100 Most Important Nepal Pharmacy Council Exam past Questions (part-1)

Aanand Singh
1

Preparing for the Nepal Pharmacy Council licensing examination requires a good understanding of pharmacology, pharmacokinetics, therapeutics, pharmaceutical chemistry, and other core pharmacy subjects.

Practice questions are useful for revision, but understanding the reason behind each answer is more valuable than memorizing answers alone. The following questions are designed as an educational revision resource based on important pharmacy topics commonly studied for pharmacy licensing examinations.

For additional examination preparation, you can also read our article on Nepal Pharmacy Council Website Model Questions with Answers – Part 1.

Pharmacokinetics and General Pharmacology

1. Most drugs are absorbed primarily by which mechanism?

A. Active transport
B. Passive diffusion
C. Endocytosis
D. Pinocytosis

Answer: B. Passive diffusion

Explanation: Most drugs cross biological membranes mainly by passive diffusion, moving from a region of higher concentration to lower concentration.

2. Which route of administration provides 100% bioavailability?

A. Oral
B. Intravenous
C. Intramuscular
D. Rectal

Answer: B. Intravenous

Explanation: Intravenous administration delivers the drug directly into systemic circulation, so bioavailability is considered 100%.

nepal-pharmacy-council-past-question

3. Which route commonly undergoes hepatic first-pass metabolism?

A. Rectal
B. Oral
C. Intravenous
D. Sublingual

Answer: B. Oral

Explanation: Many orally administered drugs enter the portal circulation after absorption and pass through the liver before reaching systemic circulation.

4. What is an important feature of the sublingual route?

A. Slow absorption
B. Relatively rapid absorption
C. Extensive first-pass metabolism
D. No absorption

Answer: B. Relatively rapid absorption

Explanation: The sublingual mucosa has a good blood supply, allowing rapid absorption of suitable drugs and avoiding the usual hepatic first-pass effect.

5. Weakly acidic drugs may be absorbed from which site?

A. Oral cavity
B. Stomach
C. Intestine
D. Esophagus

Answer: B. Stomach

Explanation: Weak acids may have a greater unionized fraction in acidic environments. However, many drugs are still absorbed predominantly from the small intestine because of its large surface area.

6. Hyoscine is commonly absorbed after oral administration mainly from the:

A. Intestine
B. Stomach
C. Esophagus
D. Oral cavity

Answer: A. Intestine

Explanation: Like many orally administered drugs, absorption mainly occurs through the small intestine because of its large absorptive surface.

7. Aspirin is a weak acid and can be absorbed from the:

A. Intestine
B. Stomach
C. Esophagus
D. Oral cavity

Answer: B. Stomach

Explanation: Aspirin can be absorbed from the stomach because acidic conditions favor a greater unionized fraction. Significant absorption may also occur in the small intestine.

8. Most orally administered drugs are absorbed predominantly from the:

A. Stomach
B. Ileum
C. Small intestine
D. Large intestine

Answer: C. Small intestine

Explanation: The small intestine has a large surface area, extensive blood supply, and favorable conditions for absorption.

9. Alkalinization of urine generally increases the excretion of:

A. Weakly basic drugs
B. Weakly acidic drugs
C. Neutral drugs
D. Strong bases

Answer: B. Weakly acidic drugs

Explanation: Alkaline urine increases ionization of weak acids, reducing tubular reabsorption and increasing urinary excretion.

10. The most important organ for drug metabolism is the:

A. Stomach
B. Liver
C. Kidney
D. Intestine

Answer: B. Liver

Explanation: The liver is the major site of metabolism for many medicines because it contains numerous drug-metabolizing enzymes.

11. Which organs play an important role in drug excretion?

A. Kidney and rectum
B. Stomach and kidney
C. Skin and liver
D. Lungs and liver

Answer: C. Skin and liver

Explanation: Drugs and metabolites may be eliminated through several routes. The kidney is the major excretory organ, while the liver eliminates some substances through bile. Skin and lungs may also contribute to elimination.

12. A major microsomal enzyme system involved in drug metabolism is:

A. Cytochrome P450
B. Decarboxylase
C. Transferase
D. Transpeptidase

Answer: A. Cytochrome P450

Explanation: Cytochrome P450 enzymes metabolize many medicines and are important in drug interactions.

13. Oxidation and reduction reactions are generally associated with which phase of metabolism?

A. Phase I
B. Phase II
C. Phase III
D. Phase IV

Answer: A. Phase I

Explanation: Phase I reactions commonly include oxidation, reduction, and hydrolysis.

14. Which phase of metabolism is commonly called the conjugation phase?

A. Phase I
B. Phase II
C. Phase III
D. Phase IV

Answer: B. Phase II

Explanation: Phase II reactions include conjugation processes such as glucuronidation, sulfation, and acetylation.

15. Which of the following is NOT a recognized basic type of drug action?

A. Stimulation
B. Depression
C. Simulation
D. Irritation

Answer: C. Simulation

Explanation: Stimulation, depression, irritation, replacement, and cytotoxic action are traditional classifications of drug action. Simulation is not generally listed as a separate basic type.

16. The rate and extent to which an unchanged drug reaches systemic circulation is called:

A. Absorption
B. Metabolism
C. Excretion
D. Bioavailability

Answer: D. Bioavailability

Explanation: Bioavailability describes the extent and rate at which the active drug reaches systemic circulation.

17. Bioavailability is commonly represented by which symbol?

A. BA
B. F
C. BE
D. M

Answer: B. F

Explanation: Absolute bioavailability is commonly represented by the symbol F.

18. The therapeutic index mainly provides information about a drug's:

A. Potency
B. Safety margin
C. Color
D. Solubility

Answer: B. Safety margin

Explanation: The therapeutic index compares toxic and effective doses and provides an indication of the safety margin.

19. Drugs that bind to receptors but do not produce a pharmacological response are called:

A. Agonists
B. Antagonists
C. Full agonists
D. Enzyme inducers

Answer: B. Antagonists

Explanation: Antagonists bind to receptors but do not activate them and may block the effects of agonists.

20. Which type of adverse drug reaction is predictable and dose-dependent?

A. Type A
B. Type B
C. Type C
D. Type D

Answer: A. Type A

Explanation: Type A reactions are usually dose-related and predictable from the known pharmacological action of the drug.

21. Posology is the study of:

A. Poisons
B. Drug dosage
C. Microorganisms
D. Drug packaging

Answer: B. Drug dosage

Explanation: Posology is the branch of pharmacology concerned with the study of drug doses.

22. "What the body does to the drug" refers to:

A. Pharmacodynamics
B. Pharmacokinetics
C. Pharmacovigilance
D. Posology

Answer: B. Pharmacokinetics

Explanation: Pharmacokinetics includes absorption, distribution, metabolism, and excretion of drugs.

Gastrointestinal Drugs and NSAIDs

23. Triple therapy is commonly used for the management of:

A. Helicobacter pylori infection
B. Tuberculosis
C. Leprosy
D. Dermatitis

Answer: A. Helicobacter pylori infection

Explanation: H. pylori treatment commonly uses a combination of acid suppression and appropriate antimicrobial therapy according to current guidelines.

24. Which antibiotic is NOT part of the most common standard H. pylori triple-therapy combinations?

A. Metronidazole
B. Clarithromycin
C. Tetracycline
D. Amoxicillin

Answer: C. Tetracycline

Explanation: Traditional triple therapy commonly uses a proton pump inhibitor with clarithromycin and amoxicillin or metronidazole. Treatment recommendations can vary according to resistance patterns.

25. Simethicone is mainly used as a:

A. Antacid
B. Ulcer protective agent
C. Antibiotic
D. Antiflatulent

Answer: D. Antiflatulent

Explanation: Simethicone reduces the surface tension of gas bubbles and helps relieve symptoms associated with flatulence.

26. Antacids can interfere with the action of which medicine because of pH-related effects?

A. H2-receptor antagonists
B. Proton pump inhibitors
C. Sucralfate
D. Anticholinergics

Answer: C. Sucralfate

Explanation: Sucralfate requires an acidic environment for optimal action, so changes in gastric pH can affect its performance.

27. Which H2-receptor antagonist is known for inhibition of cytochrome P450 enzymes?

A. Ranitidine
B. Famotidine
C. Cimetidine
D. Roxatidine

Answer: C. Cimetidine

Explanation: Cimetidine can inhibit several CYP enzymes and may cause clinically important drug interactions.

28. PPI stands for:

A. Protein Pump Inhibitor
B. Proton Pump Inhibitor
C. Proton Pump Inducer
D. Protein Pathway Inhibitor

Answer: B. Proton Pump Inhibitor

Explanation: PPIs reduce gastric acid secretion by inhibiting the gastric H+/K+-ATPase proton pump.

29. Which is an example of a systemic antacid?

A. Aluminium hydroxide
B. Sodium bicarbonate
C. Magnesium hydroxide
D. Magnesium trisilicate

Answer: B. Sodium bicarbonate

Explanation: Sodium bicarbonate is absorbable and is traditionally classified as a systemic antacid.

30. Which H2-receptor antagonist is known to be moisture sensitive?

A. Famotidine
B. Ranitidine
C. Roxatidine
D. Cimetidine

Answer: B. Ranitidine

Explanation: Ranitidine formulations historically required appropriate protection from environmental conditions. Note that ranitidine availability has changed in many countries because of NDMA-related concerns.

31. Which combination is commonly used in antacid preparations?

A. Aluminium hydroxide and magnesium hydroxide
B. Co-trimoxazole and magnesium hydroxide
C. Naloxone and aluminium hydroxide
D. Metronidazole and magnesium hydroxide

Answer: A. Aluminium hydroxide and magnesium hydroxide

Explanation: Combining aluminium and magnesium salts can help balance gastrointestinal effects because aluminium may cause constipation while magnesium may cause diarrhea.

32. Aspirin primarily acts by inhibiting:

A. Lipoxygenase
B. Cyclooxygenase
C. Phospholipase
D. Transpeptidase

Answer: B. Cyclooxygenase

Explanation: Aspirin irreversibly inhibits cyclooxygenase enzymes, reducing prostaglandin and thromboxane synthesis.

33. Which medicine can produce a hepatotoxic metabolite in overdose?

A. Tetracycline
B. Ranitidine
C. Paracetamol
D. Allopurinol

Answer: C. Paracetamol

Explanation: Excess paracetamol can produce the toxic metabolite NAPQI, especially when normal detoxification pathways are overwhelmed.

34. What is the antidote for significant paracetamol overdose?

A. Desferrioxamine
B. Activated charcoal only
C. N-acetylcysteine
D. Naloxone

Answer: C. N-acetylcysteine

Explanation: N-acetylcysteine helps replenish glutathione and reduces toxicity from NAPQI.

35. A common adverse effect of ibuprofen and other NSAIDs is:

A. GI irritation
B. Severe hypoglycemia
C. Cataract formation
D. Hair growth

Answer: A. GI irritation

Explanation: NSAIDs can reduce protective prostaglandins in the gastrointestinal tract and may cause irritation, ulcers, or bleeding.

Gout and Rheumatoid Arthritis

36. Excess uric acid can lead to:

A. Rheumatoid arthritis
B. Gout
C. Peptic ulcer
D. Hyperlipidemia

Answer: B. Gout

Explanation: Deposition of monosodium urate crystals in joints can cause gout.

37. Which medicine has traditionally been used for acute gout attacks?

A. Allopurinol
B. Colchicine
C. Probenecid
D. NSAIDs such as indomethacin

Answer: D. NSAIDs such as indomethacin

Explanation: NSAIDs are commonly used for acute gout, while colchicine is also an important option. Choice depends on the patient's clinical condition and contraindications.

38. Which medicine is used to reduce uric acid production in chronic gout?

A. Allopurinol
B. Colchicine
C. Indomethacin
D. Ibuprofen

Answer: A. Allopurinol

Explanation: Allopurinol inhibits xanthine oxidase and reduces uric acid production.

39. A common adverse effect of colchicine is:

A. Constipation
B. Diarrhea
C. Hyperglycemia
D. Bradycardia

Answer: B. Diarrhea

Explanation: Gastrointestinal adverse effects, particularly diarrhea, are common with colchicine.

40. A commonly used low-dose colchicine tablet strength is:

A. 0.1 mg
B. 0.5 mg or 0.6 mg
C. 0.06 mg
D. 10 mg

Answer: B. 0.5 mg or 0.6 mg

Explanation: Colchicine tablet strength varies by country and manufacturer. Dosing should always follow current prescribing guidance.

41. Gold salts were historically used in the treatment of:

A. Gout
B. Rheumatoid arthritis
C. Myasthenia gravis
D. Hyperlipidemia

Answer: B. Rheumatoid arthritis

Explanation: Gold compounds were historically used as disease-modifying treatments for rheumatoid arthritis but are now much less commonly used.

Endocrinology and Diabetes

42. Which is the primary male sex hormone?

A. Testosterone
B. Estrogen
C. Progesterone
D. Estradiol

Answer: A. Testosterone

Explanation: Testosterone is the principal androgen hormone in males.

43. STD stands for:

A. Sexually Transmitted Disease
B. Standard Therapeutic Dose
C. Sterile Tablet Dosage
D. Systemic Toxic Dose

Answer: A. Sexually Transmitted Disease

Explanation: STD is a commonly used abbreviation for sexually transmitted disease, although STI is also widely used.

44. Calcitonin is primarily produced by the:

A. Thyroid gland
B. Parathyroid gland
C. Adrenal gland
D. Pituitary gland

Answer: A. Thyroid gland

Explanation: Calcitonin is produced by parafollicular or C cells of the thyroid gland.

45. Thyroid-stimulating hormone is secreted by the:

A. Thyroid gland
B. Anterior pituitary
C. Posterior pituitary
D. Parathyroid gland

Answer: B. Anterior pituitary

Explanation: TSH is secreted by the anterior pituitary and stimulates the thyroid gland.

46. Which hormone primarily stimulates breast milk production?

A. Oxytocin
B. Prolactin
C. Vasopressin
D. Calcitonin

Answer: B. Prolactin

Explanation: Prolactin stimulates milk production, while oxytocin is involved in milk ejection.

47. Diabetes insipidus may occur because of deficiency of:

A. Insulin
B. Glucagon
C. ADH
D. Somatostatin

Answer: C. ADH

Explanation: Central diabetes insipidus is associated with insufficient production or release of antidiuretic hormone.

48. In which type of diabetes mellitus is there severe deficiency of endogenous insulin due to beta-cell destruction?

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

Answer: A. Type 1

Explanation: Type 1 diabetes results from autoimmune destruction of pancreatic beta cells in most cases.

49. Insulin is commonly administered for routine treatment by which route?

A. Intramuscular
B. Intravenous
C. Subcutaneous
D. Oral

Answer: C. Subcutaneous

Explanation: Most insulin products are routinely administered subcutaneously.

50. Insulin is produced by which pancreatic cells?

A. Alpha cells
B. Gamma cells
C. Delta cells
D. Beta cells

Answer: D. Beta cells

Explanation: Pancreatic beta cells synthesize and secrete insulin.

51. Diabetic ketoacidosis is commonly managed with:

A. Lispro only
B. Aspart only
C. Glulisine only
D. Regular insulin

Answer: D. Regular insulin

Explanation: Intravenous regular insulin is commonly used in DKA protocols together with fluid and electrolyte management.

52. In emergency situations such as DKA, regular insulin may be administered by:

A. Subcutaneous route only
B. Intramuscular route only
C. Intravenous route
D. Oral route

Answer: C. Intravenous

Explanation: IV regular insulin is commonly used in DKA management according to approved clinical protocols.

53. Which medicine is commonly considered first-line for many patients with type 2 diabetes?

A. Glyburide
B. Metformin
C. Acarbose
D. Sitagliptin

Answer: B. Metformin

Explanation: Metformin is widely recommended as an important first-line medicine, although treatment should be individualized.

54. Metformin is generally recommended to be taken:

A. Before meals
B. After meals only
C. With meals
D. On an empty stomach

Answer: C. With meals

Explanation: Taking metformin with food can help reduce gastrointestinal adverse effects.

55. Human insulin contains how many amino acids?

A. 51
B. 41
C. 31
D. 21

Answer: A. 51

Explanation: Human insulin contains 51 amino acids distributed between the A and B chains.

Lipids, Vitamins and Nutrition

56. A desirable total cholesterol level for most adults is generally:

A. Less than 250 mg/dL
B. Less than 200 mg/dL
C. Less than 100 mg/dL
D. Less than 500 mg/dL

Answer: B. Less than 200 mg/dL

Explanation: A total cholesterol level below 200 mg/dL is generally considered desirable, although cardiovascular risk assessment involves multiple factors.

57. Shorter-acting statins are often taken:

A. In the morning
B. At bedtime
C. At noon
D. Only before exercise

Answer: B. At bedtime

Explanation: Cholesterol synthesis is higher at night, so shorter-acting statins may be more effective when taken in the evening. Some longer-acting statins can be taken at any convenient time.

58. Which lipoprotein is commonly called "good cholesterol"?

A. LDL
B. HDL
C. IDL
D. VLDL

Answer: B. HDL

Explanation: HDL participates in reverse cholesterol transport, although cardiovascular risk is more complex than simply increasing HDL levels.

59. Which lipoprotein mainly transports cholesterol from the liver to peripheral tissues?

A. LDL
B. HDL
C. VLDL
D. IDL

Answer: A. LDL

Explanation: LDL transports cholesterol to peripheral tissues and elevated LDL is an important cardiovascular risk factor.

60. All of the following are fat-soluble vitamins EXCEPT:

A. Vitamin K
B. Vitamin C
C. Vitamin E
D. Vitamin D

Answer: B. Vitamin C

Explanation: Vitamins A, D, E, and K are fat soluble, whereas vitamin C is water soluble.

61. Scurvy occurs due to deficiency of:

A. Vitamin K
B. Vitamin C
C. Vitamin A
D. Vitamin E

Answer: B. Vitamin C

Explanation: Vitamin C deficiency impairs collagen formation and can lead to scurvy.

62. Which vitamin is known for an important antioxidant role?

A. Vitamin E
B. Biotin
C. Vitamin A only
D. Vitamin D

Answer: A. Vitamin E

Explanation: Vitamin E, particularly tocopherols, has important antioxidant activity.

63. Which vitamin is used to reverse excessive anticoagulant effects of warfarin in appropriate clinical situations?

A. Vitamin K
B. Vitamin C
C. Vitamin A
D. Vitamin D

Answer: A. Vitamin K

Explanation: Vitamin K can help restore synthesis of vitamin K-dependent clotting factors.

64. Deficiency of which vitamin may cause osteomalacia in adults?

A. Vitamin K
B. Vitamin A
C. Vitamin D
D. Vitamin C

Answer: C. Vitamin D

Explanation: Vitamin D deficiency impairs bone mineralization and can cause osteomalacia.

65. Beriberi is caused by deficiency of:

A. Vitamin K
B. Vitamin B1
C. Vitamin B3
D. Vitamin B5

Answer: B. Vitamin B1

Explanation: Beriberi results from thiamine deficiency.

66. Pellagra is caused by deficiency of:

A. Vitamin C
B. Vitamin B5
C. Niacin
D. Biotin

Answer: C. Niacin

Explanation: Niacin deficiency causes pellagra, classically associated with dermatitis, diarrhea, and dementia.

67. The approximate energy value of fat is:

A. 9 kcal/g
B. 7 kcal/g
C. 4 kcal/g
D. 5 kcal/g

Answer: A. 9 kcal/g

Explanation: Fat provides approximately 9 kilocalories per gram.

68. Which is a rich plant-based source of protein?

A. Soybean
B. Rice
C. Sugar
D. Butter

Answer: A. Soybean

Explanation: Soybeans are rich in protein and are an important plant protein source.

69. The building blocks of proteins are:

A. Saccharides
B. Carbohydrates
C. Amino acids
D. Fatty acids

Answer: C. Amino acids

Explanation: Proteins are polymers made from amino acids joined by peptide bonds.

Cardiovascular Drugs and Diuretics

70. Renin is primarily secreted by the:

A. Liver
B. Kidney
C. Stomach
D. Lungs

Answer: B. Kidney

Explanation: Renin is released by juxtaglomerular cells in the kidneys.

71. A common adverse effect of ACE inhibitors is:

A. Dry cough
B. Hair growth
C. Hyperuricemia
D. Cataract

Answer: A. Dry cough

Explanation: ACE inhibition can increase bradykinin levels, contributing to a persistent dry cough.

72. Ankle swelling is a common adverse effect of:

A. Amitriptyline
B. Amlodipine
C. Famotidine
D. Omeprazole

Answer: B. Amlodipine

Explanation: Peripheral edema is a common adverse effect of dihydropyridine calcium-channel blockers.

73. Which strengths of amlodipine are commonly available?

A. 5 mg, 10 mg, 15 mg
B. 2.5 mg, 5 mg, 10 mg
C. 10 mg, 20 mg, 50 mg
D. 100 mg, 200 mg, 500 mg

Answer: B. 2.5 mg, 5 mg, 10 mg

Explanation: These strengths are commonly marketed, although availability can vary by country.

74. The usual route of administration of nifedipine is:

A. Oral
B. Sublingual
C. Subcutaneous
D. Rectal

Answer: A. Oral

Explanation: Nifedipine is generally administered orally. Immediate-release sublingual use is not recommended because of safety concerns.

75. Which calcium-channel blocker has a benzothiazepine structure?

A. Diltiazem
B. Verapamil
C. Amlodipine
D. Nifedipine

Answer: A. Diltiazem

Explanation: Diltiazem is classified as a benzothiazepine calcium-channel blocker.

76. A common effect of furosemide may include:

A. Ankle edema
B. Muscle cramps
C. Severe constipation
D. Hypercalcemia

Answer: B. Muscle cramps

Explanation: Furosemide can cause electrolyte loss, which may contribute to muscle cramps and weakness.

77. Acetazolamide acts by inhibiting:

A. Transpeptidase
B. Carbonic anhydrase
C. Phospholipase
D. Cyclooxygenase

Answer: B. Carbonic anhydrase

Explanation: Acetazolamide is a carbonic anhydrase inhibitor and is also used for certain indications including prevention of acute mountain sickness.

78. Propranolol should generally be avoided or used with great caution in:

A. Hypertension
B. Angina
C. Bronchial asthma
D. Migraine

Answer: C. Bronchial asthma

Explanation: Propranolol blocks beta-2 receptors and may cause bronchoconstriction.

79. Which beta-blocker is relatively short acting?

A. Propranolol
B. Timolol
C. Esmolol
D. Atenolol

Answer: C. Esmolol

Explanation: Esmolol has a very short duration of action and is commonly used intravenously in acute clinical settings.

80. Which medicine has historically been used for hypertension during pregnancy?

A. Amlodipine
B. Furosemide
C. Methyldopa
D. Aliskiren

Answer: C. Methyldopa

Explanation: Methyldopa has a long history of use in pregnancy. Current treatment choices depend on guidelines and individual clinical circumstances.

81. Which diuretic may cause gynecomastia?

A. Amiloride
B. Furosemide
C. Hydrochlorothiazide
D. Spironolactone

Answer: D. Spironolactone

Explanation: Spironolactone has antiandrogenic effects and can cause gynecomastia.

82. Which is a potent loop diuretic?

A. Thiazide
B. Furosemide
C. Amlodipine
D. Nifedipine

Answer: B. Furosemide

Explanation: Furosemide is a loop diuretic and produces powerful diuresis.

83. Which is an osmotic diuretic?

A. Mannitol
B. Furosemide
C. Spironolactone
D. Amiloride

Answer: A. Mannitol

Explanation: Mannitol increases osmotic pressure within renal tubules and promotes water excretion.

84. The active metabolite of enalapril is:

A. Enalaprilat
B. Losartan
C. Captopril
D. Amlodipine

Answer: A. Enalaprilat

Explanation: Enalapril is a prodrug that is converted to enalaprilat.

85. Which drug class is commonly used as an alternative when an ACE inhibitor causes cough?

A. Losartan
B. Amlodipine
C. Spironolactone
D. Amiloride

Answer: A. Losartan

Explanation: Losartan is an angiotensin II receptor blocker and does not usually cause bradykinin-related cough.

86. Which drug has an extremely short plasma half-life?

A. Sodium nitroprusside
B. Amiloride
C. Amlodipine
D. Losartan

Answer: A. Sodium nitroprusside

Explanation: Sodium nitroprusside has a very rapid onset and short duration, making continuous IV administration necessary.

87. Which is a plant-derived antihypertensive alkaloid?

A. Reserpine
B. Amlodipine
C. Methyldopa
D. Mannitol

Answer: A. Reserpine

Explanation: Reserpine is an alkaloid obtained from Rauwolfia species and depletes catecholamine stores.

Antimicrobial Drugs

88. Sulfonamide therapy originated historically from the discovery of:

A. Protosil
B. Prontosil
C. Fungus
D. Bacteria

Answer: B. Prontosil

Explanation: Prontosil was an early sulfonamide antibacterial prodrug and an important development in antimicrobial therapy.

89. Silver sulfadiazine is commonly used for:

A. Oral infection
B. Cancer
C. Burn wound management
D. Diarrhea

Answer: C. Burn wound management

Explanation: Silver sulfadiazine has historically been used topically for prevention and treatment of infection in burn wounds.

90. The standard ratio of sulfamethoxazole to trimethoprim in co-trimoxazole is:

A. 5:1
B. 6:2
C. 7:1
D. 1:7

Answer: A. 5:1

Explanation: Co-trimoxazole contains sulfamethoxazole and trimethoprim in a 5:1 ratio by weight.

91. Which drug is historically associated with the term "magic bullet" in early antimicrobial chemotherapy?

A. Tetracycline
B. Penicillin
C. Sulfonamides
D. Chloramphenicol

Answer: C. Sulfonamides

Explanation: The concept of a "magic bullet" originated with Paul Ehrlich and selective antimicrobial chemotherapy. Early sulfonamide discoveries were major milestones in this field.

92. Patients receiving co-trimoxazole may be advised to maintain adequate fluid intake to reduce the risk of:

A. Crystal-related urinary problems
B. Hair loss
C. Cataract
D. Bradycardia

Answer: A. Crystal-related urinary problems

Explanation: Adequate hydration can help reduce the risk of crystalluria with sulfonamide-containing medicines.

93. A possible adverse effect of sulfonamide therapy is:

A. Crystalluria
B. Complete blindness in all patients
C. Permanent hair growth
D. Severe hypoglycemia in all patients

Answer: A. Crystalluria

Explanation: Some sulfonamides can precipitate in urine, particularly when hydration is inadequate.

94. Stevens-Johnson syndrome is a serious adverse reaction that can be associated with:

A. Pantoprazole
B. Sulfonamides
C. Saline solution
D. All vitamins

Answer: B. Sulfonamides

Explanation: Sulfonamides are among the medicines associated with severe cutaneous adverse reactions, including Stevens-Johnson syndrome.

95. A delayed skin reaction developing after prolonged drug exposure may involve which type of hypersensitivity?

A. Type I
B. Type II
C. Type III
D. Type IV

Answer: D. Type IV

Explanation: Type IV hypersensitivity is delayed and mediated primarily by T cells.

96. Which antibiotic has historically been called the "queen of antibiotics" in some pharmacy examination materials?

A. Penicillin
B. Chloramphenicol
C. Tetracycline
D. Pantoprazole

Answer: B. Chloramphenicol

Explanation: This is a traditional examination term. Chloramphenicol has broad antibacterial activity but its use is limited because of serious potential toxicity.

97. Penicillin was discovered by Alexander Fleming in:

A. 1928
B. 1940
C. 1950
D. 1945

Answer: A. 1928

Explanation: Alexander Fleming observed the antibacterial effect of Penicillium mold in 1928.

98. Who is widely known as the discoverer of penicillin?

A. Alexander Fleming
B. Louis Pasteur
C. Robert Koch
D. Paul Ehrlich

Answer: A. Alexander Fleming

Explanation: Alexander Fleming discovered penicillin, while later scientists including Howard Florey and Ernst Chain contributed significantly to its clinical development.

99. Penicillin was first widely developed for clinical use around:

A. 1929
B. 1941
C. 1945
D. 1948

Answer: B. 1941

Explanation: Penicillin began to be used clinically in the early 1940s after successful purification and development work.

100. Which of the following is a natural penicillin?

A. Ampicillin
B. Benzylpenicillin (Penicillin G)
C. Amoxicillin
D. Cloxacillin

Answer: B. Benzylpenicillin (Penicillin G)

Explanation: Benzylpenicillin is a natural penicillin. Ampicillin and amoxicillin are semisynthetic penicillins.

Quick Revision Tips

When preparing for the Nepal Pharmacy Council licensing examination, do not memorize only the correct option. Try to understand the mechanism, indication, adverse effect, or scientific principle behind each answer.

Important areas for revision include:

  • Drug absorption and bioavailability
  • Drug metabolism and excretion
  • Pharmacodynamics and adverse drug reactions
  • Gastrointestinal pharmacology
  • NSAIDs and analgesics
  • Gout and rheumatoid arthritis
  • Diabetes and endocrine pharmacology
  • Vitamins and nutrition
  • Cardiovascular drugs and diuretics
  • Antimicrobial pharmacology

For more pharmacy examination practice, you can also read Nepal Pharmacy Council Past Questions – Part 2.

Students preparing for pharmaceutical analysis can also read Pharmaceutical Analysis MCQ-1 for Nepal Pharmacy Council Exam and Pharmaceutical Analysis MCQ-2 with Answers.

For students interested in pharmaceutical industry work and Quality Control, our article on Quality Control Test of Tablet in Pharmaceutical Industry provides useful information about pharmaceutical product testing.

Conclusion

Past and practice questions are useful tools for pharmacy examination preparation, but conceptual understanding is essential for long-term success.

This collection of 100 important questions covers several fundamental areas of pharmacology and therapeutics. Students should revise the scientific principles behind the answers, consult standard pharmacy textbooks, and follow current clinical and examination guidance where applicable.

References

  1. Katzung BG. Basic and Clinical Pharmacology.

  2. Rang HP, Ritter JM, Flower RJ, Henderson G. Rang and Dale's Pharmacology.

  3. Brunton LL, Hilal-Dandan R, Knollmann BC. Goodman & Gilman's The Pharmacological Basis of Therapeutics.

  4. Tripathi KD. Essentials of Medical Pharmacology.

  5. Standard pharmacy textbooks and current academic resources relevant to pharmacy licensing examinations.

Disclaimer

This article is intended for educational and examination-preparation purposes only. It is not an official Nepal Pharmacy Council question paper. Drug recommendations and clinical guidelines may change over time, and students should verify important information using current textbooks, official guidance, and reliable academic resources.

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