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Foreign

Pharmacy
Graduate
Equivalency
Examination®
(FPGEE®)

Study Guide
FPGEE Study Guide

©2007 by the National Association of Boards of Pharmacy. All rights reserved.

No part of this publication may be reproduced in any manner without the written permission of the Executive
Director/Secretary of the National Association of Boards of Pharmacy. Violation of the copyright will lead to
prosecution under federal copyright laws.

National Association of Boards of Pharmacy reg. no. 1,162,334


NABP reg. no. 1,160,482
Foreign Pharmacy Graduate Equivalency Examination reg. no. 2,270,607
FPGEC reg. no. 2,113,836
FPGEE reg. no. 2,337,295

National Association of Boards of Pharmacy


Foreign Pharmacy Graduate Examination Committee
1600 Feehanville Drive
Mount Prospect, IL 60056
USA
847/391-4406
www.nabp.net

Carmen A. Catizone, MS, RPh, DPh


Executive Director/Secretary
1/07
Table of
Contents
FPGEE Blueprint ................................................................................... 1
Sample Questions ................................................................................... 7
Answer Key........................................................................................... 13
Textbooks Commonly Used in US Pharmacy Schools ...................... 15
FPGEE Blueprint

FPGEE Administration 2. Pathophysiology of disease states


The Foreign Pharmacy Graduate Equivalency amenable to pharmacist intervention
Examination® (FPGEE®) is based on a nationally C. Microbiology
uniform content blueprint. The following blueprint, 1. General principles of microbial concepts
revised in 2007, provides important information 2. Principles of infectious disease
about the topics covered on the examination and the 3. Host-parasite relationships
knowledge you are expected to demonstrate while
4. Pathogenic micro-organisms of man
taking the FPGEE.
The examination is a comprehensive measure of 5. Inflammatory responses to infectious
knowledge in four major pharmacy content areas: agents
21% – Basic Biomedical Sciences 6. Clinical aspects of infection
29% – Pharmaceutical Sciences D. Immunology
15% – Social/Behavioral/Administrative 1. Human immunity and immune responses
Pharmacy Sciences 2. Principles of antigen-antibody
35% – Clinical Sciences relationships
You must take the examination at one of two 3. Molecular biology of immune responses
consecutive opportunities upon being qualified to 4. Genetic basis for antibody synthesis,
take the FPGEE. One additional opportunity to take development, function and
the FPGEE will only be allowed if NABP receives immunopathology
an official denial of your visa request or health E. Biochemistry/Biotechnology
documentation from a health care provider stating that
1. Chemistry of biomacromolecules
you can not attend your second opportunity.
(proteins, lipids, carbohydrates, and
A strong understanding of the following DNA)
blueprint will aid in your preparation to take the
2. Enzymology and co-enzymes and
examination.
kinetics
Area 1 – Basic Biomedical Sciences – 21% 3. Metabolic pathways to energy utilization
A. Anatomy & Physiology 4. Nucleic acid metabolism including DNA
1. Structure and function of major body replication and repair, RNA and protein

FPGEE Blueprint
systems; integumentary, muscular synthesis
skeletal, cardiovascular, lymphatic, 5. Recombinant DNA technology
respiratory, digestive, nervous, endocrine, F. Molecular Biology/Genetics
urinary, reproductive and body fluid and 1. Cell structure and components
electrolytes
2. Ion channels and receptor physiology
2. Molecular aspects of cell biology
3. Mitosis and meiosis
3. Cell physiology and cellular structure and
4. Chromosomes and DNA
organization
5. Gene transcription and translation
B. Pathology/Pathophysiology
processes
1. Basic principles and mechanisms of
6. Recombinant DNA technology
disease including:
G. Biostatistics
a. Inflammation and repair
1. Understanding commonly used statistical
b. Degeneration
tests and their basis
c. Disturbances and hemodynamics
2. Management of data sets
d. Developmental defects
3. Evaluation of statistical results
e. Neoplasia

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4. Understanding of statistical versus clinical 5. Functions of poison control centers
significance 6. Bioterrorism and disaster preparedness and
Area 2 – Pharmaceutical Sciences – 29% management
A. Medicinal Chemistry E. Bioanalysis/Clinical Chemistry
1. Physio-chemical properties of drug molecules 1. Fundamentals of laboratory medicine and
in relation to drug absorption, distribution, its importance to screening, diagnosis, and
metabolism, and excretion (ADME) evaluation of patients
2. Chemical basis and pharmacology and 2. Clinical data relevant to disease state
therapeutics management
3. Fundamental pharmacophores for drugs used F. Pharmaceutics/Biopharmaceutics
to treat disease 1. Physical-chemical principles of dosage forms
4. Structure activity relationships in relation to 2. Biological principles of dosage forms
drug-target interactions 3. Principles of drug delivery via dosage forms
5. Chemical pathways of drug metabolism (eg, liquid, solid, semi-solid, controlled
6. Application to making drug therapy decisions release, patches, and implants)
B. Pharmacology 4. Principles of dosage form stability and drug
1. Mechanism of action of drugs of various degradation in dosage forms
categories 5. Materials and methods used in preparation
2. Role of pharmacology in drug choice and the and use of drug forms
treatment of disease G. Pharmacokinetics/Clinical Pharmacokinetics
3. Pharmacodynamics of drug action and 1. Basic principles of in vivo drug kinetics
absorption, distribution, metabolism, and (linear and nonlinear)
elimination 2. Principles of bioavailability/bioequivalence
4. Adverse effects and side-effects of drugs 3. Physiologic determinates of drug onset and
5. Drug-target interactions duration
6. Drug-drug, drug-food, drug-lab test interactions 4. Drug, disease, and dietary influences on
7. Drug discovery and development absorption, distribution, metabolism, and
C. Pharmacognosy and Alternative and excretion
Complementary Treatments 5. Clinical pharmacokinetics of commonly used
1. Concepts of crude drugs, semi-purified, and and low-therapeutic-index drugs
purified natural products 6. The pharmacokinetic-pharmacodynamic
2. Variability of occurrence of interface
pharmacologically active substances in plants H. Pharmacogenomics/Genetics
and impact on regulatory aspects of herbal 1. Genetic basis for disease and drug action
products 2. Genetic basis for alteration and drug
3. Overview of classes of pharmacologically metabolism
active natural products 3. Genome and proteomic principles in relation
4. Dietary supplements (vitamins, minerals, and to disease and drug development
herbals) 4. Genetic basis for individualizing drug doses
5. Alternative medical treatments I. Extemporaneous Compounding/Parenteral/Enteral
6. Evaluation of alternative and complementary 1. United States Pharmacopeia (USP) guidance
medicine purity, bioavailability, safety, and on compounding and Food and Drug
efficacy Administration (FDA) Compliance Policy
7. Herbal-drug interactions Guidelines
8. Dietary Health Supplement and Education 2. Techniques and principles used to prepare
Act and impact on regulation of dietary and dispense individual extemporaneous
supplements and herbal products prescriptions including dating of compounded
D. Toxicology dosage forms
1. Mechanism of toxicity and toxicokinetics 3. Liquid (parenteral, enteral), solid, semi-solid,
2. Acute and chronic toxic effect of xenobiotics and topical preparations
on the body including drug or chemical 4. Dosage form preparation calculations
overdose and toxic signs of drugs of abuse 5. Sterile admixture techniques
3. Interpretation of drug screens a. USP Chapter 797
4. Antidotes and approaches to toxic exposures b. Stability and sterility testing and dating

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c. Clean room requirements 10. Project management
d. Infusion devices and catheters 11. Managing and improving the medication-
Area 3 – Social/Behavioral/Administrative use process
Pharmacy Sciences – 15% 12. Third-party administration and managed
A. Health Care Delivery Systems care systems
1. Introduction to United States, state, and 13. Health care improvement mechanisms at
local health care delivery systems and the micro- and macro-system levels
their interfaces D. Pharmacoepidemiology
2. Social, political, and economic factors of 1. Application of principles of
the US health care delivery system epidemiology to the study of drug use
3. Principles that influence the distribution and outcomes in large populations
of pharmaceutical products and services 2. Studies that provide an estimate of
4. Role of public and private insurers, the probability of beneficial effects
pharmaceutical industry, and managed in populations, or the probability of
care on health care delivery in the United adverse effects in populations, and other
States parameters relating to drug use may
5. Medicare and Medicaid benefit
6. Indigent care programs 3. Methods for continual monitoring for
7. Incidence of and problems associated unwanted effects and other safety-related
with drug overuse, underuse, and misuse aspects of drugs
in the US health care system E. Pharmacy Law and Regulatory Affairs
B. Economics/Pharmacoeconomics 1. Legal basis for pharmacy practice
1. Economic principles in relation to 2. Pharmacist’s responsibilities and limits
pharmacoeconomic analysis under the law
2. Concepts of pharmacoeconomics in 3. Pharmacist’s role in reducing liability by
relation to patient care reducing drug-related misadventure
3. Applications of economic theories and 4. Civil versus criminal liability
health-related quality-of-life concepts to 5. Business contract law
improve allocation of limited health care F. History of Pharmacy
resources 1. Overview of the evolution of pharmacy
C. Practice Management as a distinct profession
1. Management principles (planning, 2. Moving from focus on the drug to focus
organizing, directing, and controlling on the patient and the drug, including
pharmacy resources) applied to various clinical, pharmaceutical care and other
pharmacy practice setting and patient aspects of patient-provided pharmacist
outcomes care
2. Management of staff within the 3. Major milestones and contributors in the
practice setting including pharmacists, evolution of pharmacy
technicians, and other supportive G. Ethics
personnel

FPGEE Blueprint
1. Principles of professional behavior
3. Principles of planning, organizing, 2. Ethical issues related to the development,
directing, and controlling pharmacy promotion, sales, prescription, and use of
resources drugs
4. Tools, including informatics, needed 3. Dealing with ethical dilemmas
to assess and address change, increase 4. Conflict of interest
competitiveness, improve quality, and
5. Ethical issues in delivery of patient-
optimize patient services
centered care and clinical research
5. Management of medication use safety
6. Principles of end-of-life care
systems
7. Ethical issues in teamwork
6. Strategies to improve continuity of
patient care as patients move between H. Professional Communications
health care settings 1. Effective verbal and written interpersonal
7. Marketing principles communication
8. Basic accounting principles 2. Health literacy
9. Infection control 3. Communicating with diverse patients,
families, pharmacists, and other health

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professionals in a variety of settings both 6. Role of automation and technology in
individually and as a member of a team workload efficiency and patient safety
4. Interviewing techniques 7. Assurance of safety in the medication-use
5. Active listening and empathy process
6. Assertiveness and problem-solving 8. Medication error reduction programs
techniques 9. Continuous quality improvement programs
7. Cultural influences on communication of C. Pharmacotherapy – Practice Guidelines and
health information Clinical Trials
8. Group presentation skills 1. Principles of clinical practice guidelines for
9. Strategies for handling difficult situations various disease states and their interpretation
10. Documentation of pharmacist in the clinical setting
recommendations and consultations 2. Integration of core scientific and systems-
11. Principles of behavior modification based knowledge in patient care decisions
I. Social and Behavioral Aspects of Practice 3. Reinforcement of basic science principles
1. Pharmacy as a patient-centered profession relative to drug treatment protocols and
clinical practice guidelines
2. Patient and other health care providers
perceptions of pharmacists’ capabilities 4. Evaluation of clinical trials that validate
treatment usefulness
3. Role of pharmacist related to patient care
D. Pharmacotherapy – Health Promotion/Disease
4. Role of pharmacist related to interaction with
Prevention
other health care professionals
1. Promotion of wellness and nonpharmacologic
5. Development of leadership skills
therapies
6. Importance of involvement in pharmacy
2. Disease prevention and monitoring
organizational, regulatory, state, and federal
issues E. Pharmacotherapy – Pharmaceutical Care
Area 4 – Clinical Sciences – 35% 1. Application of evidence-based decision
making to patient care
A. Pharmacy Practice and Pharmacist-Provided Care
2. Drug monitoring for positive and negative
1. Overview of the pharmacy profession
outcomes
2. Issues of contemporary practice
3. Diagnostic tests in the diagnosis, staging, and
3. Emerging and unique roles for the pharmacist monitoring of various disease states
on the health care team
4. Concepts of pain management and palliative
4. Concepts of pharmacist-provided patient care care
and medication therapy management services
5. Nonprescription drug therapies
5. Principles of pharmacist-managed, patient-
6. Dietary drug therapies
centered pharmacy services
7. Designing of patient-centered, culturally
6. Methods of outcome monitoring and
relevant treatment plans
assessment techniques
8. Drug-induced disease
7. Problem identification (eg, duplication,
dosage, drug interactions, adverse drug F. Pharmacist-provided Care for Special Populations
reactions and interactions, frequency, dosage 1. Pathophysiologic and pharmacotherapy
form, indication mismatches) and resolution alterations specific for special population
8. Role of pharmacy care plans in patient care patients (eg, pediatric, geriatric, pregnant,
cystic fibrosis, sickle cell anemia, celiac
9. Monitoring for positive and negative drug
disease, genetic disorders, and others) for
therapy outcomes
prescription and nonprescription medications
10. Principles of clinical management of drug
2. Dosage calculation and adjustment in special-
toxicity and overdosage
population patients
11. Home diagnostic devices
3. Drug monitoring for positive/negative
B. Medication Dispensing and Distribution Systems outcomes in special-population patients
1. Preparation and dispensing of prescriptions G. Drug Information
2. Development and maintenance of patient 1. Fundamentals of the practice of drug information
medication profiles
2. Application of drug information skills for
3. Identification and prevention of medication delivery of pharmaceutical care
errors
3. Technology of drug information retrieval for
4. Identification and prevention of drug toxicity quality assurance
5. Issues of distribution systems associated with
all types of practice settings

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4. The ability to judge the reliability of 2. Familiarity with basic assessment
various sources of information techniques (inspection, palpation,
H. Medication Safety percussion, auscultation), terminology,
1. Causes of medication errors/systems and the modifications caused by common
approaches disease states and drug therapy
2. Human factors in errors 3. Triage and referral skills
3. Strategies for reducing errors 4. Knowledge of therapeutic drug
concentrations and their interpretation
4. Pharmacy leadership in medication safety
5. Knowledge of the basis for common
I. Literature Evaluation and Research Design
clinical laboratory values and diagnostic
1. Fundamentals of research design and tests and the influences of common
methodology disease states
2. Principles of evaluation of the primary 6. False positive and false negative results
literature
7. Over-the-counter point-of-care testing
3. Practical implications of the primary devices (eg, glucometers, pregnancy
literature tests, home testing for HbA1c, drug
4. Principles of research design and analysis screening)
in practicing evidence-based pharmacy 8. Principles of electrocardiography and
J. Patient Assessment Laboratory common EKG abnormalities
1. Obtaining a comprehensive patient 9. Advanced cardiac life support
history

FPGEE Blueprint

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6
Sample Questions

Sample Questions 4. Viruses, bacteria, and parasites evade the


The following questions are typical of those immune system by many different
found on the FPGEE. However, their overall mechanisms. When parasites and viruses
difficulty is not necessarily representative of the acquire a coating of host antigens, it is
overall difficulty of the actual examination, nor do called:
they provide a complete overview of the content of
the entire 300-item examination. The questions are A. antigen masking.
organized by the four major content areas of the B. antigenic variation.
examination. Figures in parentheses indicate the C. overwhelming the immune system.
percentage of items that are covered by that area. D. hiding inside cells.
For example, 21% of the 300 items on the
examination relate to Area I, Basic Biomedical
Sciences. An answer key is provided on page 13.
5. What is the formula for the Keq of the
reaction shown below?
Area 1 – Basic Biomedical Sciences – 21%
2A + B C + 2D
1. Strand breaking in DNA is primarily due
to:

A. deamination.
B. loss of a purine and pyrimidine base. [C][D]2
C. hydrolysis of a phosphodiester bond.
D. hydrolysis of the N-glycosidic bond. A. [A]2[B]

2. What hormone is primarily responsible for


the maintenance of a normal plasma [C] + [D] 2
calcium level in mammals?

Sample Questions
B. [A] 2 + [B]
A. Glucagon
B. Thyroxine
C. Calcitonin
D. Parathyroid hormone [C][D] x 2

C. [A] x 2 x [B]
3. Inflammation from Propionibacterium
acnes is due in part to the:

A. production of fatty acids. [A]2[B]


B. hydrolysis of disaccharides.
C. bacterial release of histamine. D. [C][D]2
D. release of purines from DNA
degradation.

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6. Which of the following carbohydrates is a 8. Which of the following arrangements lists
disaccharide? the compounds below in the order of
decreasing acidity (most acidic first, least
A. Dextrose acidic last)?
B. Mannose
C. Galactose H
D. Maltose
Cl C COOH

7. Lidocaine has a longer duration of action 1. H


than procainamide because it:
H
CH3 CH3
O
H C OH
N CH3
N
H
2. H
CH3

Lidocaine OH

H 2N
H
N
N CH3
O
CH3
3.

Procainamide
Cl

A. lacks a nucleophilic aniline. Cl C COOH


B. contains a non-hydrolyzable amide.
C. has more hydrophobic character. 4. Cl
D. is protected from hydrolysis by ortho
methyl groups.

A. 1>2>3>4
B. 1>4>3>2
C. 3>4>1>2
D. 4>1>3>2

Area 2 – Pharmaceutical Sciences – 29%

9. Rifampin can be responsible for drug-drug


interactions because it:

A. inhibits human RNA polymerase.


B. stimulates human RNA polymerase.
C. inhibits hepatic microsomal enzymes.
D. induces hepatic microsomal enzymes.

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10. Nystatin functions as an antifungal by: 15. Which of the following statements best
defines adsorption?
A. inhibiting mitosis.
B. inhibiting CYP 450 enzymes. A. Diffusion of one compound through
C. interrupting cellular processes. the bulk phase of another compound
D. selective disruption of the membrane. B. Penetration of a compound from
higher concentration to lower
concentration
11. The drug which binds to gastric and C. Accumulation of a compound at an
pancreatic lipases, inhibits their activity, interface
and prevents absorption of dietary fat is: D. Penetration of a compound from
lower concentration to higher
A. miglitol. concentration
B. sibutramine.
C. acarbose.
D. orlistat. 16. The cholesterol in an absorption ointment
base with added water acts as:

12. An antibiotic's volume of distribution is A. a water-in-oil emulsifier.


12 L, and its elimination rate constant is B. a micellar solubilizer.
0.25/h.
C. an agent to increase viscosity.
To maintain a steady state plasma D. an agent to increase surface tension.
concentration of 10 mcg/mL, what should
the infusion rate be?
17. A preservative with a weight to volume
A. 20 mcg/h ratio of 1:8000 is present in a vaccine that
B. 40 mcg/h is to be dosed at 0.05 mL/kg of body
C. 10 mg/h weight. How many micrograms of
D. 30 mg/h preservative is contained in a dose
prepared for a 15-kg child?
13. The expiration period for a reconstituted A. 6.2
product is 20 hours at room temperature B. 43
(25°C). What is the approximate
C. 94
expiration period for the same product D. 400
stored in a refrigerator (5°C)?

A. 25 hours 18. Patients beginning ciprofloxacin should


B. 80 hours be counseled that the drug:
C. 300 hours
D. 450 hours A. should be taken with food.

Sample Questions
B. should not be taken with antacids.
C. may discolor the urine.
14. Polysorbate 20 and polysorbate 80 are D. may darken the stools.
present in intravenous multivitamin
preparations containing vitamins A and D.
The polysorbates function as:

A. stabilizers.
B. solubilizing agents.
C. viscosity enhancers.
D. ionic strength adjusters.

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19. The primary advantage of using insulin 22. A preparation for a Schedule III substance
lispro over other biotech-produced is written March 15 and dispensed April
insulins is: 30. Authorized refills are not permitted
after:
A. a more rapid onset.
B. fewer immune reactions. A. June 14.
C. a lack of pyrogens. B. June 29.
D. a more prolonged action. C. September 14.
D. September 29.

20. The half-life of theophylline (shown in the


structure below) is reduced in smokers 23. Which of the following groups may
due to induction of the metabolizing prescribe legend drug products?
enzyme:
A. Dentists
B. Chiropractors
O
C. Physical therapists
H D. Registered dietitians
H 3C N
N

O N N
24. Community-based pharmacists spend the
CH 3
largest percentage of their time:

Theophylline A. dispensing prescriptions.


B. counseling patients.
C. consulting with physicians.
A. COX-1. D. supervising technicians.
B. CYP1A2.
C. phosphodiesterase.
D. monoamine oxidase. 25. Persons who are becoming socialized into
a profession are most likely to change
their:
Area 3 – Social/Behavioral/Administrative
Pharmacy Sciences – 15%
A. personality traits.
21. The largest segment of total health-care B. attitudes.
expenditures is for: C. religious values.
D. parental relationships.

A. medications.
B. hospital care. 26. The age group that has the highest
C. nursing home care. documented incidence of improper use of
D. physician services. medication is composed of individuals:

A. 65 years of age and older.


B. between 30 and 50 years old.
C. between 12 and 21 years old.
D. under 12 years old.

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Area 4 – Clinical Sciences – 35% 31. When adding spironolactone to a
treatment regimen containing furosemide
27. A news report states that the prevalence of and lisinopril, it is most important to
type 2 diabetes is 6.6%. What does the monitor for:
6.6% represent?
A. hirsutism.
A. The sensitivity of diabetes screening B. hypotension.
at a point in time C. hyperkalemia.
B. The accuracy of diabetes screening D. acute renal failure.
over a time period
C. Diabetes patients present in the
population at a point in time 32. A patient with flushed red face, dilated
D. New diabetes patients diagnosed in pupils, hot and dry skin, sinus tachycardia,
the population over a time period ileus, hallucinations, and combative
behavior is most likely to have been
poisoned by:
28. Which of the following findings is not
compatible with acute salicylate toxicity A. a narcotic analgesic.
in a child? B. a benzodiazepine.
C. an anticholinergic.
A. Hypothermia D. a barbiturate.
B. Hyperventilation
C. Tinnitus
D. Tachycardia 33. Recent international guidelines
recommend that mild, episodic asthma be
treated initially with:
29. When dispensing a prescription for
methotrexate, the pharmacist should A. inhaled corticosteroids.
recommend which of the following B. inhaled 2 -agonists.
supplements? C. oral theophylline.
D. oral corticosteroids.
A. Iron
B. Folic acid
C. Riboflavin
D. Cyanocobalamin 34. Results of blood cultures of a 37-year-old
IV drug abuser who has endocarditis
reveal Staphylococcus aureus resistant to
30. Which of the following medications is oxacillin. An appropriate
least likely to interfere with oral antistaphylococcal agent for this patient
contraceptives? would be:

Sample Questions
A. Phenytoin
B. Topiramate A. nafcillin.
C. Lamotrigine B. vancomycin.
D. Oxcarbazepine C. erythromycin.
D. chloramphenicol.

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35. Seventy-two of 100 consecutive patients 39. The major clinical complications of
who were admitted to a hospital for ethylene glycol ingestion develop because
treatment of a first myocardial infarction of:
smoked cigarettes. Why would it be
inappropriate to conclude that smoking is
A. direct toxicity caused by the
a risk factor for myocardial infarction? substance.
B. toxicity caused by the active
A. An insufficient number of patients
metabolites.
were evaluated. C. hypoxia caused by the substance.
B. There was no control group. D. cardiovascular instability caused by
C. The duration of cigarette smoking
the metabolites.
was not determined.
D. The gender and race of the patients
was not evaluated.
40. Cyanide produces its toxic action by
tightly binding with which of the
36. In a patient receiving enteral nutrition via following enzyme systems?
nasogastric tube, which of the following is
most helpful in preventing aspiration
pneumonia? A. Monoamine oxidase
B. Cytochrome oxidase
C. Acetylcholine esterase
A. Elevating the head of the bed during D. Glucose 6-phosphate dehydrogenase
feeding
B. Adding methylene blue to the enteral
formula
C. Feeding as bolus rather than as
continuous infusions
D. Administering prophylactic
antibiotics

37. Which of the following is most likely to


be toxic if ingested by a child?

A. Barium sulfate
B. Crayons
C. Oil of wintergreen
D. Glycerol

38. The tonic-clonic seizures associated with


idiopathic status epilepticus may result in:

A. persistent hypoxia of the central


nervous system.
B. abscess in the central nervous system.
C. transient ischemic attack.
D. brain tumor.

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Answer Key

Area I Area III


1 C 21 B
2 D 22 C
3 A 23 A
4 A 24 A
5 A 25 B
6 D 26 A
7 D
8 D
Area IV
27 C
Area II 28 A
9 D 29 B
10 D 30 C
11 D 31 C
12 D 32 C
13 B 33 B
14 B 34 B
15 C 35 B
16 A 36 A
17 C 37 C
18 B 38 A
19 A 39 B
20 B 40 B

Answer Key

13
14
Textbooks Commonly Used in
US Pharmacy Schools

The following is a suggested reading list. It does not Cipolle RJ, Strand LM, Morley PC. Pharmaceutical
claim to include all textbooks used in US pharmacy Care Practice: The Clinicians Guide. 2nd ed.
schools but is a guide for your preparation. Many of the McGraw-Hill Medical; 2004.
books on this list have been published in more than one
Connors KA, Amidon GL, Stella VJ. Chemical
edition. Please consult a bookstore or a health sciences
Stability of Pharmaceuticals: A Handbook for
librarian for more detailed information.
Pharmacists. 2nd ed. Wiley-Interscience; 1986.
Anderson PO. Handbook of Clinical Drug Data. 10th Conway TW, Spector AA, Chappell D, Montgomery
ed. McGraw-Hill Medical; 2001. R (Ed). Biochemistry: A Case-Oriented Approach.
6th ed. C.V. Mosby; 1996.
Ansel HC, Allen LV, Popovich NG. Pharmaceutical
Dosage Forms and Drug Delivery Systems. 8th ed. Delvin TM. Textbook of Biochemistry with Clinical
Lippincott Williams & Wilkins; 2004. Correlations. 6th ed. Wiley-Liss; 2006.
Ansel HC, Stoklosa MJ. Pharmaceutical Calculations. Dennerll JT, Davis PE. Medical Terminology: A
12th ed. Lippincott Williams & Wilkins; 2006. Programmed Systems Approach. 9th ed, Thomson
Delmar Learning; 2004.
Banker GS, Rhodes CT, Eds. Modern Pharmaceutics,
Drugs & the Pharmaceutical Sciences. 4th ed. DiPiro JT, Talbert RL, Yee GC, et al.
Marcel Dekker; 2004 Pharmacotherapy: A Pathophysiologic Approach.
6th ed. McGraw-Hill Medical; 2005.
Berardi RR, Kroon L, McDermott J, et al. Handbook
of Nonprescription Drugs. 15th ed. APhA Fink JL. Pharmacy Law Digest, 2006: The Definitive
Publications; 2006. Source of Pharmacy Law. 40th ed. Facts and
Comparisons; 2005.
Berg JM, Stryer L, Tymoczko JL. Biochemistry. 5th ed.
W.H. Freeman ; 2002. Ganong WF. Review of Medical Physiology. 22nd ed.
McGraw-Hill Medical; 2005.
Block J, Wilson CO, Beale JM, Gisvold O, Eds.
Wilson and Gisvold’s Textbook of Organic Gilbert DN, Moellering RC, Eliopoulos GM, Sande
Medicinal and Pharmaceutical Chemistry. 11th ed. MA. The Sanford Guide to Antimicrobial Therapy,
Lippincott Williams and Wilkins; 2004. 2005. 35th ed. Antimicrobial Therapy, Inc; 2005.
Bodenheimer T, Grumbach K. Understanding Health Gossel TA, Bricker JD. Principles of Clinical
Policy: A Clinical Approach. 4th ed. McGraw-Hill Toxicology. 3rd ed. CRC Press; 1994.
2005. Katzung BG. Basic & Clinical Pharmacology. 9th ed.
in US Pharmacy Schools
Textbooks Commonly Used
Bootman JL, Townsend RJ, McGhan WF, Eds. McGraw-Hill Medical; 2003.
Principles of Pharmacoeconomics. 3rd ed. Harvey Koda-Kimble MA, Young LY, Kradjan WA, Guglielmo
Whitney Books Company, 2004. BJ, Alldredge BK, Corelli RL, Eds. Applied
Borgsdorf LR, Selevan JR, Cada DJ, (Eds), et al. Drug Therapeutics: The Clinical Use of Drugs. 8th ed.
Facts and Comparisons 60th Ed. 2006. Lippencott Lippencott Williams & Wilkins; 2004.
Williams & Wilkins; 2004 Kumar V, Fausto N, Abbus A. Robbins & Cotran
Brunton L, Lazo J, Parker K. Goodman and Gilman’s Pathologic Basis of Disease. 7th ed. W.B. Saunders
The Pharmacological Basis of Therapeutics. 11th Company; 2004.
ed. McGraw-Hill Professional; 2005. Lemke TL. Review of Organic Functional Groups:
Carstensen JT. Pharmaceutical Principles of Solid Introduction to Medicinal Organic Chemistry. 4th
Dosage Forms. CRC Press; 1993. ed. Lippincott Williams & Wilkins; 2003.

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Biochemistry. 4th ed. W.H. Freeman; 2004. Communication Skills in Pharmacy Practice: A
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Preamble and Mission Statement of the
National Association of Boards of Pharmacy
Preamble
Given that medications are an integral part of disease management, medication therapies and their delivery systems
are becoming more complex, technological enhancements have improved the capabilities for patient monitoring, and
entities motivated by economic gain are eroding standards of care, there is greater potential harm to the public and
a greater need for patients’ medication use to be managed by a licensed pharmacist and state regulatory agencies to
aggressively enforce standards of care.

NABP Mission Statement


The National Association of Boards of Pharmacy (NABP) is the independent, international, and impartial
Association that assists its member boards and jurisdictions in developing, implementing, and enforcing uniform
standards for the purpose of protecting the public health.

NABP Member Boards of Pharmacy


Alabama State Board of Pharmacy Michigan Board of Pharmacy Virgin Islands Board of Pharmacy
Alaska Board of Pharmacy Minnesota Board of Pharmacy Virginia Board of Pharmacy
Arizona State Board of Pharmacy Mississippi Board of Pharmacy Washington State Board of Pharmacy
Arkansas State Board of Pharmacy Missouri Board of Pharmacy West Virginia Board of Pharmacy
California State Board of Pharmacy Montana Board of Pharmacy Wisconsin Pharmacy Examining Board
Colorado State Board of Pharmacy Nebraska Board of Pharmacy Wyoming State Board of Pharmacy
Connecticut Commission of Pharmacy Nevada State Board of Pharmacy Australia:
Delaware State Board of Pharmacy New Hampshire Board of Pharmacy Pharmacy Board of New South Wales*
District of Columbia Board of Pharmacy New Jersey Board of Pharmacy Pharmacy Board of Victoria*
Florida Board of Pharmacy New Mexico Board of Pharmacy Canada:
Georgia State Board of Pharmacy New York State Board of Pharmacy Alberta College of Pharmacists*
Guam Board of Examiners for Pharmacy North Carolina Board of Pharmacy College of Pharmacists of British
Hawaii State Board of Pharmacy North Dakota State Board of Pharmacy Columbia*

Idaho Board of Pharmacy Ohio State Board of Pharmacy Manitoba Pharmaceutical Association*

Illinois Department of Financial and Oklahoma State Board of Pharmacy New Brunswick Pharmaceutical
Professional Regulation, Division of Oregon State Board of Pharmacy Society*
Professional Regulation – State Board Nova Scotia College of Pharmacists*
of Pharmacy Pennsylvania State Board of Pharmacy
Puerto Rico Board of Pharmacy Ontario College of Pharmacists*
Indiana Board of Pharmacy
Rhode Island Board of Pharmacy Prince Edward Island Pharmacy
Iowa Board of Pharmacy Examiners Board*
Kansas State Board of Pharmacy South Carolina Department of Labor,
Licensing, and Regulation – Board of Quebec Order of Pharmacists*
Kentucky Board of Pharmacy Pharmacy New Zealand:
Louisiana Board of Pharmacy South Dakota State Board of Pharmacy Pharmacy Council of New Zealand*
Maine Board of Pharmacy Tennessee Board of Pharmacy Africa:
Maryland Board of Pharmacy Texas State Board of Pharmacy South African Pharmacy Council*
Massachusetts Board of Registration Utah Board of Pharmacy
in Pharmacy * Associate Member
Vermont Board of Pharmacy

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National Association of Boards of Pharmacy
1600 Feehanville Drive
Mount Prospect, IL 60056
847/391-4406
www.nabp.net

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