Joyce notes Flashcards
Transdermal Systems Should Be Changed every 7 days
a. clonidine patch
b. estradiol patch
c. fentany patch
a. clonidine patch
Transdermal Systems Should Be Changed every once - twice weekly ( depending on brand of production)
a. clonidine patch
b. estradiol patch
c. fentany patch
b. estradiol patch
Transdermal Systems Should Be Changed every 3 days
a. clonidine patch
b. estradiol patch
c. fentanyl patch
c. fentanyl patch
how frequent does lidocaine patch should be changed
a. everyday
b. twice weekly
c. every 3 days
a. everyday( remove for 12 hours each night)
how frequent does nicotine patch should be changed
a. everyday
b. twice weekly
c. every 3 days
a. everyday
how frequent does nitroglycerin patch should be changed
a. everyday
b. twice weekly
c. every 3 days
a. everyday
how frequent does oxybutynin patch should be changed
a. everyday
b. twice weekly
c. every 3 days
b. twice weekly
how frequent does scopolamine patch should be changed
a. everyday
b. twice weekly
c. every 3 days
c. every 3 days
how many mg of epinephrine in 1 mL of a 1:1000 solution?
a. 1
b. 40
c.154
a. 1
how many mEq of potassium in 30 mL of a 10% potassium chloride solution.
a. 1
b. 40
c.154
b. 40
how many % solution of sodium bicarbonate contains 1 mEq each of sodium and bicarbonate ions per
mL?
a. 8.4
b. 154
c. 50
a. 8.4
how many mEq of sodium in 1000 mL of 0.9% sodium chloride?
a. 8.4
b. 154
c. 50
b. 154
how many grams of dextrose in 1000 mL of D5W?
a. 8.4
b. 154
c. 50
c. 50
There are ____ calories in 1000 ml of D50W (500 grams of dextrose).
a. 1700
b. 400,000
c. 0.4
a. 1700
There are ____ units of penicillin in 250 mg.
a. 1700
b. 400,000
c. 0.4
b. 400,000
A nitroglycerin ____ mg sublingual tablet contains 1/150 grains.
a. 1700
b. 400,000
c. 0.4
c. 0.4
vitamin c
a. ascorbic acid
b. cyanocobalamin
c. niacin
d. thiamine
a. ascorbic acid
vitamin B12
a. ascorbic acid
b. cyanocobalamin
c. niacin
d. thiamine
b. cyanocobalamin
nicotinic acid
a. ascorbic acid
b. cyanocobalamin
c. niacin
d. thiamine
c. niacin
vitamin B 1
a. ascorbic acid
b. cyanocobalamin
c. niacin
d. thiamine
d. thiamine
deficiency of this vitamin causes scurvy
a. vitamin C
b. vitamin B 12
c. folic acid
a. vitamin C
deficiency of this vitamin causes pernicious anemia
a. vitamin C
b. vitamin B 12
c. folic acid
b. vitamin B 12 ( cyanocobalamin)
deficiency of this vitamin causes megaloblastic anemia
a. vitamin C
b. vitamin B 12
c. folic acid
c. folic acid
deficiency of this vitamin causes pellegra
a. niacin
b. thiamine
c. vitamin D
a. niacin ( nicotinic acid )
deficiency of this vitamin causes beriberi
a. niacin
b. thiamine
c. vitamin D
b. thiamine (vitamin B1)
deficiency of this vitamin causes wernicke-korsakoff syndrome
a. niacin
b. thiamine
c. vitamin D
b. thaimine (vitamin B1)
deficiency of this vitamin causes rickets
a. niacin
b. thiamine
c. vitamin D
c. vitamin D
match the brand name to its generic name.
vistide
a. cidofovir
b. ganciclovir
c. foscarnet
a. cidofovir
match the brand name to its generic name.
cytovene
a. cidofovir
b. ganciclovir
c. foscarnet
b. ganciclovir
match the brand name to its generic name.
foscavir
a. cidofovir
b. ganciclovir
c. foscarnet
c. foscarnet
match the brand name to its generic name.
vitravene
a. fomivirsen
b. Interferon alfa-2b
c. Lamivudine
a. fomivirsen
match the brand name to its generic name.
Intron A
a. fomivirsen
b. Interferon alfa-2b
c. Lamivudine
b. interferon alfa-2b
match the brand name to its generic name.
Epivir HBV
a. fomivirsen
b. Interferon alfa-2b
c. Lamivudine
c. Lamivudine
match the brand name to its generic name.
zovirax
a. acyclovir
b. famciclovir
c. valacyclovir
a. acyclovir
match the brand name to its generic name.
famvir
a. acyclovir
b. famciclovir
c. valacyclovir
b. famciclovir
match the brand name to its generic name.
valtrex
a. acyclovir
b. famciclovir
c. valacyclovir
c. valacyclovir
match the brand name to its generic name.
symmetrel
a. amantadine
b. rimantadine
c. oseltamivir
d. zanamivir
a. amantadine
match the brand name to its generic name.
Flumadine
a. amantadine
b. rimantadine
c. oseltamivir
d. zanamivir
b. rimantadine
match the brand name to its generic name.
tamiflu
a. amantadine
b. rimantadine
c. oseltamivir
d. zanamivir
c. oseltamivir
match the brand name to its generic name.
Relenza
a. amantadine
b. rimantadine
c. oseltamivir
d. zanamivir
d. zanamivir
match the brand name to its generic name.
rebetron
a. ribavirin
b. rimantadine
c. oseltamivir
d. zanamivir
a. ribavirin
what group of drugs are use to inhibit cytomegalovirus
a. Cidofovir (Vistide)
Ganciclovir (Cytovene)
Foscarnet (Foscavir)
Fomivirsen (Vitravene)
b. Adefovir dipivoxil
Interferon alfa-2b (Intron A)
Lamivudine (Epivir HBV)
a. Cidofovir (Vistide)
Ganciclovir (Cytovene)
Foscarnet (Foscavir)
Fomivirsen (Vitravene)
what group of drugs are use to inhibit hepatitis B virus
a. Cidofovir (Vistide)
Ganciclovir (Cytovene)
Foscarnet (Foscavir)
Fomivirsen (Vitravene)
b. Adefovir dipivoxil
Interferon alfa-2b (Intron A)
Lamivudine (Epivir HBV)
b. Adefovir dipivoxil
Interferon alfa-2b (Intron A)
Lamivudine (Epivir HBV)
what group of drugs are use to inhibit hepatiits C virus
a. Interferon alfa-2b/ribavirin
Pegylated interferon
b. Acyclovir (Zovirax)
Famciclovir (Famvir)
Valacyclovir (Valtrex)
a. Interferon alfa-2b/ribavirin
Pegylated interferon
what group of drugs are use to inhibit herpes simplex virus?
a. Interferon alfa-2b/ribavirin
Pegylated interferon
b. Acyclovir (Zovirax)
Famciclovir (Famvir)
Valacyclovir (Valtrex)
b. Acyclovir (Zovirax)
Famciclovir (Famvir)
Valacyclovir (Valtrex)
what group of drugs are use to inhibit influenza A virus
a. Amantadine (Symmetrel)
Rimantadine (Flumadine)
b. Acyclovir (Zovirax)
Famciclovir (Famvir)
Valacyclovir (Valtrex)
a. Amantadine (Symmetrel)
Rimantadine (Flumadine)
what group of drugs are use to inhibit
Influenza A and B virus
a. Oseltamivir (Tamiflu)
Zanamivir (Relenza)
b. Interferon alfa-2b/ribavirin
Pegylated interferon
a. Oseltamivir (Tamiflu)
Zanamivir (Relenza)
what group of drugs are use to inhibit Respiratory syncytial virus
a. Acyclovir (Zovirax)
Famciclovir (Famvir)
Valacyclovir (Valtrex)
b. Ribavirin (Rebetron)
b. Ribavirin (Rebetron)
what group of drugs are use to inhibit Varicella zoster virus
a. Acyclovir (Zovirax)
Famciclovir (Famvir)
Valacyclovir (Valtrex)
b. Ribavirin (Rebetron)
a. Acyclovir (Zovirax)
Famciclovir (Famvir)
Valacyclovir (Valtrex)
Emulsions made with tweens are usually
A. unstable
B. w/o
C. o/w
D. clear
E. reversible
*(C) Tweens favor o/w emulsions because of high HLB.
Which of the following factors affect the distribution of a drug?
A. Lipid solubility
B. Plasma protein binding
C. Polarity
D. Molecular size
E. All of the above
*(E) All of the factors affect drug distribution.
The rate of zero-order reactions
A. changes constantly
B. is independent of temperature
C. is independent of concentration
D. holds only for light-catalyzed reactions
E. holds only for radioactive compounds
*(C) All other orders are dependent on concentration of one or more substances present.
Spans and tweens are
A. highly polymerized mannuronic acid anhydrides
B. phospholipids
C. polyoxyalkalene derivatives
D. glycosides
E. none of the above
*(C) Spans merely contain fewer oxyethylene groups than tweens.
Lidocaine HCl is not administered orally because it is
A. ineffective by this route
B. too acidic
C. too toxic by this route
D. a cause of arrhythmias
E. unstable
*(A) Oral doses are metabolized by the liver before reaching systemic circulation.
The two major properties of drugs that are usually modified by complexation are
A. odor and taste
B. taste and solubility
C. chemical structure and solubility
D. chemical structure and stability
E. stability and solubility
*(E) Stability and solubility properties may be changed.
What will result if the distribution of drugs is slower than the processes of biotransformation and
elimination?
A. High blood levels of drug
B. Low blood levels of drug
C. Synergism
D. Potentiation
E. Failure to attain diffusion equilibrium
*(E) Drugs will be changed or eliminated before diffusion is attained.
In radiopharmacy, the term rem means
A. radiations per millisecond
B. radiations per minute
C. roentgen-equivalent-man
D. external roentgens per minute
E. roentgen exposure per minute
*(C) The term rem is a measure of exposure to radioactivity.
pH is
A. not temperature dependent
B. a measure of acidity
C. the same as pOH
D. high for acids
E. none of the above
*(B) pH is the negative log of the hydrogen ion concentration (or hydronium ion concentration).
Which of the following types of tissues frequently stores drugs?
A. Fatty tissue
B. Muscle tissue
C. Protein tissue
D. A and B
E. A and C
(E) Muscle tissue is the only one of the three types of tissue that seldom stores drugs.
Which of the following drugs undergoes marked hydrolysis in the GI tract?
A. Aspirin
B. Penicillin G
C. Acetaminophen
D. Hydrocortisone
E. Chlortetracycline
*(B) Hydrolysis of penicillin G is rapid.
Precipitated sulfur is often incorporated into ointments to be used as a
A. parasiticide (e.g., for scabies)
B. emollient
C. keratolytic
D. A and C only
E. A, B, and C
*(D) Ten percent sulfur paste or ointment is used as an alternative treatment for Sarcoptes scabiei.
Sulfur is also used as an active keratolytic. At full strength, it is used alone or in combination with other
keratolytics, such as salicylic acid. If a patient’s skin demonstrates intolerance to sulfur, the concentration
should be reduced.
Solutions that contain bacteriostatic agents
A. cannot be tested for sterility
B. must be cultured on agar plates for sterility tests
C. must be diluted beyond the bacteriostatic level for sterility tests
D. do not require a sterility test
E. are none of the above
*(C) If the solutions are not diluted, a false-negative result is common.
A source of anticarcinogenic drugs is
A. belladonna
B. nux vomica
C. vinca rosea
D. cascara
E. digitalis
*(C) Vinblastine and vincristine are the drugs obtained from vinca rosea.
If a central nervous system (CNS) drug is extensively ionized at the pH of blood, it will
A. penetrate the blood-brain barrier slowly
B. penetrate the blood-brain barrier rapidly
C. not penetrate the blood-brain barrier
D. be eliminated slowly
E. not be distributed to any tissue sites
*(A) The drug must be highly un-ionized to penetrate the blood-brain barrier; this process is quite slow
in general.
Pharmacists should caution patients who are taking niacin that this drug
A. stains the urine bright red
B. causes ringing in the ears
C. causes muscular weakness
D. should be taken before meals
E. should be taken with meals
*(E) Niacin may cause GI upset
If a drug has a biological half-life of 9.6 days, the best dosing interval would be
A. weekly
B. biweekly
C. semiweekly
D. qid
E. daily
*(E) Daily dosing is necessary to maintain therapeutic level. The appropriate dosing interval is
approximately 2.5 times the half-life.
First-order half-life is equal to
A. 1/k
B. k
C. 0.693/k
D. 2k + 1
E. none of the above
*(C) The half-life is equal to 0.693/k in first-order kinetics.
A prescription calls for 25 mEq of potassium chloride. How many grams of KCl (MW 74.6) are
needed?
A. 7.46 g
B. 0.746 g
C. 8.86 g
D. 1.86 g
E. 0.186 g
*(D) 25 × 74.6 ÷ 1000 = 1.86 g.
An IV order requires 5 million units of sodium penicillin G to be added to 100 mL of normal saline.
How many mEq of sodium are present in this solution?
A. 154 mEq
B. 10 mEq
C. 8.4 mEq
D. 25.4 mEq
E. 1620 mEq
*(D) Penicillin G sodium contains 2 mEq of sodium per 1 million units of penicillin G; 100 ml of
normal saline contains 15.4 mEq of sodium (154 mEq/liter).
An order calls for 500 ml of a solution of potassium sulfate to be made so that it contains 10 mEq of
K+. How many grams of potassium sulfate are required?
A. 0.440 g
B. 4.44 g
C. 0.044 g
D. 0.870 g
E. 8.70 g
*(D) 87 g ÷ xg = 1 Eq/500 ml per 0.01 Eq/500 cc; x = 0.87.
How many milliliters of a 10% KCl (MW 74.6) solution contain 5.0 mEq of K+?
A. 2.10 mL
B. 21.0 mL
C. 3.73 mL
D. 37.3 mL
E. 0.373 mL
*(C) 74.6 × 0.05 = 3.73.
One hundred milligrams (100 mg) of a drug are given as an IV bolus. The drug fits a onecompartment, first-order pharmacokinetic model. The volume of distribution is 20 L. The plasma
concentration immediately after administration (at time 0) is
A. 20 mg/L
B. 10 mg/cc
C. 2 mg/cc
D. 5 mg/cc
E. 5 mg/L
*(E) The volume of distribution is the proportionality constant between amount of drug in the body
and plasma concentration. Immediately after administration of a drug by IV bolus, the amount of drug in
the body equals the intravenous dose divided by the volume of distribution. Plasma concentration at time
0 (C0) = IV dose ÷ volume of distribution
Most drugs are
A. strong acids or bases
B. weak acids or bases
C. nonelectrolytes
D. highly ionic
E. none of the above
*(B) Most drugs are weak acids or weak bases.
The major mechanism of degradation of drugs in the GI tract is
A. oxidation
B. hydrolysis
C. acetylation
D. conjugation
E. reduction
*(B) Hydrolysis occurs to some degree with many drugs.
Sodium bicarbonate is compatible with which of the following IV medications?
A. Potassium chloride
B. Calcium salts
C. Atropine
D. Catecholamines
E. All of the above
*(A) Due to its high pH, sodium bicarbonate is incompatible with many common IV medications.
The pKw of water at 25°C is
A. 7
B. 14
C. 1 × 10–14
D. 1 × 10–7
E. 1
*(B) This ion product is obtained by adding the pH and pOH.
Which of the following is not a major pathway or type of biotransformation?
A. Oxidation
B. Deamination
C. Reduction
D. Hydrolysis
E. Conjugation
*(A) Oxidation pathways are less common in vivo
When making pharmacokinetic recommendations in aminoglycoside dosing, if you want to
decrease only the trough concentration, you would
A. decrease the dose
B. take the trough measurement 3 hours before the next dose
C. lengthen the dosing interval
D. increase the dose
E. none of the above
*(C) Trough concentrations are indicative of drug accumulation. To decrease only the trough level and
maintain peak concentrations, lengthening the dosing interval is the method of choice.
The dose of a drug is 0.5 mg/kg. What dose should be given a 6-year-old child who weighs 44 lb?
A. 0.003 g
B. 0.033 g
C. 0.010 g
D. 0.100 g
E. 0.05 g
*(C) 0.5 mg ÷ x mg = 2.2 lb/44 lb; x = (10) mg (0.01 g). (Age not relevant).
If a prescription order requires 30 gs of concentrated sulfuric acid (density is 1.8 g/mL), what
volume should the pharmacist measure?
A. 1.67 mL
B. 18 mL
C. 30 mL
D. 16.67 mL
E. 166.7 mL
(D) Volume = weight ÷ density. Thus, volume = 30 g ÷ 1.8 g/mL = 16.67 mL.
Calculate the weight of 25 mL of hydrochloric acid whose density is 1.18 g/mL.
A. 29.5 g
B. 2.95 g
C. 0.295 g
D. 295 g
E. None of the above
*(A) Weight = density × volume. Thus, weight = 1.18 g/mL × 25 mL = 29.5 grams
In most biotransformation reactions, the metabolite of a drug
A. is more polar than the parent compound
B. is more lipid-soluble than the parent compound
C. has a longer t1/2 than the parent compound
D. is all of the above
E. is none of the above
*(A) For most drugs, biotransformation results in conversion to a more polar compound, which is more
easily cleared by the kidney.
To calculate a loading dose, one must first determine
A. t1/2
B. body clearance
C. fraction protein bound
D. volume of distribution
E. all of the above
*(D) The optimal loading dose is easily estimated by use of the following formula:
Loading dose = desired plasma concentration × volume of distribution
Convert 60 grams to grains
A. 9240 grains
B. 924 grains
C. 9.24 grains
D. 0.924 grains
E. 0.0924 grains
*(B) 15.4 grains = 1 gram. Thus, 60 grams × 15.4 grains/gram = 924 grains.
Radioactive decay follows a
A. mixed-order rate
B. fractional-order rate
C. zero-order rate
D. first-order rate
E. second-order rate
*(D) It is a classic type of first-order reaction.
The HLB system is used to classify
A. flavors
B. colors
C. surfactants
D. organic ring structures
E. perfumes
*(C) It is a measure of oil and water balance in emulsions.
Alpha particles are very similar to
A. hydrogen atoms
B. helium atoms
C. neutrons
D. protons
E. electrons
*(B) Alpha particles and helium atoms have the same mass.
To achieve the same steady-state plasma concentration (for a drug that is excreted by the kidney) in
renal failure patients as in patients with normal renal function, you should
A. increase the dosing interval
B. decrease the dose
C. adjust both the dose and the dosing interval
D. do any of the above, depending on the pharmacodynamic properties of the drug
E. not adjust the dosing regimen unless the patient shows signs of toxicity
*(D) Both adjustment of dosage interval and dosage size reduction are acceptable methods for
decreasing drug accumulation in patients with renal failure. The two methods may be used in
combination, depending on the dosage forms available, the therapeutic range, and convenience.
The most common disintegrator in compressed tablets is
A. dextrose
B. lactose
C. starch
D. potassium bitartrate
E. powdered sucrose
*(C) Corn or potato starch is used.
Freons are
A. alkanes
B. alkenes
C. alkynes
D. fluorinated hydrocarbons
E. a mixture of CO2 and air
(D) These fluorinated hydrocarbons are used as propellants in aerosols.
Which of the following factors may make it necessary to give lower doses of drugs to geriatric
patients?
A. Reduced enzyme activity
B. Reduced kidney function
C. Enhanced absorption
D. A and B only
E. A, B, and C
*(D) The liver and kidneys commonly become less functional in the elderly.
Convert 2 pints 3 fluid ounces into mL.
A. 1500 mL
B. 1050 mL
C. 150 mL
D. 105 mL
E. 10.5 mL
*(B) Assume 16 oz/pint, and 30 mL/oz. Thus,
2 pt × 16 oz/pt = 32 oz
(32 oz × 30 mL/oz) + (3 oz × 30 mL/oz) = 960 mL + 90 mL
= 1050 mL
Tablet hardness range is normally
A. 0.2 to 0.5 kg
B. 0.5 to 1.0 kg
C. 1.0 to 2.0 kg
D. 2.0 to 3.5 kg
E. 3.5 to 7.0 kg
*(E) Less than 3.5 kg hardness tablets would cause fragmentation during shipping.
An antidote for heparin overdosage is
A. protamine sulfate
B. BAL
C. atropine
D. calcium salts
E. dicumarol
*(A) Protamine sulfate is the primary antidote.
Which of the following may be used as plasma expanders?
A. Sodium salts
B. Dextrans
C. Mannitol
D. Calcium salts
E. Prostaglandins
(B) Dextrans are inert and soluble, so they cause no problems.
The dose of a drug is 0.6 mg. How many doses are contained in 96 mg of the drug?
A. 16
B. 160
C. 360
D. 600
E. None of the above
(B) 96 mg ÷ 0.6 mg/dose =160 doses
The expression ppm as used in compounding prescriptions most often is defined as
A. parts per million
B. parts per mL
C. parts per mole
D. pieces per million
E. parts per molar
*(A) The term ppm is typically used in expressing concentrations of very dilute preparations and is
defined as “parts per million.”
GMP regulations (USFDA) primarily apply to
A. controlled drugs
B. wholesalers
C. pharmaceutical manufacturers
D. hospital pharmacy
E. community pharmacy
*(C) These are good manufacturing practices.
pH is equivalent to pka at
A. pH of 7
B. pH of 1
C. pH of 14
D. half neutralization point
E. neutralization point
*(D) At this point acid/base is 1.0 and log of 1 is 0; so pH = pka.
Popular theory of acids and bases is
A. Boyle’s law
B. Four Humors’ theory
C. Pythagorean theory
D. Brønsted-Lowry theory
E. Henry’s theory
*(D) The Brønsted-Lowry theory is the proton donor-acceptor theory of acids and bases.
Salicylic acid is used primarily as a(n)
A. analgesic
B. antipyretic
C. cough suppressant
D. uricosuric agent
E. keratolytic agent
*(E) Salicylic acid is used in topicals to cause sloughing of skin
In dosing aminoglycosides, which of the following patient populations commonly require an
extended interval (>8 hours)?
A. Elderly patients
B. Neonatal patients
C. Cystic fibrosis patients
D. A and B
E. All of the above
*(D) Cystic fibrosis patients commonly clear aminoglycosides very quickly and may even require
dosing intervals of every 6 hours.
Glycerin has a specific gravity of 1.25. One gallon weighs
A. 591.25 g
B. 473 g
C. 4528.0 g
D. 128 g
E. 4800 g
*(C) A specific gravity of 1.25 means that 1 fluid ounce (volume) weighs 1.25 ounces (weight). In
avoirdupois measurement, 1 ounce = 28.3 grams. There are 128 ounces in 1 gallon.
Vitamin K is associated with
A. pellagra
B. nerves
C. hemoglobin concentration
D. bones
E. blood clotting
*(E) Vitamin K is necessary for formation of prothrombin.
Another name for polyethylene glycol polymers is
A. sodium alginate
B. silica gel
C. carbowax
D. Friar paste
E. none of the above
*(C) Carbowax is merely a trade name used for this group.
Which of the following is found in vitamin B12?
A. Magnesium
B. Nickel
C. Iron
D. Cobalt
E. Manganese
*(D) Cobalt is an element in the chemical structure of cyanocobalamin (Vitamin B12).
–12°C is equivalent to
A. 36°F
B. 12°F
C. 10.4°F
D. 5°F
E. –2°F
*(C) °F = 9/5 (–12°C) + 32 = 10.4°F
One tablespoon is approximately equivalent to
A. 15 mL
B. 10 mL
C. 8 mL
D. 20 mL
E. 30 mL
*(A) One tablespoon is about one-half ounce, or 15 mL.
When describing solubility terms, >10,000 parts of solvent for 1 part of solute would be called
A. very soluble
B. soluble
C. sparingly soluble
D. slightly soluble
E. practically insoluble or insoluble
*(E) More than 10,000 parts of solvent per one part of solute is considered practically insoluble or
insoluble.
The amount of 190 proof required to make 500 mL of 70% alcohol is
A. 350 mL
B. 250 mL
C. 184 mL
D. 368 mL
E. 37 mL
*(D) 190 proof is 95% alcohol. 70 ÷ 95 = x ÷ 500; x = 368 mL
Which of the following dose forms is specifically covered by the Federal Hazardous Substance
Labeling Act?
A. Parenterals
B. Aerosols
C. Tinctures
D. Ophthalmic solutions
E. Nitroglycerin tablets
*(B) Dose forms of aerosols are covered by the Federal Hazardous Substance Labeling Act because
they are in pressurized containers, which could explode.
The chemical substance used commonly in running a GI series is
A. barium sulfate
B. fluorescein dye
C. radioactive iodine
D. sodium bicarbonate
E. sodium carbonate
*(A) Barium sulfate creates an opaque medium for x-ray.
Which of the following ions plays a significant role in preventing convulsions?
A. Potassium
B. Lithium
C. Magnesium
D. Phosphorus
E. Fluoride
*(C) Magnesium controls convulsions by locking neuromuscular response
Colleges of pharmacy are accredited by
A. the AFPE
B. the AACP
C. the ACPE
D. the NABP
E. none of the above
*(C) The American Council on Pharmaceutical Education accredits all schools.
Denaturation of emulsions is characterized by
A. irreversible precipitation
B. reversible precipitation
C. creaming
D. changing of external phase
E. C and D
*(A) If creaming or reversible precipitation occurs, the emulsion can be reestablished. Change of phase
does not always result in precipitation.
Freeze drying is based on
A. pressure filtration
B. sublimation
C. polymerization
D. pasteurization
E. densification
*(B) In this process, water is sublimed from a frozen product. The other answers represent different
processes.
Characteristics of pyrogens include the following.
I. They usually cause a febrile reaction in humans
II. They may cause pains in the back and legs
III. They may cause chills
A. I only
B. III only
C. I and II only
D. I and III only
E. I, II, and III
*(E) Pyrogens can commonly cause all of the symptoms listed.
Lubricants in tablets serve the following functions.
I. They improve the flow of tablet granulation
II. They prevent adhesion to dies and punches
III. They facilitate ejection from die cavity
A. I only
B. II only
C. I and II only
D. I and III only
E. I, II, and III
*(E) Lubricants such as talc or stearates facilitate all three functions.
The most prevalent commercial solid dosage forms are
A. hard capsules
B. soft gelatin capsules
C. tablets
D. bulk powders
E. divided powders
*(C) Tablets comprise about 75% of all solid dosage forms, followed by hard capsules (23%), and soft
elastic capsules (2%)
Which of the following is not a naturally occurring emulsifier?
A. Acacia
B. Cholesterol
C. Gelatin
D. Veegum
E. Tragacanth
*(D) Veegum is a synthetic hydrophilic thickening agent.
The purpose of sorbitol in formulations of soft gelatin capsules is as a(n)
A. plasticizer
B. disintegrating agent
C. lubricant
D. thickener
E. emulsifier
*(A) Sorbitol renders the shells elastic. It can also be used as a thickener or emulsifier, but only in
liquid dose forms.
Hard gelatin capsules for human use are available in the following sizes.
I. 1
II. 00
III. 0000
A. I only
B. II only
C. III only
D. I and II only
E. I, II, and III
*(D) Capsules for human use are available in sizes from 000 (largest) to 5 (smallest). Size 0000 would
be too large to swallow.
Ointments are typically used as
I. emollients
II. protective barriers
III. vehicles for applying drugs
A. I only
B. III only
C. I and II only
D. II and III only
E. I, II, and III
*(E) The three applications listed are the main uses of ointment: to soften, to protect, and to serve as a
semisolid carrier.
A humectant retards
A. bacterial growth
B. degradation
C. surface evaporation
D. spreadability
E. all of the above
*(C) A humectant such as glycerin helps to retain moisture and prevent drying due to evaporation
The Noyes-Whitney equation describes
A. zero-order kinetics
B. first-order kinetics
C. mixed-order kinetics
D. dissolution rate
E. renal clearance
*(D) The Noyes-Whitney equation is used to determine dissolution rate and does not describe any
other biopharmaceutical functions.
Which of the following properties are characteristic of flocculated particles in suspension?
A. Particles form loose aggregates
B. Rate of sedimentation is high
C. A sediment is formed rapidly
D. The sediment is loosely packed
E. All of the above
*(E) All of the above are characteristics of flocculated particles in a suspension. The rate of
sedimentation is high, because particles settle as a floc (a collection of particles). Although a sediment is
formed rapidly, it is loosely packed and possesses a scaffold-like structure. Because the particles do not
bond tightly, caking does not occur. The suspension may not appear uniform due to rapid sedimentation.
Starch is used in tabletting as a
I. binder
II. glidant
III. disintegrant
A. II only
B. III only
C. I and II only
D. II and III only
E. I, II, and III
*(E) Starch in the form of a paste can serve as a binder. It also exhibits glidant properties and can help
with disintegration when it comes in contact with body fluids.
Gums are used in tabletting primarily as
A. disintegrators
B. glidants
C. lubricants
D. binding agents
E. both B and C
Gums are effective only as binders. They increase hardness and tend to impede lubrication or
flow.
Which of the following is (are) true for buccal and sublingual tablets?
I. They are useful for drugs destroyed by gastric fluid
II. They are readily soluble
III. They are useful for drugs that are poorly absorbed in the intestinal tract
A. I and II only
B. II and III only
C. II only
D. III only
E. I, II, and III
*(E) All three statements are true because these tablets must dissolve in the mouth readily and they
bypass GI tract absorption.
Syrup NF is
A. self-preserving
B. a supersaturated solution
C. a dilute solution
D. highly unstable
E. flavored and preserved
*(A) Although syrup NF has a high enough concentration of sucrose to retard bacterial growth, it is not
a saturated solution. This ensures good stability.