Ch 61 A 11 Pharmacy Flashcards
Administer
The direct application of a drug to the body of a patient or research subject by injection, inhalation, ingestion or any other means as a result of an order of a licensed practitioner
Board
The board of pharmacy
Compounding
Preparing, mixing, assembling, packaging or labeling a drug or device as the result of a licensed practitioner’s prescription or for the purpose of, or as an incident to, research, teaching or chemical analysis and not for sale or dispensing. Also includes preparing drugs or devices in anticipation of a prescription based on routine, regularly observed prescribing patterns
Confidential information
Information in the patient’s pharmacy records accessed, maintained by or transmitted to the pharmacist or communicated to the patient as part of patient counseling and may be released only to the patient or as the patient directs; or to those licensed practitioners and other authorized health care professionals as defined by regulation of the board when, in the pharmacist’s professional judgment, such release is necessary to protect the patient’s health and well-being; or to other persons authorized by law to receive the information, regardless of whether the information is on paper, preserved on microfilm or stored on electronic media;
Consulting pharmacist
A pharmacist whose services are engaged on a routine basis by a hospital or other health care facility and who is responsible for the distribution, receipt and storage of drugs according to the state and federal regulations
Custodial care facility
A nursing home, retirement care, mental care or other facility that provides extended health care
Dangerous drug
A drug that is required by an applicable federal or state law or rule to be dispensed pursuant to a prescription or is restricted to use by licensed practitioners; or that is required by federal law to be labeled with any of the following statements prior to being dispensed or delivered:
(1) “Caution: federal law prohibits dispensing without prescription.”;
(2) “Caution: federal law restricts this drug to use by or on the order of a licensed veterinarian.”; or
(3) “RX only”;
Device
An instrument, apparatus, implement, machine, contrivance, implant or similar or related article, including a component part or accessory, that is required by federal law to bear the label, “Caution: federal or state law requires dispensing by or on the order of a physician.”
Dispense
The evaluation and implementation of a prescription, including the preparation and delivery of a drug or device to a patient or patient’s agent in a suitable container appropriately labeled for subsequent administration to or use by a patient
Distribute
The delivery of a drug or device other than by administering or dispensing
Drug
(1) an article recognized as a drug in an official compendium or its supplement that is designated from time to time by the board for use in the diagnosis, cure, mitigation, treatment or prevention of disease in humans or other animals;
(2) an article intended for use in the diagnosis, cure, mitigation, treatment or prevention of diseases in humans or other animals;
(3) an article, other than food, that affects the structure or a function of the body of humans or other animals; and
(4) an article intended for use as a component of an article described in Paragraph (1), (2) or (3) of this subsection
Drug regimen review
An evaluation of a prescription and patient record for:
(1) known allergies;
(2) rational therapy contraindications;
(3) reasonable dose and route of administration;
(4) reasonable directions for use;
(5) duplication of therapy;
(6) drug-drug interactions;
(7) adverse drug reactions; and
(8) proper use and optimum therapeutic outcomes;
Pharmacy Intern
A person licensed by the board to train under a pharmacist
Hospital
An institution that is licensed as a hospital by the department of health
Labeling
The process of preparing and affixing a label to a drug container exclusive of the labeling by a manufacturer, packer or distributor of a nonprescription drug or commercially packaged prescription drug or device; and which label includes all information required by federal or state law or regulations adopted pursuant to federal or state law