DDS Flashcards

1
Q

A mixture of finely divided drugs or chemical in dry form; may be used internally or externally

A

Powder

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2
Q

8 sieve

A

Very coarse

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3
Q

20 sieve

A

Coarse

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4
Q

40 sieve

A

mod. Coarse

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5
Q

60 sieve

A

Fine

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6
Q

80 sieve

A

Very fine

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7
Q

The process of reducing the particle size of a solid substance to a finer state of subdivision.

A

Comminution

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8
Q

Substance is reduced to small particles by rubbing it in a mortar and pestle.

Trituration
Levigation
Pulverization by Intervention

A

Trituration

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9
Q

Substances are reduced and subdivided with an addition of material (ex. Solvent) that is easily removed after pulverization.

Trituration
Levigation
Pulverization by Intervention

A

Pulverization by Intervention

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10
Q

The particle size of the substance is reduced by adding a suitable nonsolvent to form a paste.

Trituration
Levigation
Pulverization by Intervention

A

Levigation

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11
Q

Common levigating agent

A

Mineral Oil

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12
Q

spatula is used to blend small amounts of powders on a sheet of paper or a pill tile.

Geometric dilution
Trituration
Tumbling
Spatulation
Sifting

A

Spatulation

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13
Q

mortar and pestle is used to reduce substance to small particles

Geometric dilution
Trituration
Tumbling
Spatulation
Sifting

A

Trituration

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14
Q

used when potent substances must be mixed with a large amount of diluent.

Geometric dilution
Trituration
Tumbling
Spatulation
Sifting

A

Geometric dilution

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15
Q

powders are mixed by passing them through sifters similar to those used to sift flour.

Geometric dilution
Trituration
Tumbling
Spatulation
Sifting

A

Sifting

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16
Q

the process of mixing powders in a large container rotated by a motorized process

Geometric dilution
Trituration
Tumbling
Spatulation
Sifting

A

Tumbling

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17
Q

Intended to be administered in dosage quantities that are
safe for the patient to measure.
Should pass through a 100-mesh sieve.
Dusting powders, aerosols, dentifrices, antacids, laxatives,
dietary nutrient supplements, douches

Bulk Powders
Divided Powders
Dusting Powders

A

Bulk Powders

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18
Q

Must be homogenous, free from potential of causing local
irritation.
Should flow easily, spread uniformly, and cling to the skin
upon application.
Generally dispensed in sifter-top containers

Bulk Powders
Divided Powders
Dusting Powders

A

Dusting Powders

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19
Q

(chartula, charts, powder papers, powders).
Single doses of the powdered drug mixture individually
enclosed in paper, cellophane, or metallic foil wrappers or
packets.
Sufficiently potent to require premeasured doses.

Bulk Powders
Divided Powders
Dusting Powders

A

Divided Powders

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20
Q

moisture resistant

Vegetable parchment
White bond
Glassine
Waxed

A

Vegetable parchment

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21
Q

moisture resistant properties

Vegetable parchment
White bond
Glassine
Waxed

A

White bond

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22
Q

moisture resistant

Vegetable parchment
White bond
Glassine
Waxed

A

Glassine

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23
Q

transparent waterproof paper (double wrap w/
white bond paper for protection from moisture)

Vegetable parchment
White bond
Glassine
Waxed

A

Waxed

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24
Q

Not intended for use with potent drugs because of
inherent error when a patient measures the dose with a teaspoon, scoop, etc.
Good for unstable drugs
Example: antibiotics for reconstitution

A

Granules

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25
Contain mixtures of citric acid, tartaric acid, or sodium biphosphate with a bicarbonate and a medicinal agent.
Effervescent Granules
26
Examples of Effervescent Granules:
Lactinex, Bassoran, Zantac
27
a method in preparing granules were one molecule of water present in each molecule of citric acid acts as the binding agent for the powder mixture. Dry or Fusion Method Wet Method
Dry or Fusion Method
28
a method in preparing granules were the water added to alcohol is the moistening agent, forming the pliable mass of granulation Dry or Fusion Method Wet Method
Wet Method
29
Solid dosage forms in which one or more medicinal or inert substances are enclosed within a small gelatin shell.
CAPSULES
30
used in most commercial medicated capsules. They are commonly employed in clinical drug trials to compare the effects of an investigational drug with those of another drug product or placebo. Hard Gelatin Capsules Soft Gelatin Capsules
Hard Gelatin Capsules
31
made of gelatin to which glycerin or a polyhydric alcohol such as sorbitol has been added. They are used to encapsulate and hermetically seal liquids, suspensions, pasty materials, dry powders, and even formed tablets. Hard Gelatin Capsules Soft Gelatin Capsules
Soft Gelatin Capsules
32
smallest capsule size?
5
33
largest capsule size
000
34
How do automated and semi-automated capsule-filling equipment typically fill the capsule body with the formulation? a) Gravity fill b) Tamping c) Screw-feed mechanism d) All of the above
d) All of the above
35
Method that is commonly used to fill extemporaneously compounded capsules? a) Gravity fill b) Tamping c) Screw-feed mechanism d) Punch method
d) Punch method
36
Containers for Dispensing Capsules:
● Tight ● Well-closed ● Light-resistant
37
Most commonly used solid dosage form.
TABLETS
38
inert substances used to give a preparation a suitable form or consistency.
Excipients
39
Which physical features can compressed tablets have? a) Round, oblong, or unique in shape b) Thick or thin c) Large or small in diameter d) All of the above
d) All of the above
40
tablets that are prepared by subjecting the fill material to more than a single compression? a) Multiple Compressed Tablets b) Compressed tablets c) Sugarcoated tablets d) Film-coated tablets
a) Multiple Compressed Tablets
41
type of tablet coating that is water-soluble and quickly dissolves after swallowing? a) Sugarcoated tablets b) Film-coated tablets c) Gelatin-coated tablets d) Enteric-coated tablets
a) Sugarcoated tablets
42
primary advantage of film-coated tablets over sugar-coated tablets? a) Durability b) Quick dissolution after swallowing c) Less bulkiness d) Time-saving application process
c) Less bulkiness
43
type of tablet has a gelatin coating, allowing it to be smaller than a capsule filled with an equivalent amount of powder? a) Sugarcoated tablets b) Film-coated tablets c) Gelatin-coated tablets d) Enteric-coated tablets
c) Gelatin-coated tablets
44
purpose of enteric-coated tablets? a) To dissolve quickly after swallowing b) To be tamper-evident c) To bypass the stomach and release the drug in the intestines d) To provide rapid drug effects
c) To bypass the stomach and release the drug in the intestines
45
type of tablets that are intended to be dissolved in the buccal pouch or beneath the tongue for absorption through the oral mucosa? a) Sugarcoated tablets b) Film-coated tablets c) Buccal tablets d) Sublingual tablets e) c and d
e) c and d (Buccal and Sublingual Tablets)
46
compressed tablets coated with a thin layer of a polymer capable of forming a skin like film; it is more durable, less bulky, and less time-consuming to apply. a) Sugarcoated tablets b) Film-coated tablets c) Gelatin-coated tablets d) Enteric-coated tablets
b) Film-coated tablets
47
tablets that have delayed-release features. They are designed to pass unchanged through the stomach to the intestines, where the tablets disintegrate and allow drug dissolution and absorption and/or effect. a) Sugarcoated tablets b) Film-coated tablets c) Gelatin-coated tablets d) Enteric-coated tablets
d) Enteric-coated tablets
48
Tablets designed to erode slowly
Buccal tablets
49
Tablets designed to dissolve promptly and provide rapid drug effects.
Sublingual Tablets
50
general shape of lozenges or troches? a) Round b) Rectangular c) Disc-shaped d) Triangle
c) Disc-shaped
51
Lozenges or troches typically manufactured by? a) By compaction b) By compression or molding c) By encapsulation d) By lyophilization
b) By compression or molding
52
Type of tablet that has a smooth, rapid disintegration when chewed or dissolved in the mouth? a) Chewable tablets b) Effervescent tablets c) Molded tablets d) Tablet triturates
a) Chewable tablets
53
primary advantage of chewable tablets? a) Smooth and rapid disintegration b) Creamy base with flavored and colored mannitol c) Easy administration to children and individuals with difficulty swallowing d) Rapid dissolution and bubble action
c) Easy administration to children and individuals with difficulty swallowing
54
How are effervescent tablets prepared? a) By compression or molding b) By encapsulation c) By compaction d) By compressing granular effervescent salts
d) By compressing granular effervescent salts
55
How are effervescent tablets prepared? a) By compression or molding b) By encapsulation c) By compaction d) By compressing granular effervescent salts
d) By compressing granular effervescent salts
56
purpose of effervescent tablets? a) Smooth and rapid disintegration b) Creamy base with flavored and colored mannitol c) Rapid dissolution and bubble action d) Rapid release of highly potent drugs
c) Rapid dissolution and bubble action
57
type of tablets are used for rapid dissolution and are very soft and soluble? a) Chewable tablets b) Effervescent tablets c) Molded tablets d) Tablet triturates
c) Molded tablets
58
primary purpose of hypodermic tablets? a) Smooth and rapid disintegration b) Sublingual administration c) Parenteral preparation of solutions d) Dispensing accurate amounts of potent drugs
c) Parenteral preparation of solutions
59
purpose of dispensing tablets? a) Smooth and rapid disintegration b) Creamy base with flavored and colored mannitol c) Rapid dissolution and bubble action d) Rapidly obtaining premeasured amounts of highly potent drug substances
d) Rapidly obtaining premeasured amounts of highly potent drug substances
60
Designed to disintegrate and release their medication with no special rate-controlling features, such as special coatings and other techniques. Immediate-Release Tablets Extended-Release Tablets
Immediate-Release Tablets
61
Characterized by disintegrating or dissolving in the mouth within 1 minute, some within 10 seconds (e.g., Claritin Reditabs [loratadine]). Liquefy on the tongue, and the patient swallows the liquid.
Rapidly Disintegrating or Dissolving Tablets
62
Sometimes called controlled release. Designed to release their medication in a predetermined manner over an extended period. Immediate-Release Tablets Extended-Release Tablets
Extended-Release Tablets
63
a.k.a Vaginal inserts ● Generally compressed tablets for vaginal administration ● Treatment of vaginitis & vulvovaginitis candidiasis Lollipops Pills Vaginal Tablets
Vaginal Tablets
64
a raspberry lollipop that is a sugar-based lozenge on a stick and contains fentanyl citrate.
Fentanyl Actiq (Cephalon)
65
first product specifically designed to aid in controlling breakthrough pain in cancer patients. Its effects last for only about 15 minutes, but that is usually long enough to relieve the breakthrough pain.
Actiq
66
small, round solid dosage forms containing a medicinal agent and intended to be administered orally Lollipops Pills Vaginal Tablets
Pills
67
complete or partial separation of the top or bottom of the tablet from the main body.
Capping
68
separation of a tablet into 2 or more distinct layers
Lamination
69
disfiguration of the core tablet when subjected for too long to the coating solution
Tablet erosion
70
removal of materials from the surfaces of the tablet and adherence of the face of the punch.
Picking
71
formation of uneven or rough irregularities on the surface of a coating film applied on a core tablet surface
Peeling
72
where the surface of the applied film coating is extremely rough and nonglossy, often taking on the appearance of the skin of an orange
Orange peel effect
73
adhesion of the granulation to the die and/or the build up of materials on the punch faces.
Sticking
74
unequal color distribution on surface
Mottling
75
coating bridges formed across a logo or break line
Bridging
76
Solid masses inserted into body cavities in which they will melt at body temperature or dissolve into aqueous secretions of body orifice.
Suppositories
77
Bullet, torpedo
Rectal
78
Globular, ovoid, cone
Vaginal
79
Pencil- Like
Urethral
80
Suppositories for Local & Systemic
Rectal
81
Suppositories for Local only
Vaginal & Urethral
82
Ovoid tablets inserted into the vagina using a plastic inserter; contains antimicrobial agents. Vaginal Tablets/ Inserts Implants/ Pellets
Vaginal Tablets/ Inserts
83
Small, sterile cylinders or devices inserted under the skin for prolonged and continuous absorption. Vaginal Tablets/ Inserts Implants/ Pellets
Implants/ Pellets
84
Petrolatum, USP
Yellow Petrolatum or Petroleum Jelly (Vaseline)
85
White Petrolatum, USP
Decolorized Petrolatum (White Vaseline)
86
Yellow Ointment, USP
(Simple ointment)
87
has an emollient effect protect against the escape of moisture as occlusive dressings immiscible with water (difficult to wash off) Absorption Bases Water-Soluble Base Water-Removable Base Oleaginous or Hydrocarbon Base
Oleaginous or Hydrocarbon Base
88
used as emollients not easily removed from the skin Absorption Bases Water-Soluble Base Water-Removable Base Oleaginous or Hydrocarbon Base
Absorption Bases
89
O/W emulsion commonly known as Creams. easily washed off /water-washable base Absorption Bases Water-Soluble Base Water-Removable Base Oleaginous or Hydrocarbon Base
Water-Removable Base
90
do not contain oleaginous base water-washable, greaseless use for incorporation of solid substances Absorption Bases Water-Soluble Base Water-Removable Base Oleaginous or Hydrocarbon Base
Water-Soluble Base
91
components are combined by melting and cooled with constant stirring until congealed. heat-labile and volatile constituents added last. conducted in porcelain dish or glass. beaker (small scale) Incorporation Fusion
Fusion
92
large steam jacketed kettles (large scale). use low temperature in melting materials with high melting point Incorporation Fusion
Fusion
93
Mortar and pestle Pill tile and spatula Ointment mill Incorporation Fusion
Incorporation
94
Unguator Incorporation of solids Incorporation of liquid Incorporation Fusion
Incorporation
95
semisolid preparations containing one or more medicinal agents dissolved or dispersed in either a W/O emulsion or O/W emulsion or in another type of water-washable base. Gels Creams Ointments
Creams
96
Semisolid systems consisting of dispersions of small or large molecules in an aqueous liquid vehicle rendered jelly-like through the addition of a gelling agent Gels Creams Ointments
Gels
97
Semisolid preparations intended for external application to the skin or mucous membranes that soften or melt at body temperature. Gels Creams Ointments
Ointments
98
(carbomer 934) belongs to what type of Gelling agent? cellulose derivatives synthetic macromolecules natural gums
synthetic macromolecules
99
carboxymethyl cellulose or hydroxypropyl methyl cellulose belongs to what type of Gelling agent? cellulose derivatives synthetic macromolecules natural gums
cellulose derivatives
100
tragacanth belongs to what type of Gelling agent? cellulose derivatives synthetic macromolecules natural gums
natural gums
101
Gels in which the macromolecules are uniformly distributed throughout a liquid with no apparent boundaries between the dispersed macromolecules and the liquid Single Phase Two Phase
Single Phase
102
When the gel mass consists of floccules of small distinct particles (magmas) Single Phase Two Phase
Two Phase
103
Usually involve organics Single Phase Two Phase
Single Phase
104
Usually involve inorganics Single Phase Two Phase
Two Phase
105
alcohol or Propylene glycol in gels are?
Solvents
106
methylparaben, propylparaben, chlorhexidine gluconate in gels are?
Antimicrobial preservative
107
Edetate disodium in gels are?
Stabilizer
108
When the interaction between particles of the dispersed phase becomes so great that on standing, the dispersing medium is squeezed out in droplets and the gel shrinks.
Syneresis
109
The taking up of a certain amount of liquid without a measurable increase in volume
Imbibition
110
A reversible gel-sol formation with no change in volume or temperature
Thixotropy
111
The taking up of liquid by a gel with an increase in volume
Swelling
112
Controlled release DDS or patches which allow the passage of drugs from the skin to the systemic circulation
TRANSDERMAL PREPARATION
113
generally, contain a larger proportion of solid material (such as 25%) than ointments and therefore are stiffer. Pastes Plasters
Pastes
114
solid or semisolid adhesive masses spread on a backing of paper, fabric, moleskin, or plastic. The adhesive material is a rubber base or a synthetic resin. Applied to the skin to provide prolonged contact at the site. Pastes Plasters
Plasters
115
are plastic masses containing gelatin (15%), glycerin (40%), water (35%), and an added medicinal substance (10%), such as zinc oxide.
Glycerogelatins
116
use in varicose ulcers
Zinc Gelatin
117
Aqueous preparations with insoluble material for external application without friction CERATES SOLUTIONS LOTIONS
LOTIONS
118
Semisolid preparations containing a relatively high wax content. Not to be directly rubbed onto skin; used as skin protectants before. CERATES SOLUTIONS LOTIONS
CERATES
119
prevents water loss and drug loss Adhesive Layer Occlusive Backing Layer Drug Matrix System Release Liner
Occlusive Backing Layer
120
stores API Adhesive Layer Occlusive Backing Layer Drug Matrix System Release Liner
Drug Matrix System
121
ensures continuous drug absorption Adhesive Layer Occlusive Backing Layer Drug Matrix System Release Liner
Adhesive Layer
122
removed before use to enable drug release Adhesive Layer Occlusive Backing Layer Drug Matrix System Release Liner
Release Liner
123
1st TDDS developed; for motion sickness
Scopolamine (Transderm Scop)
124
Ux for angina
Nitroglycerin
125
Ux for angina
Nitroglycerin
126
1st TDDS for hypertension
Clonidine
127
opioid analgesic
Fentanyl
128
hormone replacement therapy
Estradiol and Testosterone
129
Liquid preparations containing one or more drug substances that are molecularly dispersed in a suitable solvent or a mixture of mutually miscible solvents One of the oldest dosage forms known
SOLUTIONS
130
most useful solvent in pharmacy
water
131
2nd most useful solvent in pharmacy
Alcohol, US
132
absolute alcohol; NLT 99.5% by vol.
Dehydrated Alcohol, USP
133
Prepared by mixing equal volumes of Alcohol, USP and Purified Water, USP. Useful hydroalcoholic solvent
Diluted Alcohol, NF
134
Clear syrupy liquid with a sweet taste, miscible in both water and alcohol
Glycerin, USP
135
Viscous liquid miscible with water and alcohol. Frequently substituted for glycerin in modern pharmaceutical formulations
Propylene Glycol, USP
136
This and 91% isopropyl alcohol soln are commonly employed by diabetic pxs in preparing needles and syringes for hypodermic injections of insulin & for skin disinfection
Isopropyl Rubbing Alcohol
137
Has fewer solid impurities than ordinary drinking water. ● When evaporated to dryness, it must not yield more than 0.001% of residue. ● Used in the preparation of aqueous dosage forms except those intended to be administered parenterally
Purified Water, USP
138
Effective in treating patients with mild volume depletion (5%-10% of BW) Oral Solution Dry Mixtures for Solutions Oral Colonic Lavage Solution Oral Rehydration Solutions
Oral Rehydration Solutions
139
For medicinal agents, especially antibiotics, that have insufficient stability in aqueous solutions Oral Solution Dry Mixtures for Solutions Oral Colonic Lavage Solution Oral Rehydration Solutions
Dry Mixtures for Solutions
140
Can be dispensed as is or diluted to prepare a pediatric form Oral Solution Dry Mixtures for Solutions Oral Colonic Lavage Solution Oral Rehydration Solutions
Oral Solution
141
Alternative method of preparing the GIT of bowel for procedures, and requires less time and dietary restriction Oral Solution Dry Mixtures for Solutions Oral Colonic Lavage Solution Oral Rehydration Solutions
Oral Colonic Lavage Solution
142
Clear, sweetened, hydroalcoholic solutions that are usually flavored and are suitable for drugs that are insoluble in water alone but soluble in water–alcohol mixtures
ELIXIRS
143
Alcoholic or hydroalcoholic solutions of chemicals or soluble constituents of crude drugs
TINCTURES
144
Aqueous solution used for cleansing and maintaining acidic pH of vagina Spirits Diluted acids Aromatic waters Vaginal douches
Vaginal douches
145
clear, saturated or aqueous sol’ns of volatile oils or other aromatic substances Spirits Diluted acids Aromatic waters Vaginal douches
Aromatic waters
146
Aqueous solutions prepared by dissolving concentrated acids in water Diluted HCI (10% w/v) - Tx. gastric achlorhydria Spirits Diluted acids Aromatic waters Vaginal douches
Diluted acids
147
essences; hydroalcoholic sol’ns of volatile substances; highest alcohol content: ≥60% Spirits Diluted acids Aromatic waters Vaginal douches
Spirits
148
Alcoholic or oleaginous solutions (or emulsions) containing >1 API and are usually rubbed on the skin Salicylic acid collodion Flexible collodion Collodion/ Colloidion Liniments
Liniments
149
Clear or slightly opalescent viscous liquid, water repellent protective 4% pyroxylin + ether-alcohol mixture (3:1) Salicylic acid collodion Flexible collodion Collodion/ Colloidion Liniments
Collodion/ Colloidion
150
Colloidion + 3% Castor oil (for flexibility) and 2% Camphor (for waterproofing); topical protectant Salicylic acid collodion Flexible collodion Collodion/ Colloidion Liniments
Flexible collodion
151
Flexible collodion + 10% Salicylic acid; keratolytic Salicylic acid collodion Flexible collodion Collodion/ Colloidion Liniments
Salicylic acid collodion
152
fever-producing organic substances arising from microbial contamination
Pyrogens
153
earliest injectable drug to receive official recognition
Hypodermic morphine solution-
154
Most frequently used solvent in the large-scale manufacture of injections. Distillation or Reverse osmosis. NMT mg/100mL total solids and may not contain added substances; Pyrogen-free
Water for Injection, USP
155
In single-dose containers not larger than 1L. Pyrogen-free, endotoxin level: 0.25 USP EU/mL. 1L bottles not to be administered IV.
Sterile Water for Injection, USP
156
SWI with one or more suitable antimicrobials
Bacteriostatic Water for Injection, USP
157
Sterile isotonic solution of NaCl in WFI. No antimicrobials; 154mEq each of Na and Cl per liter
Sodium Chloride Injection, USP
158
Contains one or more suitable antimicrobial, and must be indicated on the label. <30mL containers
Bacteriostatic Sodium Chloride Injection, USP
159
Sterile solution of NaCl, KCl, and CaCl2 in WFI; Vehicle; electrolyte replenisher, plasma volume expander
Ringer’s Injection, USP
160
Different quantities of the chlorides + Na lactate. Fluid and electrolyte replenisher; systemic alkalizer
Lactated Ringer Injection, USP
161
the active principle of the pancreas gland, is primarily concerned with the metabolism of carbohydrates but also influences protein and fat metabolism.
Insulin
162
a buildup of fibrous tissue
lipohypertrophy
163
fat loss in small area of the body
lipodystrophy
164
From beef or pork pancreas or both U-100 or U-500. Colorless to straw-colored solution; substantially free from turbidity Only insulin that can be administered IV
Regular Insulin
165
Biosynthetic human insulin- first FDA approved rDNA drug product
Human Insulin (Humulin)
166
Recombinant rapid-acting insulin analog differing from human insulin by replacing 2 amino acids at B3 and B29; produced from E. coli Sterile, clear, aqueous, and colorless solution; stable only in NSS
Insulin Glulisine (Apidra)
167
Sterile aqueous suspension prepared from zinc-insulin crystals with protamine
Isophane Insulin Suspension (NPH Insulin)
168
Long-acting basal insulin preparation intended for SC ODHS administration ■ Recombinant human insulin analog formulated at pH 4.0; formation of microspheres once injected SC
Insulin Glargine
169
Clear neutral solution produced by rDNA in S. cerevisiae ■ Strong self-association and are highly albumin bound ■ Should not be mixed with any other insulin
Insulin Detemir
170
use disposable or single-use cartridges filled with either 150 or 300 U of insulin and packaged five per box. Their ease of use and portability make them desirable for patients to administer insulin, particularly for those patients who desire to avoid the embarrassment of needle use in public
Insulin Pens
171
allow an estimated 300,000 patients to achieve and maintain blood glucose at nearly normal levels on a constant basis through continuous SC insulin infusion.
Insulin Infusion Pumps
172
Infusion of enough basic nutrients to achieve active tissue synthesis and growth ● Characterized by the long-term feeding of protein solutions containing high concentrations of dextrose, electrolytes, vitamins, and in some, insulin. ● Administered slowly through a large vein, permitting rapid dilution and minimizes risk of tissue or cellular damage due to hypertonicity. Dextrose final concentrations of <10% can be given peripherally.
Parenteral Nutrition
173
Orally, via NGT, via feeding gastrostomy, or via needle-catheter jejunostomy. Products contain vitamins, minerals, carbohydrates, proteins, fats, and caloric requirements to meet the specific needs ● Considerations: Type of tubing, Location of the tube, Interactions, Pharmacokinetic concerns
Enteral Nutrition
174
intended to bathe or wash wounds, surgical incisions, or body tissues.
Irrigation
175
Not injected into the vein but employed outside of the circulatory system
Dialysis Solutions
176
solutions are allowed to flow into the peritoneal cavity and remove toxic substances normally excreted by the kidney.
Peritoneal Dialysis
177
is used to remove toxins from the blood
Hemodialysis
178
Pressurized dosage forms upon actuation will deliver a fire mist of the product (liquid/solid drug in a gaseous medium)
AEROSOLS
179
airborne mist
Space spray
180
surface carries active ingredients
Surface spray