Pharmacist Prometric exam questions
Therapeutics, calculations, compounding, law and pharmacovigilance.
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Every regulator: format, pass marks and fees for all GCC licensing exams, each from the regulator's own documents.
The Pharmacist exam at a glance
DHA (UAE) publishes a Pharmacist exam of 150 MCQs in 3 hours with a 60% pass mark; DOH (UAE) publishes a Pharmacist exam of 50-100 MCQs in 1-2 hours, scored pass or fail; SCFHS (Saudi Arabia) publishes a Pharmacist exam of 200 MCQs in 240 minutes with a 536 on a 200-800 scale pass mark; QCHP (Qatar) publishes a Pharmacist exam of 150 MCQs in 3 hours with a 60% pass mark; OMSB (Oman) publishes a Pharmacist exam of 100 MCQs in 150 minutes with a 60% pass mark. MOHAP, SHA, NHRA do not publish Pharmacist-specific figures; their regulator-wide format and pass-mark rules are in the full table. Kuwait MOH publishes no exam for this title.
- DHA · UAE
- Pharmacist (PHO5481)
- 150 MCQs in 3 hours · pass mark 60% · USD 240 (about AED 880) · checked September 2026
- DOH · UAE
- Pharmacist CBT
- 50-100 MCQs in 1-2 hours · pass mark Pass / fail only · AED 550 · checked October 2026
- SCFHS · Saudi Arabia
- Saudi Pharmacist Licensure Examination (SPLE)
- 200 MCQs in 240 minutes · pass mark 536 on a 200-800 scale · checked October 2026
- QCHP · Qatar
- Pharmacist
- 150 MCQs in 3 hours · pass mark 60% · checked September 2026
- OMSB · Oman
- Omani Examination for Pharmacists (OEP)
- 100 MCQs in 150 minutes · pass mark 60% · USD 200 (about OMR 80) · checked September 2026
From each regulator's own exam documents; the DHA row is from the DHA CBT Guideline, Sep 2026. Every other regulator is in the full GCC table.
Try two questions from this bank
Original questions from the bank - pick an answer to see the rationale and reference.
A chemotherapy agent is ordered at 50 mg/m² for a patient with a body surface area of 1.6 m². What is the calculated dose?
Choose an answer to see the rationale.
A TPN order requires 50 g of dextrose. Using a 70% dextrose stock solution, what volume is needed?
Choose an answer to see the rationale.
Not sure where you stand? Sit 25 of these questions free, timed at real exam pace, and see which domains you are weakest in.
Take the free mock exam →Liked those? The full bank has 549 questions at this standard - every one with a rationale and a reference.
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- ✓3 to 6 full-length papers (~135 Q each)
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- ✓Four options, one unambiguous best answer
- ✓A full rationale on every question
- ✓A real guideline or textbook reference
- ✓Every sub-topic in the published blueprint
- ✓Researched by Neelim's exam research team
- ✓Prepared for your authority's exam, not a generic set
The Pharmacist exam in every GCC country
| Regulator | Exam | Format | Pass mark | Fee per attempt |
|---|---|---|---|---|
Pharmacist (PHO5481) | 150 MCQs in 3 hours | 60% | USD 240 (about AED 880) | |
Pharmacist CBT | 50-100 MCQs in 1-2 hours | Pass / fail only | AED 550 | |
| 200 MCQs in 240 minutes | 536 on a 200-800 scale | Not published | ||
Pharmacist | 150 MCQs in 3 hours | 60% | Not published | |
Omani Examination for Pharmacists (OEP) | 100 MCQs in 150 minutes | 60% | USD 200 (about OMR 80) | |
MOHAP licensing exam Regulator-wide format | Computer-based | Not published | Not published | |
SHA licensing exam Regulator-wide format | Set at assessment | Not published | Not published | |
NHRA licensing exam Regulator-wide format | Prometric CBT | Not published | Not published | |
No exam published for this title Kuwait MOH publishes no exam for this title; check with the MOH | Not published | Not published | Not published |
Highlighted rows publish figures for this exact Pharmacist exam; the others show the regulator's general rules.
From each regulator's own exam pages; anything a regulator does not publish says so. Assessment mode also depends on your licence title, so confirm your route on your eligibility notice.
Try 30 free Pharmacist questions with answersDifferent from the samples on this page - each with a full explanationStart →What the Pharmacist exam covers
The published blueprint for this exam breaks into 13 domains and 183 testable sub-topics. Our bank covers every one of them - here is the full map, so you can see exactly what you are expected to know.
Clinical Therapeutics & Disease-State Management~30% (DHA lists 'Pharmaceutical Care & Disease State Management' at 35%; SCFHS Clinical Sciences 35%)22 topics
- Hypertension: JNC/ACC-AHA staging, first-line agents (thiazides, ACEi, ARB, CCB), compelling indications, resistant HTN, hypertensive emergency
- Dyslipidemia: statin intensity, LDL/ASCVD risk, ezetimibe, PCSK9 inhibitors, fibrates, statin myopathy monitoring
- Ischemic heart disease, acute coronary syndrome, antiplatelets (aspirin, clopidogrel, ticagrelor), nitrates
- Heart failure (HFrEF/HFpEF): ACEi/ARNI, beta-blockers, MRAs, SGLT2i, diuretics, digoxin
- Arrhythmias and anticoagulation: atrial fibrillation, warfarin (INR, interactions, reversal), DOACs, heparin/LMWH, VTE treatment and prophylaxis
- Diabetes mellitus type 1 & 2: ADA targets/HbA1c, metformin, sulfonylureas, DPP-4i, GLP-1 RA, SGLT2i, insulin regimens, hypoglycemia, DKA/HHS
- +16 more in the bank
Pharmacology, Drug Classes, ADRs & Drug Interactions~12% (est.; core of SCFHS Pharmaceutical Sciences 35%)15 topics
- Mechanisms of action across major drug categories including biologics
- Pharmacodynamics: receptor theory, agonists/antagonists, dose-response, potency vs efficacy, therapeutic index
- Autonomic pharmacology: cholinergic, anticholinergic, adrenergic and antiadrenergic agents
- Cardiovascular, renal and diuretic pharmacology
- CNS pharmacology: sedatives, anesthetics, antiepileptics, antidepressants, antipsychotics
- Endocrine pharmacology: insulin, oral hypoglycemics, thyroid, corticosteroids, sex hormones
- +9 more in the bank
Pharmaceutical Calculations & Compounding~12% (DHA 'Pharmacy Calculation & Compounding' 15%; SCFHS Sterile/Nonsterile Compounding)15 topics
- Systems of measurement, metric conversions, and household equivalents
- Concentration expressions: percentage strength (w/w, w/v, v/v), ratio strength, ppm
- Dilution and concentration, alligation medial and alligation alternate
- Dosage and dose calculations by body weight and body surface area (BSA)
- Pediatric dose calculations (Clark's, Young's rules) and mg/kg dosing
- IV flow rate, drip rate (gtt/min), and infusion time calculations
- +9 more in the bank
Pharmaceutics, Biopharmaceutics & Pharmacokinetics~8% (est.; SCFHS Pharmaceutics 2.4 & Pharmacokinetics 2.5)15 topics
- Dosage form design: solid, liquid, semisolid, controlled/modified release, patches, implants
- Biopharmaceutical principles of drug delivery and release from dosage forms
- Physicochemical properties affecting drug entities and dosage forms (solubility, partition coefficient, pKa)
- Materials, excipients and methods used in dosage-form preparation
- Drug and dosage-form stability: chemical degradation kinetics and physical instability
- Principles of biotechnology-derived products and their application
- +9 more in the bank
Medicinal Chemistry, Pharmacognosy & Dietary Supplements~6% (est.; SCFHS Medicinal Chemistry 2.1 & Pharmacognosy 2.3)11 topics
- Physicochemical properties of drugs in relation to ADME
- Chemical basis for drug action and fundamental pharmacophores by disease
- Structure-activity relationships and drug-receptor interactions
- Chemical pathways of drug metabolism (phase I and phase II)
- Application of SAR to drug-therapy decisions
- Crude drugs, semi-purified and purified natural products
- +5 more in the bank
Basic Biomedical Sciences~6% (SCFHS Basic Biomedical Sciences 10%)13 topics
- Physiology: function of major body systems and homeostasis at organ/system level
- Biochemistry of biomacromolecules: proteins, lipids, carbohydrates, nucleic acids
- Intermediary and energy metabolism and nutritional molecules
- Enzymology, coenzymes and enzyme kinetics
- Cell chemistry and signal transduction pathways
- DNA/RNA science, protein synthesis and molecular genetics
- +7 more in the bank
Nonprescription (OTC) & Self-Care / Counter Medication~6% (DHA 'Counter Medication' 10%)12 topics
- Triage and identifying when to refer to a physician vs self-treat
- Analgesics and antipyretics OTC (paracetamol/acetaminophen, ibuprofen dosing and limits)
- Cough, cold and allergy products; decongestants and antihistamines
- Gastrointestinal OTC: antacids, laxatives, antidiarrheals, antiemetics
- Dermatologic OTC: antifungals, hydrocortisone, acne, wound care
- Ophthalmic and otic OTC products
- +6 more in the bank
Special Populations~5% (DHA lists Pregnancy/Lactation 5%, Pediatrics 5%, Geriatrics 5%)12 topics
- Pregnancy: drug safety categories, teratogens, and managing chronic conditions in pregnancy
- Lactation: drug transfer into breast milk and compatible/incompatible medications
- Neonatal and pediatric pharmacotherapy: weight-based dosing and developmental pharmacokinetics
- Pediatric formulation and palatability considerations
- Geriatric pharmacotherapy: physiologic changes affecting PK/PD
- Beers Criteria and potentially inappropriate medications in the elderly
- +6 more in the bank
Toxicology & Poisoning Management~5% (DHA Toxicology 5%; SCFHS acute/chronic toxicity)12 topics
- Acute and chronic drug and chemical overdose principles
- Common poisonings and specific antidotes (paracetamol/N-acetylcysteine, opioids/naloxone, benzodiazepines/flumazenil)
- Anticoagulant reversal (vitamin K, protamine, idarucizumab, andexanet)
- Organophosphate poisoning (atropine, pralidoxime) and cholinergic toxidromes
- Heavy-metal poisoning and chelation therapy (lead, iron/deferoxamine, mercury, arsenic)
- Methanol/ethylene glycol (fomepizole, ethanol) and toxic alcohols
- +6 more in the bank
Patient Assessment, Counseling, Drug Information & Evidence-Based Practice~5% (est.; SCFHS Clinical 4.1, 4.5 & Professional Communication 3.8)14 topics
- Obtaining a comprehensive patient and medication history
- Performing and interpreting patient physical assessment findings
- Interpreting clinical laboratory values and diagnostic tests
- Identifying and prioritizing drug-related problems
- Medication therapy management (MTM) and medication reconciliation
- Patient counseling technique on all pharmaceutical agents, storage and administration
- +8 more in the bank
Pharmacy Law, Ethics & Regulatory Affairs~6% (DHA Law & Ethics 10%; SCFHS 3.5 & 3.7)14 topics
- Legal and regulatory principles applied to dispensing and professional services
- Controlled substances and narcotics regulations, scheduling and record-keeping
- Prescription-only vs nonprescription vs controlled medication classification
- Authority and role of health authorities (DHA, DOH, MOHAP, SCFHS/SFDA, QCHP, NHRA, OMSB)
- Pharmacy licensing, registration and DataFlow verification requirements
- Prescription requirements, validity and dispensing rules in the GCC
- +8 more in the bank
Public Health, Pharmacoeconomics, Pharmacoepidemiology & Biostatistics~5% (est.; SCFHS Social/Behavioral/Administrative 3.1-3.3, 3.6)14 topics
- Organization of health-care delivery systems in the GCC
- Social, political and economic factors influencing health-care delivery
- Public health and wellness: chronic-disease prevention, health promotion, infectious-disease control
- Demographics and environmental factors leading to disease
- Role of immunizations in disease prevention and health promotion
- Pharmacoepidemiology: data sources and study designs to estimate benefit/risk in populations
- +8 more in the bank
Pharmacy Practice Management, Medication Safety & Dispensing Systems~5% (DHA Medication Safety 5%; SCFHS 3.4 & 3.10)14 topics
- Management principles: planning, organizing, directing and controlling pharmacy resources
- Inventory management, procurement, storage and cold-chain requirements
- Marketing, pricing, distribution and promotion of pharmacy products/services
- Accounting, budgeting and financial management
- Systems for safe and effective preparation and dispensing across practice settings
- Pharmacy informatics, automation and information-management technology
- +8 more in the bank
12 worked Pharmacist practice questions
Original exam-style questions from the bank, spread across the blueprint domains. They are not real or recalled exam questions. Try each one, then open the answer for the rationale and reference. None of them appear in the free mock exam, so reading them will not spoil it.
Question 1 · Clinical Therapeutics & Disease-State Management
A patient with HIV is being counseled that antiretroviral therapy involves a combination regimen rather than a single drug. What is the primary rationale for using combination antiretroviral therapy (typically three active agents)?
- ATo reduce the number of daily tablets to one
- BTo maximally suppress viral replication and prevent emergence of resistance
- CTo eliminate the need for adherence to therapy
- DTo cure the infection completely within weeks
Show answer and explanation
Correct answer: B. To maximally suppress viral replication and prevent emergence of resistance
Combination antiretroviral therapy using agents from different classes achieves durable maximal viral suppression and prevents the emergence of drug resistance that would occur rapidly with monotherapy. ART controls but does not cure HIV, adherence remains essential, and pill burden reduction is a formulation convenience rather than the core rationale.
Reference: DHHS Guidelines for the Use of Antiretroviral Agents in Adults and Adolescents with HIV 2023; WHO HIV guidelines
Question 2 · Pharmaceutical Calculations & Compounding
A disinfectant is prepared at a ratio strength of 1:2500. What is this concentration expressed in parts per million (ppm)?
- A40 ppm
- B250 ppm
- C400 ppm
- D2500 ppm
Show answer and explanation
Correct answer: C. 400 ppm
A ratio strength of 1:2500 means 1 part in 2500 parts; dividing 1,000,000 by 2500 gives 400 ppm. The other options misplace the decimal or invert the ratio.
Reference: Ansel's Pharmaceutical Calculations, 15th ed. (2017)
Question 3 · Medicinal Chemistry, Pharmacognosy & Dietary Supplements
Levodopa is used in Parkinson's disease rather than dopamine itself. Which combined rationale best explains this choice?
- ADopamine is a prodrug that must be converted to levodopa peripherally
- BDopamine crosses the blood-brain barrier more readily than levodopa
- CLevodopa is the inactive D-isomer that is safer than dopamine
- DLevodopa is an amino-acid prodrug that crosses the blood-brain barrier via an active transporter and is then decarboxylated to dopamine centrally
Show answer and explanation
Correct answer: D. Levodopa is an amino-acid prodrug that crosses the blood-brain barrier via an active transporter and is then decarboxylated to dopamine centrally
Dopamine does not cross the blood-brain barrier, so its metabolic precursor levodopa (L-DOPA) is given as a prodrug; being an amino acid, it is carried across the barrier by the large neutral amino-acid transporter and is then decarboxylated to dopamine within the CNS. It is the pharmacologically relevant L-isomer (not the inactive D-form), and it is levodopa, not dopamine, that penetrates the brain.
Reference: Katzung Basic & Clinical Pharmacology, 15th ed. (2021), antiparkinsonian drugs
Question 4 · Nonprescription (OTC) & Self-Care / Counter Medication
A patient presents with a minor superficial skin abrasion. Which self-care wound advice is most appropriate?
- AApply undiluted hydrogen peroxide daily to the healing wound
- BClean gently with water, keep it moist and covered, and refer if signs of infection develop
- CLeave it uncovered and apply an oral antibiotic
- DApply a potent topical corticosteroid to speed healing
Show answer and explanation
Correct answer: B. Clean gently with water, keep it moist and covered, and refer if signs of infection develop
Minor abrasions should be gently cleaned (e.g., with clean water), kept moist and covered to promote healing, with referral if signs of infection (spreading redness, pus, fever) appear. Repeated undiluted hydrogen peroxide damages healing tissue, oral antibiotics are unnecessary for a simple abrasion, and topical corticosteroids can impair wound healing.
Reference: Handbook of Nonprescription Drugs (APhA), 2021 - Minor wound care; NICE CKS Lacerations
Question 5 · Special Populations
A 24-year-old woman with epilepsy controlled on valproate wishes to become pregnant. Regarding valproate use in pregnancy, which statement is most accurate?
- AValproate carries the highest risk of neural tube defects and impaired neurodevelopment among common antiepileptics
- BValproate is considered the safest antiepileptic in pregnancy
- CFolic acid supplementation eliminates the teratogenic risk of valproate
- DValproate should be switched to phenytoin, which is non-teratogenic
Show answer and explanation
Correct answer: A. Valproate carries the highest risk of neural tube defects and impaired neurodevelopment among common antiepileptics
Valproate has the highest teratogenic risk among common antiepileptics, causing neural tube defects and a dose-dependent reduction in childhood IQ/neurodevelopment, so it should be avoided in women of childbearing potential when alternatives exist. Folic acid reduces but does not eliminate neural tube defect risk. Phenytoin is also teratogenic (fetal hydantoin syndrome), so it is not a non-teratogenic substitute.
Reference: NICE Epilepsy Guideline NG217 (2022); MHRA Valproate Pregnancy Prevention Programme
Question 6 · Patient Assessment, Counseling, Drug Information & Evidence-Based Practice
When appraising a randomized controlled trial for internal validity, which methodological feature MOST directly reduces the risk of selection bias?
- AAllocation concealment during randomization
- BUsing a large sample size
- CReporting results as relative risk
- DPublishing in a high-impact journal
Show answer and explanation
Correct answer: A. Allocation concealment during randomization
Allocation concealment prevents those enrolling participants from knowing or influencing the next assignment, directly protecting against selection bias and ensuring comparable groups at baseline. A large sample improves precision but not freedom from bias, and the choice of effect measure or journal prestige does not address internal validity. Concealed allocation is a core determinant of a trial's methodological quality.
Reference: Higgins et al., Cochrane Handbook for Systematic Reviews of Interventions, 2019
Question 7 · Pharmacy Practice Management, Medication Safety & Dispensing Systems
According to USP <800>, which engineering control is required for compounding sterile hazardous drugs to protect both the preparation and the operator?
- AA horizontal laminar airflow bench blowing air toward the operator
- BA containment primary engineering control such as a biological safety cabinet or compounding aseptic containment isolator, in a negative-pressure room
- CAn open workbench with a desk fan
- DA standard fume hood vented into the pharmacy
Show answer and explanation
Correct answer: B. A containment primary engineering control such as a biological safety cabinet or compounding aseptic containment isolator, in a negative-pressure room
USP <800> requires sterile hazardous-drug compounding within a containment primary engineering control (for example, a Class II biological safety cabinet or compounding aseptic containment isolator) located in an externally vented, negative-pressure containment area to protect both product sterility and the worker. A horizontal laminar bench blows contaminants toward the operator, and open benches, desk fans, or internally recirculating hoods provide no adequate containment.
Reference: USP General Chapter <800> Hazardous Drugs - Handling in Healthcare Settings (2020)
Question 8 · Pharmacology, Drug Classes, ADRs & Drug Interactions
A 65-year-old man with a history of tendon disorders needs treatment for a urinary infection. Which class carries a black-box warning for tendinitis and tendon rupture that should influence antibiotic choice?
- AFluoroquinolones
- BMacrolides
- CFirst-generation cephalosporins
- DNitrofurantoin
Show answer and explanation
Correct answer: A. Fluoroquinolones
Fluoroquinolones carry black-box warnings including tendinitis and tendon rupture (risk increased in older patients and with concurrent corticosteroids), so alternatives are preferred when possible. Macrolides, cephalosporins, and nitrofurantoin do not carry this specific tendon-rupture warning.
Reference: US FDA Drug Safety Communication on fluoroquinolones (2016, updated)
Question 9 · Pharmaceutics, Biopharmaceutics & Pharmacokinetics
A drug is a weak acid that is filtered and undergoes passive tubular reabsorption. In an overdose, alkalinizing the urine with sodium bicarbonate enhances its elimination. What is the mechanism?
- AAlkaline urine converts the acid to its unionized form, increasing reabsorption
- BAlkalinization inhibits active tubular secretion of the drug
- CAlkalinization increases glomerular filtration rate directly
- DAlkaline urine ionizes the weak acid, trapping it in the tubular lumen and reducing reabsorption
Show answer and explanation
Correct answer: D. Alkaline urine ionizes the weak acid, trapping it in the tubular lumen and reducing reabsorption
Raising urinary pH ionizes a weak acid (such as salicylate or phenobarbital); the ionized species is lipid-insoluble and cannot be passively reabsorbed, so it is trapped in the tubular lumen and excreted more rapidly (ion trapping). Alkalinization does not primarily change GFR or active secretion, and it decreases, not increases, reabsorption.
Reference: Katzung, Basic & Clinical Pharmacology, 15th ed., 2021
Question 10 · Basic Biomedical Sciences
A microbiology report describes an acid-fast bacillus that resists standard Gram staining because of its lipid-rich cell wall and requires the Ziehl-Neelsen stain. This staining property is due to a high content of which cell-wall component?
- ATeichoic acid
- BLipopolysaccharide
- CMycolic acid
- DLipoteichoic acid
Show answer and explanation
Correct answer: C. Mycolic acid
Acid-fast organisms such as Mycobacterium species have cell walls rich in mycolic acids (long-chain fatty acids), which make them resist decolorization by acid-alcohol and require the Ziehl-Neelsen technique. Teichoic and lipoteichoic acids are gram-positive wall components, and lipopolysaccharide is a gram-negative outer-membrane component; none confer acid-fastness.
Reference: Murray Medical Microbiology, 9th ed., 2021
Question 11 · Pharmacy Law, Ethics & Regulatory Affairs
Which of the following adverse events should most clearly be prioritized for expedited pharmacovigilance reporting?
- AA serious, unexpected reaction such as an unlabeled anaphylactic or hepatotoxic event, especially with a newly marketed medicine
- BA mild, well-documented transient headache from a long-established drug
- CA patient's dislike of a tablet's taste
- DA minor, self-limiting reaction already described in the product label
Show answer and explanation
Correct answer: A. A serious, unexpected reaction such as an unlabeled anaphylactic or hepatotoxic event, especially with a newly marketed medicine
Serious and unexpected (not previously labeled) reactions, particularly with newer medicines, warrant expedited reporting because they may reflect important new safety signals. Mild, well-characterized, expected, or trivial events such as taste complaints carry far less surveillance value and do not require expedited reporting.
Reference: CIOMS/WHO pharmacovigilance reporting standards; WHO Pharmacovigilance guidance (2002)
Question 12 · Special Populations
A patient is a CYP2C19 poor metabolizer. Which antiplatelet drug's effectiveness is most likely reduced, prompting consideration of an alternative agent after PCI?
- AClopidogrel
- BPrasugrel
- CTicagrelor
- DAspirin
Show answer and explanation
Correct answer: A. Clopidogrel
Clopidogrel is a prodrug requiring CYP2C19 activation; poor metabolizers form less active drug, reducing antiplatelet effect and increasing cardiovascular events, so prasugrel or ticagrelor (not CYP2C19-dependent) are preferred alternatives. Aspirin acts by an unrelated mechanism (COX inhibition) and is unaffected by CYP2C19 status.
Reference: CPIC Guideline for Clopidogrel and CYP2C19 (2013, updated 2022)
Pharmacist reference books and guidelines
Every question in this bank names the textbook or guideline its answer rests on. These are the sources our Pharmacist questions cite most often - the reading list to revise from alongside the bank.
Textbooks
10- 1
Ansel's Pharmaceutical Calculations
16th edition - 2
Handbook of Nonprescription Drugs (APhA)
2021 - 3
Guyton and Hall Textbook of Medical Physiology
14th edition2020 - 4
Goldfrank's Toxicologic Emergencies
11th edition2019 - 5
Katzung Basic & Clinical Pharmacology
15th edition2021 - 6
Lehninger Principles of Biochemistry
8th edition2021 - 7
Goodman & Gilman's The Pharmacological Basis of Therapeutics
14th edition2023 - 8
Foye's Principles of Medicinal Chemistry
8th edition2019 - 9
Trease and Evans' Pharmacognosy
16th edition2009 - 10
Sinko, Martin's Physical Pharmacy and Pharmaceutical Sciences
7th edition2016
Guidelines and standards
10- 1
AHA/ACC/HFSA Heart Failure Guideline
2022 - 2
WHO Adherence to Long-Term Therapies
2003 - 3
AHA/ACC Cholesterol Guideline
2018 - 4
Endocrine Society Hypertriglyceridemia Guideline
2012 - 5
WHO Guide to Good Prescribing
1994 - 6
ESC Heart Failure Guidelines
2021 - 7
ACC/AHA Stable Ischemic Heart Disease Guideline
2014 - 8
KDIGO Diabetes in CKD Guideline
2022 - 9
DHHS Guidelines for the Use of Antiretroviral Agents in Adults and Adolescents with HIV
2023 - 10
NICE Epilepsy Guideline
NG2172022
Sitting the SPLE? SCFHS publishes its own list: SCFHS's SPLE reading list. Where your regulator publishes a reading list, use the editions it names. Exam questions are not taken from any one book.
Last reviewed September 2026
About these questions: every question is original, researched by Neelim's exam research team, written to the published blueprint, with a rationale and a reference. No recalled or leaked exam content is used. How we write our questions.
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