SCIENCE AND TECHNOLOGY ZARIA A. Immunological basis 100 LEVEL SECOND SEMESTER EXAMINATION B. Genetic abnormality C. Over dose of a drug SESSION: 2023/2024 12. Biotransformation facilitates the excretion of COURSE: ACTION AND USES OF COMMON drugs by changing them into; MEDICINE A. More ionized and less lipid soluble DEPARTMENT PHARMACY MARKS 60 B. Less ionized and more lipid soluble TIME: 2HRS C. More ionized and more lipid soluble Type b 13. When a drug potentiates or complements the 1. Pharmacodynamics is the study of; action of other drug the phenomenon is called; A. Preparation of drug A. Antagonism B. Biochemical and physiological effects of drug B. Drug interaction C. Toxic effect of drugs C. Synergism 14. Most drugs and metabolites are excreted by; 2. Bioavailability means the; A. The kidneys A. Rate of absorption of drugs B. The bile B. Rate and extent of absorption of drugs C. The lungs C. Rate of excretion of the drugs 15. Pharmacodynamics considers; A. The way in which the drug affects the body 3. Agonist has got; B. The effect of drug in the body and mode of action A. Affinity for the receptor C. Drug metabolism B. Efficacy 16. A drug allergy occurs; C. Affinity as well as efficacy A. When too much drug has accumulated in the body 4. If one drug antagonizes the action of other drug B. When body sees the drug as an antigen and an by interacting with different receptor, the immune response is established against the drug antagonism may be called as; C. An unwanted but predictable response to a drug A. Chemical antagonism 17. The drug receptor interaction is usually; B. Physiological antagonism A. Irreversible C. Pharmacological antagonism B. Reversible 5. Antagonism may be called as competitive if; C. Always irreversible A. Both drugs have different receptors B. Both drugs has affinity for the same receptors 18. Pharmacognosy deals with; C. Both drugs interact chemically A. Preparation of drug B. Properties and identification of drugs 6. Digoxin is obtained from; C. Doses of drugs A. Plant source B. Mineral source 19. A drug that binds to cell receptor and cause a C. Plant and synthetics response is called as; 7. Pharmacokinetics is the study of; A. Agonist A. What is drug doing to the body B. Antagonist B. What is body doing with the drug C. Receptor blocker C. What is drug doing with other drugs 20. Drugs are excreted from the body through- 8. Elimination of drug means; (a) Kidney A. Excretion of drug (b) Breast milk, saliva, sweat & bile. B. Metabolism of drugs (c) Intestine C. Metabolism and excretion of drugs (d) All of the above. 9. Protein bound drugs are; 21. the human body is known as- A. Pharmacologically inactive B. Pharmacologically more active (a) Pharmacokinetics C. Pharmacologically less active (b) Toxicology (c) Pharmacology 10. Posology deals with; (d) Pharmacodynamics A. Weighing and measuring of drug 22. Penicillin can be gotten from both natural and B. Dose and dosage semisynthetic sources? True or false C. Metabolism of drugs 23. The rate of absorption of a drug is affected by (a) Route of drug administration (b) Solubility of the drug a. 18th century (c) Site of administration b. 15th century (d) All of the above c. 19th century 24. What does “pharmacokinetics” include? d. None of the above a) Localization of drug action e. I don’t know b) Mechanisms of drug action 31. What does the term “potentiation” mean? c) Excretion of substances a) Cumulative ability of a drug d) Interaction of substances b) Hypersensitivity to a drug 25. Pharmacokinetics is: c) Fast tolerance developing a) The study of biological and therapeutic effects d) Intensive increase of drug effects due to their of drugs combination b) The study of absorption, distribution, 32. Characteristic unwanted reaction which isn’t metabolism and excretion of drugs related to a dose or to a pharmacodynamic c) The study of mechanisms of drug action property of a drug is called: d) The study of methods of new drug a) Idiosyncrasy development b) Hypersensitivity 26. The reasons determing bioavailability are: c) Tolerance a) Rheological parameters of blood d) Teratogenic action b) Amount of a substance obtained orally and 33. If one drug antagonizes the action of other drug quantity of intakes by interacting with different receptor, the c) Extent of absorption and hepatic first-pass antagonism may be called as; effect A. Chemical antagonism d) Glomerular filtration rate B. Physiological antagonism 27. Biotransformation of the drugs is to render them: C. Pharmacological antagonism a) Less ionized 34. Antagonism may be called as competitive if; b) More pharmacologically active A. Both drugs have different receptors c) More lipid soluble B. Both drugs has affinity for the same receptors d) Less lipid soluble C. Both drugs interact chemically 28. Pharmacodynamics involves the study of 35. The discipline of pharmacology dealing with following EXCEPT: mode of action of drug is known as; a) Biological and therapeutic effects of drugs A. Pharmacotherapy b) Absorption and distribution of drugs B. Pharmacy c) Mechanisms of drug action C. Pharmacodynemics d) Drug interactions 36. Drugs bound to plasma proteins; 29. Pharmacodynamics involves the following? A. Can leave vascular space a) Information about main mechanisms of drug B. Is eliminated early absorption C. Is inactive pharmacologically b) Information about unwanted effects c) Information about biological barriers d) Information about excretion of a drug from the organism 30. Pick out the answer which is the most appropriate to the term “receptor” a) All types of ion channels modulated by a drug b) Enzymes of oxidizing-reducing reactions activated by a drug c) Active macromolecular components of a cell or an organism which a drug molecule has to combine with in order to elicit its specific effect d) Carriers activated by a drug 31. Pharmacology emerged as its own discipline in ELITE INTERNATIONAL COLLEGE OF HEALTH d. Mineral SCIENCE AND TECHNOLOGY ZARIA e. chemical 100 LEVEL SECOND SEMESTER EXAMINATION 8. Which of this is as a result of immunological response SESSION: 2023/2024 a. Side effect COURSE: ACTION AND USES OF COMMON b. Depression MEDICINE c. Addiction DEPARTMENT PHARMACY MARKS 60 d. Hypersensitivity TIME: 2HRS Type a 9. One of this is not a natural sources of drugs 1. Pharmacology is __________________ a. Plant a. The study of drugs in nonliving things b. Animal b. The study of substances and their effect in c. Mineral living things d. Herbal c. The study of chemical substances in nonliving e. synthetic organism 10. The term pharmacology is derived from the word d. The study of drugs in both living and a. Pharmacon nonliving plant b. Pharmakon e. None of the above c. All of the above 2. Metabolism is_______________ d. None of the above a. A process in nonliving thing 11. The founder of modern pharmacology is b. Not biotransformation a. Oswald Schmiedeberg (1840-1926) c. The only important process that drugs b. Oswald Schmiedeberge (1833-1925) undergoes in the body c. Oswald Schmiedeberge (1838-1921) d. A process that convert drugs/medicines for d. All of the above development of new drug e. None of the above e. A parameter of pharmacokinetics 12. A substance that helps restore you to normalcy is 3. The place where a drug causes an effect to occur called? is called__________________ a. Drugs a. Site of action b. Medicines b. Site of administration c. Poisons c. Therapeutic window d. All of the above d. Minimum toxic effect e. a and b 4. Side effect is______________ 13. ………………..describes how medicines moves from a. An extension of the pharmacological effect of site of administration to the site of action a drug a. Distribution b. Not an extended pharmacological effect of the b. Metabolism drug c. Absorption c. Is the harmful effect of a drug d. Receptor affinity d. Same as idiosyncrasy e. Excretion e. Same as therapeutic effect 14. Elimination of the drug can occur through the 5. Receptor affinity is a term following except a. Referring to the ability for the receptor to a. Kidney produce response b. Skin b. Referring to the response produced by a drug c. Lungs c. Referring to the ability for a drug to bind to d. Breast milk the receptor e. Heart d. Referring to efficacy 15. All the following are sources of medicines except e. Referring to effectiveness of a drug a. Plants 6. The pharmacokinetic phase is b. Animals a. The form of the drug c. Bacterial b. The way the drug is absorbed, distributed, d. All of the above metabolized, and eliminated e. None of the above c. The effect of the drug has on the body 16. The pharmaceutical preparations in which a d. All of the above specific mixture of drug substances are presented 7. Cocaine is an example of drug from to facilitate easy and accurate administration and ____________________source delivery of active drug substances is called a. Animal a. Packed form b. Plant b. Dosage form c. Semi-synthetic c. Dose d. All of the above c) Distribution of drugs in the organism e. None of the above d) Excretion of drug from the organism 17. Food can also potentiate the effects of a drug? 28. What does “affinity” mean? True or false a) A measure of how tightly a drug binds to plasma 18. All of the following are animal sources of proteins medicine except b) A measure of how tightly a drug binds to a a. Insulin receptor b. Heparin c) A measure of inhibiting potency of a drug c. Digoxin d) A measure of bioavailability of a drug d. Cyanocobalamin 29. Which effect may lead to toxic reactions when a e. Vasopressin drug is taken continuously or repeatedly? 19. The science which deals with the drug and their a) Refractoriness action on human body is called- b) Cumulative effect (a) Physiology c) Tolerance (b) Pathology d) Tachyphylaxis (c) Pharmacology 30. What term is used to describe a more gradual (d) Microbiology decrease in responsiveness to a drug, taking 20. The study of absorption, distribution, metabolism days or weeks to develop? and excretion of drug is known as- a) Refractoriness (a) Pharmacy b) Cumulative effect (b) Pharmacokinetics c) Tolerance (c) Pharmacodynamics d) Tachyphylaxis (d) Pharmacopoeia 21. Which of the following is a source for obtaining 31. What phenomenon can occur in case of using a drugs- combination of drugs? (a) Animals and plants a) Tolerance (b) Micro-organisms b) Tachyphylaxis (c) Synthetic origin c) Accumulation (d) All of the above d) Synergism 22. What does “pharmacokinetics” include? 32. If two drugs with the same effect, taken a) Complications of drug therapy b) Drug biotransformation in the organism together, produce an effect that is equal in c) Influence of drugs on metabolism magnitude to the sum of the effects of the drugs processes given individually, it is called as: d) Influence of drugs on genes a) Antagonism 23. What does the term “bioavailability” mean? b) Potentiation 24. a) Plasma protein binding degree of substance c) Additive effect b) Permeability through the brain-blood d) None of the above barrier c) Fraction of an uncharged drug reaching the 33. Biotransformation of the drugs may lead to all of systemic circulation following any route administration the following except d) Amount of a substance in urine relative to the a) Inactive metabolite from an active drug initial doze b) Active metabolite from an active drug 25. Biotransformation of a medicinal substance c) Active metabolite from an inactive drug results in: 34. Pharmacy deals with; a) Faster urinary excretion A. Mechanism of action of drug b) Slower urinary excretion c) Easier distribution in organism B. Preparation of drug d) Higher binding to membranes C. Identification of drug 26. Pharmacodynamics involves the study of 35. 1st pass effect; following? A. Increase the bioavailability of the drugs a) Mechanisms of drug action B. Decrease the bioavailability of the drugs b) Biotransformation of drugs in the organism C. Increase the excretion of drugs c) Distribution of drugs in the organism 36. Drug allergy refers to those situations in which d) Excretion of drug from the organism 27. Pharmacodynamics involves the study of unusual response is due to; following? A. Over dose a) Mechanisms of drug action B. Wrong rout of administration b) Biotransformation of drugs in the organism C. Antigen-antibody reaction