Pharmacology — MCQs August 22, 2025 by u930973931_answers 50 Score: 0 Attempted: 0/50 Subscribe 1. The study of the effects of drugs on living systems is called: (A) Pharmacokinetics (B) Pharmacodynamics (C) Pharmacology (D) Toxicology 2. The process of drug absorption, distribution, metabolism, and excretion is known as: (A) Pharmacodynamics (B) Pharmacokinetics (C) Pharmacogenomics (D) Biopharmaceutics 3. The site of drug action is determined by its: (A) Affinity (B) Absorption (C) Distribution (D) Solubility 4. The primary organ for drug metabolism is: (A) Kidney (B) Liver (C) Intestine (D) Lung 5. The enzyme family most responsible for drug metabolism is: (A) Amylase (B) Cytochrome P450 (C) Catalase (D) Kinase 6. The main route of drug excretion is through: (A) Liver (B) Kidneys (C) Lungs (D) Skin 7. The time required for the concentration of a drug to reduce by half is: (A) Clearance (B) Bioavailability (C) Half-life (D) Steady state 8. The maximum effect a drug can produce is known as: (A) Potency (B) Efficacy (C) Affinity (D) Clearance 9. Drugs that activate receptors are called: (A) Antagonists (B) Agonists (C) Blockers (D) Inhibitors 10. Drugs that block receptors are called: (A) Antagonists (B) Agonists (C) Inducers (D) Substrates 11. A drug that produces the opposite effect of an agonist is called: (A) Partial agonist (B) Inverse agonist (C) Competitive antagonist (D) Noncompetitive antagonist 12. The study of genetic variations affecting drug response is: (A) Pharmacogenomics (B) Toxicology (C) Biopharmaceutics (D) Pharmacovigilance 13. Which route of drug administration bypasses the first-pass metabolism? (A) Oral (B) Sublingual (C) Rectal (D) Intravenous 14. The first-pass effect is primarily associated with the: (A) Liver (B) Lungs (C) Kidneys (D) Spleen 15. The therapeutic index of a drug is: (A) LD50 / ED50 (B) ED50 / LD50 (C) EC50 / ED50 (D) Clearance / Volume of distribution 16. The drug-receptor interaction is usually: (A) Covalent and irreversible (B) Ionic and reversible (C) Always covalent (D) Permanent binding 17. Which type of antagonist competes with an agonist for the same receptor site? (A) Noncompetitive (B) Irreversible (C) Competitive (D) Allosteric 18. The plasma concentration at which a drug shows maximum therapeutic effect without toxicity is: (A) Therapeutic window (B) Bioavailability (C) Steady state (D) Loading dose 19. Which phase of clinical trials evaluates drug safety in healthy volunteers? (A) Phase I (B) Phase II (C) Phase III (D) Phase IV 20. The volume of distribution (Vd) relates the drug amount in the body to: (A) Plasma concentration (B) Renal clearance (C) Half-life (D) Bioavailability 21. A drug with high first-pass metabolism should be given: (A) Intravenously (B) Orally (C) Rectally (D) Sublingually 22. The measure of how much of an administered drug reaches the systemic circulation is: (A) Clearance (B) Bioavailability (C) Potency (D) Efficacy 23. Which route of administration provides the slowest absorption? (A) Intravenous (B) Intramuscular (C) Subcutaneous (D) Oral 24. Which drug formulation provides controlled release? (A) Solution (B) Capsule (C) Enteric-coated tablet (D) Extended-release tablet 25. The term “prodrug” refers to: (A) Inactive compound converted to active form in the body (B) Active drug metabolized to inactive form (C) Drug given in maximum dose (D) Drug with no side effects 26. Tachyphylaxis refers to: (A) Increased drug response (B) Rapid tolerance to a drug (C) Prolonged half-life (D) Increased absorption 27. A side effect is defined as: (A) Unintended beneficial effect (B) Predictable, undesirable effect of drug (C) Toxic effect (D) Allergic reaction 28. An idiosyncratic drug reaction is: (A) Dose-dependent (B) Predictable (C) Genetically determined unusual response (D) Always toxic 29. The drug used as a reference standard for bioequivalence studies is called: (A) Placebo (B) Innovator drug (C) Generic drug (D) Control drug 30. A drug with zero-order kinetics is eliminated at a: (A) Constant rate (B) Variable rate (C) Proportional to plasma concentration (D) Exponential rate 31. The antidote for opioid overdose is: (A) Flumazenil (B) Naloxone (C) Atropine (D) Protamine 32. The antidote for benzodiazepine overdose is: (A) Naloxone (B) Flumazenil (C) Atropine (D) Pralidoxime 33. The drug atropine is classified as a: (A) Adrenergic agonist (B) Cholinergic agonist (C) Muscarinic antagonist (D) Nicotinic agonist 34. Beta-blockers act by blocking: (A) Alpha receptors (B) Dopamine receptors (C) Beta adrenergic receptors (D) Muscarinic receptors 35. Which type of drug interaction occurs when two drugs enhance each other’s effect? (A) Synergism (B) Antagonism (C) Potentiation (D) Idiosyncrasy 36. An example of a selective COX-2 inhibitor is: (A) Aspirin (B) Ibuprofen (C) Celecoxib (D) Diclofenac 37. The main mechanism of action of penicillin is: (A) Protein synthesis inhibition (B) DNA replication inhibition (C) Cell wall synthesis inhibition (D) RNA transcription inhibition 38. The drug digoxin acts by: (A) Inhibiting Na+/K+ ATPase (B) Stimulating adenyl cyclase (C) Blocking calcium channels (D) Enhancing beta receptors 39. A teratogenic drug causes: (A) Drug tolerance (B) Drug dependence (C) Fetal malformations (D) Allergic reactions 40. Which class of drugs is used to lower cholesterol? (A) Beta-blockers (B) ACE inhibitors (C) Statins (D) Diuretics 41. Which diuretic is potassium-sparing? (A) Furosemide (B) Hydrochlorothiazide (C) Spironolactone (D) Mannitol 42. The drug morphine acts mainly on: (A) Dopamine receptors (B) Opioid receptors (C) GABA receptors (D) Serotonin receptors 43. Which drug is used in the treatment of tuberculosis? (A) Penicillin (B) Rifampicin (C) Ciprofloxacin (D) Amoxicillin 44. Which drug is commonly used as an anticoagulant? (A) Warfarin (B) Paracetamol (C) Atorvastatin (D) Diazepam 45. Which vitamin reduces the side effects of isoniazid? (A) Vitamin A (B) Vitamin B6 (C) Vitamin B12 (D) Vitamin D 46. Which drug is used to treat hypertension by blocking calcium channels? (A) Propranolol (B) Nifedipine (C) Captopril (D) Losartan 47. Which class of drugs lowers blood pressure by blocking angiotensin-converting enzyme? (A) ARBs (B) ACE inhibitors (C) Beta-blockers (D) Diuretics 48. Insulin lowers blood glucose by promoting: (A) Lipolysis (B) Glycogenolysis (C) Glucose uptake (D) Gluconeogenesis 49. Which drug is used in asthma as a β2-adrenergic agonist? (A) Salbutamol (B) Atropine (C) Propranolol (D) Lorazepam 50. The term “pharmacovigilance” refers to: (A) Drug approval process (B) Monitoring drug safety after release (C) Studying pharmacokinetics (D) Drug formulation process