Foreign Pharmacy Graduate Equivalency Examination — Information & Free Practice
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Foreign Pharmacy Graduate Equivalency Examination
- Provider
- National Association of Boards of Pharmacy
- Format
- Computerized fixed form
- Exam questions
- 200 questions
- Time limit
- 4.5 hours examination time; 5.5 hours total seat time
- Passing score
- Scaled score of 75
Examination outline
Foundational Biomedical Sciences (12%)
- Anatomy and physiology
- Biochemistry
- Medical microbiology
- Immunology
- Pathophysiological bases of diseases
Pharmaceutical Sciences (31%)
- Pharmaceutical calculations (eg, dose adjustments, delivery, ionization, ionic strength, isotonicity, ratio/percentage strength, osmolarity)
- Medicinal chemistry
- Medicinal chemistry: Physicochemical properties of drugs in relation to drug absorption, distribution, metabolism, and excretion (ADME)
- Medicinal chemistry: Pathways of drug metabolism
- Medicinal chemistry: Chemical bases for drug action, including bioorganic chemistry, structure-activity relationships, and fundamental pharmacophores related to drug-receptor interactions
- Medicinal chemistry: Applicability to making drug therapy decisions
- Pharmacology and toxicology
- Pharmacology and toxicology: Pharmacodynamics, including drug-receptor interactions, agonists, antagonists, inverse agonists, and dose-response curves
- Pharmacology and toxicology: Mechanisms of action of drugs, including biologics
- Pharmacology and toxicology: Adverse effects and side effects of drugs
- Pharmacology and toxicology: Mechanisms of drug interactions, including drug-drug, drug-disease, drug-food, drug-allergy, and drug-laboratory interactions
- Pharmacology and toxicology: Mechanisms of acute and chronic toxic effects of xenobiotics, including drug and chemical overdose or exposure and antidotes
- Pharmaceutics and biopharmaceutics
- Pharmaceutics and biopharmaceutics: Dosage form development and drug delivery systems such as immediate release, sustained release, and controlled release
- Pharmaceutics and biopharmaceutics: Disintegration and dissolution of solid oral dosage forms
- Pharmaceutics and biopharmaceutics: Physicochemical properties of drugs, excipients, solutions, and dosage forms
- Pharmaceutics and biopharmaceutics: Physical stability, chemical stability, and shelf-lives, including zero-, first-, second-, and pseudo-order reactions
- Pharmaceutics and biopharmaceutics: Interactions between drug formulation and biological effects
- Pharmaceutics and biopharmaceutics: Drug product manufacturing, including methods, processing, and quality assurance
- Pharmacokinetics
- Pharmacokinetics: Determining rates of absorption, distribution, metabolism, and excretion (ADME) of drugs
- Pharmacokinetics: Factors affecting rates of ADME, including age, sex, genetics, diet, disease, and drug interactions
- Pharmacokinetics: Biological half-lives of drugs and related dosing
- Pharmacokinetics: Compartment models (one-, two-, and non-)
- Pharmacokinetics: Linear and nonlinear pharmacokinetics
- Pharmacokinetics: Principles of bioavailability, bioequivalence, and biosimilars
- Pharmacogenomics (eg, population-based genetic influences on drug metabolism and efficacy, genetic testing, tumor genotyping, pharmacogenetic screening)
- Extemporaneous compounding (eg, United States Pharmacopeia (USP) standards including Chapters <795>, <797>, and <800>; dosage form preparation calculations; techniques used to prepare and dispense sterile and nonsterile preparations)
Social, Behavioral, and Administrative Sciences (20%)
- Pharmacy law and ethics
- Pharmacy law and ethics: Laws and regulations governing pharmacy
- Pharmacy law and ethics: Regulatory, oversight, and professional organizations
- Pharmacy law and ethics: Principles and application of biomedical ethics
- Health care systems
- Health care systems: Organization, regulation, and financing of health care delivery in the United States
- Health care systems: Factors that influence delivery and use of health care (eg, social, political, economic, and technological)
- Pharmacoeconomics (eg, analysis, interpretation, application, humanistic outcomes)
- Population-based care, pharmacoepidemiology, and public health
- Population-based care, pharmacoepidemiology, and public health: Data sources and analytic tools
- Population-based care, pharmacoepidemiology, and public health: Application of epidemiological study design
- Population-based care, pharmacoepidemiology, and public health: Health promotion, disease prevention, and infection control
- Population-based care, pharmacoepidemiology, and public health: Continuous quality improvement
- Population-based care, pharmacoepidemiology, and public health: Social determinants and drivers of health
- Practice management
- Practice management: Financial management and budgeting
- Practice management: Personnel management
- Practice management: Business and strategic planning
- Practice management: Risk management
- Practice management: Procurement and inventory control
- Professional communication
- Professional communication: Verbal, nonverbal, written, and technology-based communication with patients, caregivers, providers, and stakeholders
- Professional communication: Health literacy
- Biostatistics and research methods (eg, study design, statistical tests, data collection instruments, research ethics)
- Social and behavioral aspects of practice
- Social and behavioral aspects of practice: Patient behavior including health-, illness-, and sick-role
- Social and behavioral aspects of practice: Principles of behavior modification
- Social and behavioral aspects of practice: Patient adherence
- Social and behavioral aspects of practice: Cultural awareness
Pharmacy Practice and Clinical Sciences (37%)
- Clinical pathophysiology as it applies to treatment of disease processes
- Data collection (eg, patient history, physical assessments, laboratory values, point-of-care testing)
- Data assessment (eg, clinical calculations, interpretation of data, diagnosing)
- Patient-care decision making, therapy recommendations, and education (eg, plan, implement, monitor, follow-up)
- Patient safety (eg, drug interactions, toxicity, drug-induced disease, drug use disorders)
- Disease prevention (eg, screenings, immunization, non-pharmacological therapies, lifestyle modifications)
- Personalized medicine (eg, pharmacokinetics, pharmacogenetics)
- Evidence-based practice
- Evidence-based practice: Practice guidelines
- Evidence-based practice: Drug information and evaluation
- Evidence-based practice: Information source reliability
- Evidence-based practice: Clinical trial evaluation
- Self-care, including using natural products
Examination sources
- NABP FPGEE Content Outline
Detailed outline heading, page 5
- NABP FPGEE page
Prepare for the Exam, Resources
- NABP FPGEE page
Prepare for the Exam, opening paragraph
- NABP FPGEE page
Receive Results, first paragraph
- NABP FPGEE page
Register for the Exam, opening paragraph
Related license preparation
This examination may be required or accepted as an alternative, depending on the license and application pathway.