The Beginning
What publication attributed to Ancient Rome was used by medical professionals as late as the 16th century.
What is the De Materia Medica.
How are prescriptions organized in the to-be-filled section of the data entry area.
What is by pick-up times.
Why did the National Association of Boards of Pharmacy (NABP) implement CPE Monitor.
What is to maintain a repository for continuing education documentation.
Which online references providers formulary management and cost containment information, including wholesale price information for brand-name and generic medications.
What is the Red Book.
Description of an FDA Class I medication recall.
What is a dangerous or defective product that could cause serious health problems or death.
This is the name of the first official pharmacopeia followed by European apothecaries in the 15th century.
What is Nuovo Receptario.
Name the 3 sections of the pharmacy counter.
What is the in-window, out-window and counseling areas.
How are professionals standards different from statutes and regulations.
What is professional standards are set forth by the profession but, unlike statutes and regulations, are not enforceable by law.
Which references contains many facts about medication product groups and individual products and makes comparisons among them.
What is the Drug Fact and Comparisons.
Description of an FDA Class II medication recall.
What is a product that might cause a temporary health problem or pose a slight threat of a serious nature.
What ancient Chinese document listed the medicinal value of hundreds of herbs.
What is the Pen T-Sao Documents.
What are the 3 functional components/sections of the data entry area.
What are the to-be-entered section, the to-be-filled section & the staging section.
What is the primary role of a state board of pharmacy.
What is to regulate the operation of pharmacy departments, the practice of pharmacy by pharmacists & the performance of technical functions by pharmacy technicians.
Why did the National Association of Boards of Pharmacy (NABP) implement CPE Monitor.
What is to maintain a repository for continuing education documentation.
Description of an FDA Class III medication recall.
What is a product is unlikely to cause any adverse health reaction, but that violates FDA labeling or manufacturing laws.
What is the Papyrus Ebers.
What is an ancient Egyptian collection of 800 prescriptions that mentions 700 medications.
Which items are placed in the staging section of the data entry area.
What are the label, the original prescription order & stock bottles of medication to dispense.
What is the Food, drug and Cosmetic Act of 1938.
What is a law that was enacted to ensure that all medications are pure and safe ad that resulted in the creation of the Food and Drug Administration (FDA).
Which publication is considered the gold standard reference on self-care and over-the-counter (OTC) medications?
What is the Handbook of Nonprescription Drugs.
This public safety information about mediations distributed to the medical community and public by the FDA. What is safety alerts, recalls, withdrawals & important labeling changes.
What is safety alerts, recalls, withdrawals & important labeling changes.
What was the Master, Wardens and Society of the Art and Mystery of the Apothecaries of the City of London.
What is the 1st organization of pharmacists established in 1617.
Which types of products are made in the compounding area.
What are nonsterile products such as creams, ointments, lotion & gels.
Define The Durham-Humphrey amendment of 1951.
What is a piece of legislation that distinguished prescription medications from over-the-counter (OTC) medications by requiring adequate directions for use unless the medication contains the federal legend statement.
Name 3 online sources for medication information, medication management and disease management.
What is - Micromedex, Lexicomp Online & Epocrates Online.
Name 3 courses of action the FDA CAN TAKE IF IT DETERMINES A MEDICATION PRESENTS A RISK OF ILLNESS, INJURY OR CONSUMER DECEPTION.
What are seize the medication, issue a recall & seek an injunction to prevent the manufacturer from distributing the medication.