Card Set Information
Chapter 15 pharmacy
A sterile, injectable medication; introduction of a drug or nutrient into a vein, muscle, subcutaneous tissue, artery, or spinal column; often refers to intravenous infusions of nutritional solutions.
Free from microorganisms
Compound Sterile Preparation (CSP)
relates to the compounding of sterile preparations, including intravenous admixtures, ophthalmics, intrathecals, etc., prepared in a controlled sterile environment
Within a vein; administered drugs or fluids directly into the vein to obtain a rapid or complete effect from the drug.
The administration of an IV infusion over a period of time followed by a period of no administration. Same cycle usually is repeated at sceduled times, hence the name intermittance
within the muscle
Under the skin
situated or applied within the skin
the injection of a sterile preparation
the injection of a sterile preparation in a joint such as the elbow or knee.
the injection of a sterile preparation directly into the heart
a sterile preparation is injected into the peritoneal or abdominal cavity
a sterile preparation is injected into the sac surrounding the lungs.
The injection into a ventricle of the brain or heart.
a preparation instilled into the urinary bladder
A sterile preparation is injected into the vitrenous chamber of the eyeball behind the lens
within the subdural space of the spinal cord
an ISO Class 8 or better area where personnel perform hand hygiene and garbing procedures. Staging of components, order entry, CSP labeling and other high-particulate generating activities
the term used to denote one or more active ingredients in a large volume parenteral solution
a method to assure that no contamination of compounded sterile products will occur during their compounding.
a method of preparation that will prevent contamination of a site (e.g. wound) or product (e.g. IV admixture).
usually an ISO class 7 area where the laminar flow hood is located.
an ISO class 5 area
any opening or surface that can provide a pathway between the sterile product and the environment.
Direct compound area
a critical compounding area meeting ISO 5 specifications
Having a higher osmotic pressure than a reference solution, usually refer to blood plasma or lacrimal fluid.
having a lesser osmotic pressure than a reference standard, usually refering to blood plasma or lacrimal fluid
ISO class 5 area
International organization of standardization (ISO) Classification of particulate matter in room air, with no more than 3,520 particles per cubic meter of air 0.5 microns and larger.
ISO class 7 area
International Organization of Standardization (ISO) Classification of particulate Matter in room air, with no more than 352,000 particles per cubic meter of air 0.5 microns or larger.
ISO class 8 area
International organization of Standardization (ISO) Classification of Particulate Matter in room air, with no more than 3,520, 000 particles per cubic meter of air 0.5 microns and larger.
primary engineering control (PEC)
a device such as a laminar flow workbench, biological safety cabinet, or compounding aseptic isolator, which provides the ISO class 5 environment necessary for compounding sterile preparations
the filters used to sieve, absorb, and entrap, foreign particles to achieve sterilization.
the air flow moving in a single direction in a robust and uniform manner to sweep particles away from the critical processing area related to laminar air flow.
a proof or confirmation of validity
the confirmation of a truth or fact
When working in a horizontal laminar airflow hood, you must work at least _________ from the outside edge to the work surface.
Which of the ISO classifications listed below is equvilant to a class 100 area?
ISO class 5
When working in a laminar flow hood
You must protect all critical sites by never putting your hand or object between the critical site and the hepa filtered air.
In the definition of class 100, class 10, 000, and class 100, 000 rooms, we are always talking about total particles________microns in size or larger
A tubercolin skin test is given by which route or administration
The compunding of a total parenteral nutrition solution could be an example of
Medium risk level compounding
When choosing a sterilizing filter must be considered
The volume of the product to be filtered
the compatability of the membrane of the product to be filtered
whether the solution to be filtered is hydrophobic or hydrophilic
The pore size of a sterilizing filter is?
A sterile product is one that is
free from all living microorganisms
An operator must successfully complete one media fill before compounding any sterile products
correct USP media transfers
Choose the most correct answer about transfering products into the antearea
bottles, bags, and syringes must be removed from brown card board boxes before being brought into the antearea
please choose the most correct conclusion to the statement; the plenum in a lamianar flow workbench is
An area where air is pressurized for distribution over the hepa-filter