Idaho Admin. Code r. 24.36.01.011 - DEFINITIONS AND ABBREVIATIONS (O - Z)
The definitions set forth in Sections 54-1705 and 37-2701, Idaho Code, are applicable to these rules. In addition, the following terms have the meanings set forth below: (3-28-23)
01.
Parenteral Admixture . The preparation and labeling of sterile
products intended for administration by injection. (3-28-23)
02.
Pharmaceutical Care
Services. A broad range of services, activities and responsibilities
intended to optimize drug-related therapeutic outcomes for patients consistent
with Rule 100. Pharmaceutical care services
may be performed independent of, or concurrently with, the dispensing or
administration of a drug or device and also encompasses services provided by
way of DTM under a collaborative practice agreement. Pharmaceutical care
services are not limited to, but may include one (1) or more of the following:
(3-28-23)
a. Performing or obtaining necessary
assessments of the patient's health status, including the performance of health
screening activities or testing; (3-28-23)
b. Reviewing, analyzing, evaluating,
formulating or providing a drug utilization plan; (3-28-23)
c. Monitoring and evaluating the patient's
response to drug therapy, including safety and effectiveness;
(3-28-23)
d. Coordinating and
integrating pharmaceutical care services within the broader health care
management services being provided to the patient; (3-28-23)
e. Ordering and interpreting laboratory
tests; (3-28-23)
f. Performing drug
product selection, substitution, prescription adaptation, or refill
authorization as provided in these rules; and (3-28-23)
g. Prescribing drugs and devices as provided
in these rules. (3-28-23)
03.
PDMP . Prescription Drug
Monitoring Program. (3-28-23)
04.
Prescriber . An individual currently licensed, registered, or
otherwise authorized to prescribe and administer drugs in the course of
professional practice. (3-28-23)
05.
Purple Book . The list of
licensed biological products with reference product exclusivity and
biosimilarity or interchangeability evaluations published by the FDA under the
Public Health Service Act. (3-28-23)
06.
Readily Retrievable . Records
are considered readily retrievable if they are able to be completely and
legibly produced upon request within seventy-two (72) hours.
(3-28-23)
07.
Reconstitution . The process of adding a diluent to a powdered
medication to prepare a solution or suspension, according to the product's
labeling or the manufacturer's instructions. (3-28-23)
08.
Restricted Drug Storage
Area. The area of a drug outlet where prescription drugs are prepared,
compounded, distributed, dispensed, or stored. (3-28-23)
09.
Therapeutic Equivalent
Drugs. Products assigned an "A" code by the FDA in the Approved Drug
Products with Therapeutic Equivalence Evaluations (Orange Book) and animal drug
products published in the FDA Approved Animal Drug Products (Green Book).
(3-28-23)
10.
USP-NF .
United State Pharmacopeia-National Formulary. (3-28-23)
Notes
State regulations are updated quarterly; we currently have two versions available. Below is a comparison between our most recent version and the prior quarterly release. More comparison features will be added as we have more versions to compare.
No prior version found.