accent mark above
|
without
|
|
sig
|
write (label)
|
|
ss with accent marks above
|
one-half
|
|
stat
|
immediately
|
|
tab
|
tablet
|
|
tid
|
3 times a day
|
|
ud
|
as directed
|
|
the study of drugs or chemicals used for medicinal purposes
|
pharmocology
|
|
any substance other than food used in the prevention, diagnosis, alleviation, treatment or cure of a disease or for the prevention of pregnancy
|
drug
|
|
name given based upon the molecular structure if known or a code given if the chemcal structure is not known
|
chemical name
|
|
a generc name is assigned to a drug by who?
|
US Adopted Name Council
ex. aspirin |
|
trade name adopted by the manufacturer
|
brand name
|
|
Reference Bible
|
PDR
|
|
Reference manuals include
|
Mosbys, Saunders, PDR, Delmar and the electronic Epocrates.com
|
|
a drug substitution where 2 different drugs meet the same chemical AND physical ex. aspirin and acetominophen
|
chemically equivalent
|
|
a drug substitution where the same concentration of therapuedic agent is produced in the blood and tissues
|
biologically equivalent
|
|
a drug substitution where 2 different formulas have the same therapeudic effect in clinical trials
|
therapuedically equivalent
|
|
this agency
- determines physical and chemical standards of a drug - quality control manufacturing plants - determines if a drug is safe and effective |
FDA
|
|
this regulatory agency
- regulates trade practices - prohibits false advertising |
FTC
|
|
this regulatory agency
- regulates controlled substances - in under the US Dept of Justice |
DEA
|
|
a drug classified based on its mode of action/how does it work. their end result is the same
|
Biochemical reaction
|
|
drugs classified based on what they do within the body
|
physiologic effects
|
|
drugs classified based upon which organ system it targets
|
organ system
|
|
the drug and dose used as a standard of measure for pain. every drug is compared to this standard
|
10 mg of morphine
|
|
the AMOUNT of a drug required to produce a desired effect.
10 mg morphine = 60 mg codine |
potency
|
|
True or false: efficacy and potency are related
|
false. more drugs doesn't increase the intensity of the response-leads to adverse effects
|
|
the maximum EFFECT of a drug regardless of the dose
|
efficacy
|
|
at least 50% of the people will die if given x amount of dose
|
LD 50
LD50 |
|
1. a drug that likes a particular receptor
2. binds the receptor 3. produces an effect |
Agonist
|
|
counteracts the effect of the agonist
|
Antagonist (3 types)
|
|
competes for the SAME receptor site as the agonist, if successful it REDUCES the agonists effect
|
competitive antagonist
|
|
this antagonist can be reversed by increasing the concentration of the agonist. this antagonist by itself itself has no effect
|
competitive antagonist
|
|
this antagonist binds to a DIFFERENT receptor site but still reduces the effect of the agonist
|
noncompetitive antagonist
|
|
This antagonist reduces the maximum response of the agonist
|
noncompetitive antagonist
|
|
these 2 types of antagonist work on the same systems
|
competitive and non competitive
|
|
this antagonist has no effect on the agonist. it binds to a DIFFERENT receptor site but produces a effect OPPOSITE the agonist
|
physiologic antagonist
|
|
the time it takes for the drug to take effect
|
onset
|
|
the length of time the effect lasts
|
duration
|
|
a reaction not beneficial to the patient
|
adverse reaction
|
|
effect of the medication that may not be beneficial to the patient
|
side effect
|
|
if a patient is taking a drug how would you list it on the signficant findings chart?
|
name of drug, what its taken for in (), then list any adverse reactions
|
|
all drugs are measured and dispensed in what?
|
milligrams
|
|
1 kilo = __ pounds?
|
2.2
|
|
how many cc's in one ounce ?
|
30
|
|
how many teaspoons in one ounce?
|
6; 5cc's per teasp. / 30 cc's
|
|
how many cc's per teaspoon?
|
5 cc's
|
|
how many milligrams per gram?
|
1000
|
|
how many cc's per tablespoon?
|
15; 5cc's per teasp. 3 teasp. = 1 tablespoon
|
|
how many grains per milligram?
|
65 mg
|
|
1 cc is equivalent to 1 what?
|
milligram
|
|
a drug placed directly into the G.I tract ex. injested, sepository
|
enteral
|
|
drugs introduced by other means than the G.I tract ex. injection, topical, inhilation, transdermal
|
parenteral
|
|
passage from route of dministration into the circulation ex. predominately stomch to bloodstream
|
adsorption
|
|
pasage of drugs into various body fluid compartments like plasma, interstitial fluid, intracellular fluid
|
distribution
|
|
time it takes a drug to fall 1/2 of its blood level concentration. determines the duration of action
|
half-life
|
|
changing of a drug to allow for excretion. (biotransformation) active to inactive or inactive to active
|
metabolism
|
|
drugs can excrete in:
|
kidneys, saliva, lungs, sweat, GI
|
|
true or false: certain drugs will not cross the blood-brain barrier
|
true
|
|
desired effect of a drug
|
therapeutic effect
|
|
undesired effect of a drug
|
adverse effect
|
|
adverse effect caused by too high a dose or decreased metabolism
|
toxic reaction
|
|
adverse effect other than the desired therapeutic effect, dose related. ex. gastric upset with aspirin
|
side effect
|
|
adverse effect unique to one individual race or certain population
|
idiosyncratic reaction
|
|
adverse effect immune system mediated reaction, not dose related
|
allergic reaction
|
|
a drug or food potentiates (increases) or diminishes the action of another drug
|
drug interaction
|
|
an adverse effect of a drug causing birth defects
|
teratogenic effect
|
|
in order to be a true reaction, it has to be mediated by the __ system
|
immune
|
|
in this hypersensitivity reaction T-cells stimulated by a relatively harmless antigen attatch to a tissue cell
|
Type IV
|
|
in this hypersensitiity reaction an immediate, serious reaction in a previously sensitized patient. IgE mediated
|
Type I
|
|
hypersensitivity reaction where ab combines with ag and attatch to the surface of tissue cells. the immune system destroys the tissue
|
Type II
|
|
in this hypersensitivity reaction ab-ag trapped in blood vessel walls activates and stimulates inflamation leading to tissue destruction
|
Type III
|
|
the safetyness of a drug is determined by this. a ratio of LD50:ED50 the greater the # the safer its expected to be
|
therapeutic index
|
|
drugs thought to be therapeudically beneficial require a TI of __ or greater
|
10
|
|
this part of a prescription includes the personal info, Dr. phone #, and DOB and date of prescription
|
heading
|
|
this part of a prescription includes the prescription name ane dosage strength and form of drug
|
body
|
|
this part of a prescription includes the dr's sig, # of refills and DEA # if its a controlled substance
|
closing
|
|
what are the 3 requirements before a dentist can prescribe medication
|
1. they must be licensed by state board
2. u must be a patient of record 3. legitamate dental reason for prescribing |
|
schedule of controlled substance that has no therapeudic value, has the potential for abuse ex. marajuana, heroine
|
schedule 1
|
|
schedule of controlled substance with a high potntial for abuse, requires written, signed Rx NO REFILLS
|
Schedule II
|
|
Scheule of controlled substance with less abuse potential ex. valium
|
schedule IV
|
|
true or false: research institutions can obtain schedule 1 drugs
|
true
|
|
schedule of controlled substance with the least potential for abuse.
|
schedule V
|
|
a physical or mental sensation of distress or suffering usually due to an underlying etiology physical or emotional damage
|
pain
|
|
the 2 components of pain are
|
1. perception of pain
2. reaction to pain (levels of threshold) |
|
a pain reducing drug is called an
|
analgesic
|
|
2 types of analgesics are
|
1. nonnarcotic/nonopiod = PNS
2. narcotic/opiod = CNS |
|
a compound found in the bloodstream, when activated = a component of pain
|
prostaglandins
|
|
true or false: analgesics relieve the source of the pain
|
false; reduce the pain being PRODUCED not the source of the pain
|
|
true or false: non-narcotics inhibit the the making (synthess) of prostaglandins
|
true; remember reduces pain being PRODUCED
|
|
narcotics depress the CNS or PNS nd its perception of pain
|
CNS
|
|
prostaglandins irritate the nerve endings at the site of tissue damage true or false?
|
true
|
|
true or false: narcotics reduce pain reduction and block signals so pain not percieved in the brain (CNS)
|
false; narcotics DO NOT stop pain production but they DO block signals from reaching the brain (CNS)
|
|
non narcotics divided into 2 groups
|
1. salicylates (aspirin based)
2. NSAID's |
|
tissue damage causes the release of what 4 things?
|
1. histamine
2. bradykinin 3. prostaglandins 4. seratonin |
|
tissue injury results in what 4 things?
|
1. vasodilation
2. pain 3. chemotaxis (attraction of neutrophils to the site) 4. edema |
|
true or false: aspirin is a natural product of willow tree bark
|
true
|
|
the peak effect of aspirin occurs after hoe long on an empty stomach?
|
30 minutes
|
|
how does aspirin reduce fever?
|
reduces leukocyte pyrogens
|
|
aspirin is an:
___= reduces pain ___ = reduces body temp ___ = reduces inflammation ___ = reduces platelets |
analgesic
antipyretic anti-inflammatory anti-platelet |
|
true or false: generic name always in lower case unless at the beginning of a sentence, brand name is always capital
|
True
|
|
how does aspirin decrease swelling and inflammation?
|
ASA inhibits prostaglandin synthesis = decreased vasodialation and reducing inflammatory edema
|
|
how does aspirin slow the clotting mechanism?
|
inhibits prostayclin and thromboxane a and is DOSE dependant
|
|
true or false: every drug will have adverse effects to the stomach
|
true
|
|
why does asprin cause gastric irritation?
|
prostaglandin inhibtion; prostaglandin reduces gastric acid seretion and stimulates protective mucous secretion
> ACID = < MUCUS = IRRITAION |
|
name adverse effects of aspirin?
|
1. gastric > acid = irritation
2. large doses triggers chemorecptor in CNS 3. blood too thin to clot 4. Reyes syndrome = brain sweeling, kids/infants prone 5. stillbirths, hemmorage 6. hypersensitivity-allergic reaction 5-15% |
|
what is the LD50 for aspirin?
|
adults 10-30 gm
children 4 gm |
|
what are some of toxic symptoms of aspirin?
|
tinnitus: ear rining
headache nausea vomitting-chemoreceptors loss of vision |
|
what is the drug interaction of asprin with warfarin?
|
competes with aspirin for plasma proteins in the bloodstream. too much warfarin in the blood..too much bleeding
|
|
what is the drug interaction of aspirin with probeneid?
|
low doses inhibits excretion of uric acid = gout
high doses = too much uric acid |
|
what is the drug reaction of aspirin and blood pressure reducing medications?
|
may counteract blood pressure reducing medications
|
|
what does the enteric coating on aspiring do?
|
dissolves in the sall intestine vs the stomach
|
|
what is the normal dose of aspirin for adults/kids
|
adults 650 mg q 4 h
kids 60-80 mg per kg or 5mg pr lb |
|
name some combinations used with aspirin
|
1. w/another analgesic
2. w/ sedative 3. w/ buffering agents 4. w/ caffeine |
|
what is the peak for NSAID's on an empty stomach
|
1-2 hours
|
|
how do NSAID's work (similar to aspirin)
|
inhibit prostaglandin synthesis
used for mild to moderate dental pain |
|
name some adverse reactions to NSAID's
|
1. inhibits thromboxne production = prolonged bleeding while drug in system
1 day = ibuprofen, 4 days naproxen, 1 wk oxzyprozin 2. kidney failure 3. oral ulcers and xerastomia 4. longer labor-pregnancy 5. secreted in breast milk except IBUPROFEN |
|
what drugs do NSAID's interact with
|
1. lithium = bipolar disease
2. digoxin = used for CHF 3. cyclosporin = cause not to bind to plasma 4. antagonizes beta blockers, ACE inhibtors and diuretics |
|
Brand names and dose for Ibuprofen
|
Motrin,Advil more effective than ASA or ASA w/60 mg codine
|
|
Brand names and dose for Naproxen
|
Naprosyn, Alleve
|
|
Brand name and dose for Acetaminphen
|
equal to ASA without the platelet effect, no gastric bleeding and no effect on reducing inflammation
|
|
true or false; opioids are controlled substances
|
true
|
|
true or false; opioids work at the PNS by raisn the pain thresholds
|
false; CNS
|
|
how are opiods absorbed?
|
orally, transmuscosally, trandermally cn be injected by not reccommended; onset within an hour
|
|
what is the distribution of opioids?
|
bound to plasma proteins on a "first pass"
|
|
what is the metabolism of opioids?
|
conjugates with gluuronic acid in the liver; duration 4-6 hours
|
|
the strongest opioid and standard of measure
weakest? |
morphine
codiene |
|
side effects of opioids?
|
1. sedation/euphoria
2. cough suppression 3. gastrointestinal muscle relaxtion |
|
adverse reactions of opioids?
|
1. respiratory depression
2. nausea/emesis (vommitting) 3. constipation 4. myosis (dialated pupils) 5. urinary retention 6. stimulates histamine release 7. crosses placental barrier depresses fetal respiration |
|
true or false; nausea is an allergic reaction
|
false
|
|
This brand name of Hydrocodone relieves moderate pain alone or with ASA or acetominophine
|
Lortab or Lorcet
|
|
opiod that relieves moderate to severe pain alone or in combo with ASA or acetominophine
|
Oxycodone
|
|
most common opioid; questionalble efficacy usually used in combo with ASA or acetominophines
|
Codeine
|
|
This brand name of Propoxyphene has a questionable efficacy and is usually used in combo with ASA or acetominophine
|
Darvon Darvocet
|
|
Commonly abused opioid by health professional 100mg = 10 g morphine
|
Meperidine
|
|
Opioid not used in dentistry; has a high abuse potential outlawed in mahy states
|
Hydromorphone
|
|
used for withdrawl of morphine
|
methadone
|
|
This brand of Naloxne competes with opioids for receptor sites; used for overdose reversal
|
Narcan
|
|
used in opioid free addicts to maintain opioid free state
|
Naltrexone
|