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USP <795>
Nonsterile compounding
USP <797>
Sterile compounding
USP <800>
Hazardous-drug handling
Aseptic technique
Practices intended to minimize contamination of sterile preparations
Critical site
A surface/opening that can directly contact sterile product or fluid pathway and must remain sterile
Example of critical site
Syringe tip
Trituration
Grinding a powder to reduce particle size
Levigation
Mixing powder with a small amount of suitable liquid to form a smooth paste/reduce particle size
Geometric dilution
Gradually mixing small amounts of a potent ingredient with increasing amounts of diluent
BUD
Beyond-use date for a compounded preparation
BUD vs expiration date
BUD is assigned to a compounded preparation; manufacturer expiration applies to commercially manufactured product
Reconstitution
Adding specified diluent to a powder/concentrate to produce the intended final preparation
Amount of water used to reconstitute an antibiotic
Use manufacturer's specified amount/instructions
Why don't you simply add water equal to final bottle volume?
Powder occupies volume; manufacturer specifies diluent necessary for correct final concentration
LASA
Look-alike/sound-alike
Tall Man lettering
Emphasizes differing parts of similar drug names to prevent medication errors
Near miss
Medication error caught before reaching the patient
Class I recall
Reasonable probability of serious adverse consequences or death
Class II recall
Temporary/reversible consequences or remote probability of serious consequences
Class III recall
Unlikely to cause adverse health consequences
FEFO
First expire, first out
Purpose of FEFO
Use products with earlier expiration dates first when appropriate
Recalled product on shelf
Quarantine/remove according to recall procedure
Possible cold-chain excursion
Quarantine product and alert pharmacist/follow procedure
Typical refrigerator range
2–8°C
Lot number
Identifies a specific manufacturing batch
Why are lot numbers important?
Recalls and product traceability
Formulary
List of drugs covered/preferred by a health plan
Prior authorization
Insurer requires additional approval/information before covering medication
Refill-too-soon rejection
Insurance believes medication is being refilled before allowable date/expected use period
BIN
Identifies the processor/routing information used in pharmacy claims
PCN
Processor Control Number; further routes/identifies pharmacy benefit claims
Group number
Identifies patient's benefit group/plan grouping
Member ID
Identifies the individual insured member
PHI
Protected Health Information
Medication Guide
FDA-required patient information for certain medications with serious/significant risks
REMS
Risk Evaluation and Mitigation Strategy
REMS purpose
Ensure benefits of certain drugs outweigh serious risks
Final clinical verification
Pharmacist responsibility
Technician independently changes prescribed dose?
No
Technician independently recommends therapy to patient?
No; refer clinical decisions/counseling to pharmacist
Best response when you're unsure whether a pharmacy task is within technician scope
Stop and ask the pharmacist/follow applicable law and policy