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what unit systems are used in compounding?
apothecary and metric
when are approximate equivalents such as dram symbol used?
when translating directions into patient language
in already made (manufactured) products
NOT in compounding
define percentage error
maximum potential error x 100 / quantity desired
prescription
an order for medication issued by a physician, dentist, or other properly licensed medical practitioner
what does ASA stand for?
aspirin
what does APAP stand for?
acetaminophen
what does aa qs stand for?
of each to make a sufficient quanity
commonly used verbs for SIG interpretation
take
inhale
give
place
instill
unwrap and insert
always use ________ measuring devices
calibrated
how do you use BSA?
find patient weight and height and connect with straight line— see where the line crosses in the middle
what is drug dosage based on?
age and weight
when is BSA used?
chemotherapy
pediatric patients
burn patients
what is a legend drug?
a prescription drug
drugs considered useful only after expert diagnosis OR too dangerous for use in self medication are made available upon the prescription of a licensed requirement
called “legend” bc it is a req that the label has the legend: “caution: federal law prohibits dispensing without a prescription”, Rx only, or similar phrase
how are prescriptions to be transmitted and received in Ohio?
a pharmacist may receive a signed hard copy prescription, an oral prescription, a facsimile of a signed prescription, or a prescription sent using a board approved electronic prescription transmission system
what info is required in a prescription?
full name & address of patient
date of issue
name and address of prescriber
name, strength, dosage form, and quantity of drug product prescribed
directions for use
number of refills
prescriber’s signature
required info for prescription label
name, address, and phone # of pharmacy
name of patient
name of prescriber
prescription number
date dispensed
initials of dispensing RPh
name, strength, and quantity of drug product dispensed
name of manufacturer or NDC number
beyond-use date
directions for use
examples of auxiliary labels
shake well
keep in refrigerator, do not freeze
don’t use after:
refrigerate, shake well, discard after:
protect from light
external use only
may cause drowsiness
avoid sun exposure
don’t drink alcohol
take with food
take on an empty stomach
take w full glass of water
finish all medication
compounded in this pharmacy
OTC drugs
drugs deemed safe enough for a layman in self-treatment of simple conditions for which competent medical care is not generally sought
controlled substances
drugs or other substances that have been deemed to have the potential for abuse or psychological/physical dependence
5 schedules
req special labeling
drug package will bear a schedule symbol such as C-II, C-III, etc.
federal transfer label states: federal law prohibits the transfer of this drug to any person other than the patient for whom it was prescribed
Schedule I (C-I)
no accepted medical use
high potetial for abuse
schedule II (C-II)
accepted medical uses
high potential for abuse
severe physiological and pysical dependence
schedule III (C-III)
accepted medical uses
lesser degree of abuse potential than C-II
moderate dependence
schedule IV (C-IV)
accepted medical uses
low potential for abuse relative to C-III
limited dependence
schedule V (C-V)
accepted medical uses
low potential for abuse relative to C-IV
limited dependence
how do you verify a prescriber’s DEA?
letters at beginning for prescribers are A, B, or F
second letter is the 1st letter of the prescriber’s last name
7 digit positions
for positions 1-6, calculate [sum of values in odd positions] + 2*[sum of values in even positions]
when is DEA # required?
when writing for a controlled substance
general labeling guidelines for liquids for oral administration unless otherwise stated
labeled in terms of each 5 mL portion
ex. ibuprofen 100mg/5mL
general labeling guidelines for capsules, tablets, or other unit dose forms such as suppositories
labeled to express the quantity of each therapeutically active ingredient contained in each unit
general labeling guidelines for topical semisolid dosage forms
labeled to express the w/w% concentration of each therapeutically active agent in the preparation
general labeling guidelines for liquid dosage forms that aren’t for oral delivery
various ways to label:
w/v% concentration
amt per mL, or some other specified volume
v/v% concentration
of each therapeutically active agent in the preparation
the concentration and dosage of electrolytes are often stated on the label in __________
milliequivalent (mEq)
beyond use date should be included in the labeling of _________ products
compounded
define beyond use date (BUD)
date placed on dispensing container by the PHARMACIST; date after which it should not be used
should not be later tan the expiration date on the manufacturer’s container
what is the longest BUD in Ohio?
1 year
do pharmacists assign expiration date or BUD?
BUD
manufacturer determines expiration date
what does D.A.W. stand for?
dispense as written