Disorders of blood MCQs With Answer

Introduction: Disorders of blood MCQs With Answer provide B. Pharm students a focused, clinically relevant review of hematology concepts including anemia types, leukemias, coagulation disorders, platelet dysfunction, transfusion reactions, and laboratory markers. This set emphasizes pathophysiology, diagnostic tests (MCV, MCHC, reticulocyte count, PT/aPTT, D-dimer, ferritin), and pharmacotherapy (iron therapy, folate/B12, anticoagulants, hydroxyurea, colony-stimulating factors, chelators, targeted agents). Designed to deepen understanding of erythrocyte and platelet biology, hemostasis, and drug mechanisms, these MCQs link basic science to therapeutic decisions—helpful for exams and clinical pharmacy practice. Now let’s test your knowledge with 30 MCQs on this topic.

Q1. Which laboratory parameter best indicates the average red blood cell size?

  • Mean corpuscular volume (MCV)
  • Mean corpuscular hemoglobin concentration (MCHC)
  • Red cell distribution width (RDW)
  • Reticulocyte count

Correct Answer: Mean corpuscular volume (MCV)

Q2. A right shift of the oxygen-hemoglobin dissociation curve is promoted by which factor?

  • Decreased 2,3-BPG
  • Increased 2,3-BPG
  • Decreased temperature
  • Alkalosis

Correct Answer: Increased 2,3-BPG

Q3. The most reliable laboratory indicator of depleted iron stores is:

  • High serum ferritin
  • Low serum ferritin
  • High transferrin saturation
  • Increased hemoglobin A2

Correct Answer: Low serum ferritin

Q4. Vitamin B12 deficiency typically produces which hematologic picture?

  • Microcytic hypochromic anemia
  • Normocytic normochromic anemia
  • Macrocytic megaloblastic anemia
  • Sideroblastic anemia

Correct Answer: Macrocytic megaloblastic anemia

Q5. Which laboratory findings are characteristic of hemolytic anemia?

  • Decreased lactate dehydrogenase (LDH)
  • Increased haptoglobin
  • Increased indirect bilirubin
  • Low reticulocyte count

Correct Answer: Increased indirect bilirubin

Q6. The molecular defect responsible for sickle cell disease is a substitution of which amino acid in beta-globin?

  • Valine to glutamic acid
  • Glutamic acid to valine
  • Glycine to alanine
  • Proline to serine

Correct Answer: Glutamic acid to valine

Q7. Hydroxyurea benefits patients with sickle cell disease primarily by:

  • Reducing leukocyte counts only
  • Acting as an iron chelator
  • Increasing fetal hemoglobin (HbF) production
  • Directly inhibiting hemoglobin polymerization

Correct Answer: Increasing fetal hemoglobin (HbF) production

Q8. Beta-thalassemia major hemoglobin electrophoresis typically shows:

  • Predominant HbA with low HbF
  • Increased HbF and increased HbA2
  • Only HbS present
  • Elevated HbA2 only

Correct Answer: Increased HbF and increased HbA2

Q9. The activated partial thromboplastin time (aPTT) assesses which coagulation pathway?

  • Extrinsic pathway
  • Intrinsic pathway
  • Common pathway only
  • Platelet function

Correct Answer: Intrinsic pathway

Q10. Warfarin exerts its anticoagulant effect by inhibiting:

  • Antithrombin III
  • Vitamin K epoxide reductase (VKORC1)
  • Factor Xa directly
  • Platelet aggregation

Correct Answer: Vitamin K epoxide reductase (VKORC1)

Q11. Unfractionated heparin anticoagulant activity primarily involves activation of:

  • Protein C
  • Antithrombin III
  • Plasminogen
  • Factor XIII

Correct Answer: Antithrombin III

Q12. Rivaroxaban is an oral anticoagulant that directly inhibits which target?

  • Thrombin (Factor IIa)
  • Factor Xa
  • Vitamin K epoxide reductase
  • Platelet P2Y12 receptor

Correct Answer: Factor Xa

Q13. The laboratory test used to monitor warfarin therapy is:

  • Activated partial thromboplastin time (aPTT)
  • Thrombin time (TT)
  • Prothrombin time / International Normalized Ratio (PT/INR)
  • D-dimer

Correct Answer: Prothrombin time / International Normalized Ratio (PT/INR)

Q14. Disseminated intravascular coagulation (DIC) typically shows which laboratory pattern?

  • Low D-dimer and high fibrinogen
  • High fibrinogen and normal platelets
  • Elevated D-dimer and low fibrinogen
  • Isolated prolonged aPTT only

Correct Answer: Elevated D-dimer and low fibrinogen

Q15. Immune thrombocytopenic purpura (ITP) is caused by autoantibodies directed against:

  • Factor VIII
  • Platelet glycoproteins (e.g., GPIIb/IIIa)
  • Fibrinogen
  • Red cell membrane proteins

Correct Answer: Platelet glycoproteins (e.g., GPIIb/IIIa)

Q16. The primary site of erythropoietin production in adults is the:

  • Bone marrow stromal cells
  • Liver hepatocytes
  • Renal peritubular interstitial cells
  • Spleen macrophages

Correct Answer: Renal peritubular interstitial cells

Q17. Filgrastim is a pharmaceutical form of which growth factor used to treat chemotherapy-induced neutropenia?

  • GM-CSF (granulocyte-macrophage colony-stimulating factor)
  • Erythropoietin
  • G-CSF (granulocyte colony-stimulating factor)
  • Thrombopoietin

Correct Answer: G-CSF (granulocyte colony-stimulating factor)

Q18. Aplastic anemia is characterized by which bone marrow finding?

  • Hypercellular marrow with megakaryocytic hyperplasia
  • Hypocellular marrow with fatty replacement
  • Marrow packed with blasts
  • Excess iron-laden macrophages

Correct Answer: Hypocellular marrow with fatty replacement

Q19. Acute intravascular hemolysis after an ABO-incompatible transfusion is primarily mediated by:

  • IgG causing extravascular hemolysis
  • T-cell mediated cytotoxicity
  • IgM-mediated complement activation
  • Platelet antibody binding

Correct Answer: IgM-mediated complement activation

Q20. Which chemotherapeutic or immunosuppressive drug commonly causes megaloblastic anemia by inhibiting dihydrofolate reductase?

  • Hydroxyurea
  • Methotrexate
  • Cisplatin
  • Cyclophosphamide

Correct Answer: Methotrexate

Q21. Which iron chelator is administered orally for chronic transfusional iron overload in thalassemia?

  • Deferoxamine (parenteral)
  • Deferasirox (oral)
  • Deferiprone (intravenous only)
  • EDTA (oral)

Correct Answer: Deferasirox (oral)

Q22. Glucose-6-phosphate dehydrogenase (G6PD) deficiency hemolysis can be triggered by which drug?

  • Penicillin
  • Primaquine
  • Metformin
  • Atorvastatin

Correct Answer: Primaquine

Q23. Which parameter typically rises as a compensatory response in hemolytic anemia?

  • Serum ferritin
  • Mean corpuscular volume (MCV)
  • Reticulocyte count
  • Platelet count

Correct Answer: Reticulocyte count

Q24. Prothrombin time (PT) primarily evaluates which coagulation pathway?

  • Intrinsic pathway
  • Extrinsic pathway
  • Fibrinolytic pathway
  • Platelet adhesion pathway

Correct Answer: Extrinsic pathway

Q25. Which antimicrobial agent is well-known to cause bone marrow suppression and aplastic anemia in rare cases?

  • Chloramphenicol
  • Amoxicillin
  • Ciprofloxacin
  • Metronidazole

Correct Answer: Chloramphenicol

Q26. Pernicious anemia results from autoimmune destruction of gastric parietal cells leading to deficiency of:

  • Intrinsic factor and impaired B12 absorption
  • Gastrin and decreased iron absorption
  • HCl only with normal B12 absorption
  • Pepsinogen causing folate deficiency

Correct Answer: Intrinsic factor and impaired B12 absorption

Q27. Thrombopoietin, a key regulator of platelet production, is primarily produced in the:

  • Kidney
  • Liver
  • Spleen
  • Bone marrow

Correct Answer: Liver

Q28. Paroxysmal nocturnal hemoglobinuria (PNH) involves a defect in which cell-surface proteins that protect against complement?

  • CD3 and CD4
  • CD19 and CD20
  • CD55 and CD59
  • CD8 and CD56

Correct Answer: CD55 and CD59

Q29. The direct antiglobulin (Coombs) test is used to detect:

  • Circulating free hemoglobin
  • Autoantibodies or complement bound to patient red cells
  • Serum iron levels
  • Platelet function defects

Correct Answer: Autoantibodies or complement bound to patient red cells

Q30. Imatinib, a targeted therapy used in chronic myeloid leukemia (CML), inhibits which abnormal kinase?

  • JAK2
  • BCR-ABL tyrosine kinase
  • SRC kinase only
  • FLT3 receptor

Correct Answer: BCR-ABL tyrosine kinase

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