Module 1 and 2 Flashcards
nuovo receptario
1st official pharmacopoeia
William Proctor, Jr.
father of American pharmacy
helped to compose and produce the United States Pharmacopeia (USP) in 1820
capsules
small, oblong, gelatin containers
tablets
wide variety of shapes and sizes
may be chewable, effervescent, enteric-coated, troches, or lozenges
orally dissolving
buccal
sublingual
orally disintegrating
films
immediate release vs. controlled release
suspensions
medication is suspended in liquid
reconstituting powders to liquid
must be mixed by shaking before administration
liquid dosage forms
elixirs
fluid extractions and tinctures
spirits or essences
syrups
emulsions
topical dosage forms
ointments
creams
lotions
liniments
gels
collodions
transdermal patches
suppositories
vaginal tablets
otic and ophthalmic preparations
other dosage forms
aerosols
sprays
chewing gum
parenteral (must be sterile preparation, injection sites can be IV, IM, or SQ)
vials
plastic, often amber-colored cylinders used to dispense oral solids
ointment jar
plastic or glass containers used to dispense ointments and creams
bottles
plastic, often amber-colored bottles used to dispense oral liquids
child-resistant
must be simultaneously pushed down and twisted to open
easy open
easily opened to allow quick access to medication
medications not requiring child-resistant closures
isosorbide dinitrate sublingual and chewable (isordil)
oral contraceptives in unit-of-use packages
cholestyramine powder (questran)
potassium powders and tablets in packets (k-lyte)
methylprednisolone tablets in unit-of-use packages (medrol dosepak)
mebendazole tablets (vermox)
metered-dose inhalers Albuterol sulfate (proventil)
nitroglycerin SL tablets (nitrostat)
generic medication
official name derived from the chemical name, structure, or class of medication
ex: acetaminophen (Tylenol)
active ingredients are the same as brand name medications
lower cost
sometimes required by insurance
brand name medication
trademark name given by manufacturer
ex: tylenol
patents expire 20 years after medication was invented
patent period is used to recover research and development cost
once patent expires, generic versions can be sold
generics permitted
allows for patient to receive a generic medication if one is available
brand name only
dispense as written (DAW)
brand medically necessary or no substitution allowed
generic product evaluation
pharmaceutical equivalents, pharmaceutical alternatives, therapeutic equivalents, therapeutic alternatives, bioequivalents, and narrow therapeutic index
stock bottle label requirements
names, strength, legend statement, storage requirements, quantity, dosage form, manufacturer, controlled-substance mark, lot number, expiration date, national drug code (NDC)
NDC numbers
11-digit codes assigned by the manufacturer
identifies the manufacturer, product, and package size
easily confused products
look-alike and sound-alike (LASA) medications use tall man lettering to help prevent medication errors
public safety and reporting errors
medwatch is a voluntary reporting system for adverse effects and medication errors with pharmaceutical products
reports can be made by phone, online, mailing, email, or fax