Compounding

Front 1

Personnel hand hygiene and garbing procedures should take place in the _

Back 1

Ante area

Front 2

What is ante area

Back 2

room in close proximity to the cleanroom where technicians perform support tasks, such as hand hygiene and garbing, staging of components, order entry, or labeling. It is typically equipped with sinks, cabinets, and benches. This room can be engineered as an ISO 8 or cleaner environment.

Front 3

All interior working surfaces of a laminar flow hood should be cleaned with

Back 3

70% isopropyl alcohol

Front 4

The required air quality for an ante-area is

Back 4

ISO 8

allows 3,520,000 particles per cubic meter.

Front 5

ISO means and purpose

Back 5

International Organization of Standardization

classifies air quality based on the number of particles 0.5 microns and larger per cubic meter.

Front 6

The required air quality for a buffer area is

Back 6

ISO 7

ISO Class 7 allows 352,000 particles per cubic meter.

Front 7

correct order of donning personal protective equipment when in the ante-area

Back 7

don shoe covers, don head and facial hair covers, don face mask, wash hands and forearms, and don a non-shedding gown.

Front 8

beyond-use date for a medium-risk compounded sterile product stored at room temperature cannot exceed

Back 8

30hrs

Front 9

set of specific instructions for making a compounded product.

Back 9

Master formula

Front 10

beyond-use date for a low-risk compounded sterile product stored at room temperature cannot exceed

Back 10

48hrs

Front 11

defined by USP 797 as the date and time after which a compounded sterile product (CSP) may not be stored or transported and is calculated from the date and time of compounding.

Back 11

BUD Beyond Use Date

Front 12

According to USP <795>, the beyond-use date for solids and non-aqueous liquids prepared from bulk ingredients is __in the absence of other data.

Back 12

6months

Front 13

1quart = __ml

Back 13

946ml

Front 14

When compounding capsules, powders, lozenges, or tablets, the weight of each finished unit should be between

Back 14

90-110%

Front 15

examples of incompatibility that can occur when compounding IV therapy.

Back 15

,Phase separation, turbidity, and precipitate formation

Front 16

According to USP <795>, the beyond-use date for compounded water-containing formulations is ___when stored under refrigeration in the absence of other data.

Back 16

14 day

Front 17

Type of Base:

-whiite petrolatum (vaseline)

Back 17

Oleaginous

Front 18

Type of base:

Velvachor

Back 18

oil/water emulsion ointment base,

Front 19

Type of base:

Aquaphor

Back 19

absorption ointment base,

Front 20

Type of base:

Eucerin

Back 20

W/O

Front 21

T or F:

Sterile water for injection USP does not contain antimicrobial agents.

Back 21

True

Front 22

T or F:

Conical graduates are less accurate for measuring liquids than cylindrical graduates.

Back 22

True

Front 23

When compounding emulsions, solutions, and suspensions, the weight of each filled container (corrected for tare weight), should be between

Back 23

100% and 110%

Front 24

__syringes must be used whenever possible for manipulating hazardous drugs.

Back 24

Luer-Lok

Front 25

types of water is used to reconstitute oral products?

Back 25

Purified water USP

Front 26

bases that are commonly used when compounding suppositories.

Back 26

Cocoa butter, hydrogenated vegetable oils, and glycerin

Front 27

An ampule requires the use of a __ needle.

Back 27

Filter needle

Front 28

Type of base:

Rose Water

Back 28

W/O

Front 29

When preparing a nonhazardous medication, which of the following syringe sizes should be selected?

Back 29

syringe size closest to the volume being measured

Front 30

Water cannot be used when compounding a sterile preparation.

Back 30

Purified water USP

Front 31

When measuring a liquid, the substance should not constitute less than ______________ of the graduate’s capacity.

Back 31

20%

Front 32

minimum weighable quantity that can be measured using a Class III prescription balance.

Back 32

120mg

Front 33

devices should be used when measuring a viscous substance?

Back 33

Syringes

Front 34

bases are suitable to use for drugs that are hydrolyzed by water. Why?

Back 34

Oleaginous

Oleaginous ointment bases are anhydrous and hydrophobic, making them good vehicles for hydrolyzable drugs.

Front 35

A __ gauge needle would be the least likely to cause coring among the needle sizes listed.

Back 35

26 gauge (bigger no compared to other choices

Front 36

Describbe the comparison between syringes gauge and their needle

Back 36

the higher the gauge number, the thinner the needle

Front 37

can be used to find the solubility of a drug in a particular solvent when compounding.

Back 37

Remington

Front 38

When preparing a hazardous medication, the measured volume should not exceed ______________ capacity of the syringe.

Back 38

75%

Front 39

The volume of fluid to be removed from a vial should be replaced with an ____ volume of air before withdrawing the fluid to prevent creating a vacuum.

Back 39

Equal

Front 40

appropriate compounding tool to use when mixing powders.

Back 40

wedgewood mortar

Front 41

appropriate to use when compounding an oral preparation requiring alcohol.

Back 41

95% ethyl alcohol

Front 42

To ensure fluid transfer into an IV bag, a needle that is greater than _____________ should be used to pierce the injection port.

Back 42

greater than 3/8-inches

Front 43

Mixing liquids and semisoft dosage forms is best done using

Back 43

glass mortar and pestle.

Front 44

To maintain sterility while compounding, the ______________ of a syringe should never be touched.

Back 44

Tip & ,plunger

Front 45

Sterile products are prepared in

Back 45

primary engineering control (PEC).

Front 46

To prevent contamination, all manipulations should be performed at least ______________ inside a laminar flow hood.

Back 46

6inches

Front 47

______ filter should be used to sterilize ophthalmic solutions.

Back 47

0.22micron

Front 48

technique used when compounding suspensions.

Back 48

Lwvigation

Front 49

What is Levigation

Back 49

the process of grinding an insoluble substance to a fine powder, while wet. The material is introduced into the mill together with water, in which the powdered substance remains suspended, and flows from the mill as a turbid liquid or thin paste, according to the amount of water employed. This method is used to reduce the particle size of insoluble materials when compounding ointments and suspensions.

Front 50

T/F

Needle shafts should never be swabbed with 70% isopropyl alcohol or touched prior to use for a sterile preparation.

Back 50

True