Mock Boards Module 4
Mock Boards Module 4
a. I & II
b. I, II & III
c. I & III
d. I
3. The intensity of the pharmacological action of the drug is most dependent on ____________.
b. Onset of action
c. Protein binding
d. Volume of distribution
4. Drugs with “wide” therapeutic window means that the drug is ____________.
a. Less potent
b. More potent
c. Less safe
d. More safe
5. Four identical animals were treated with mg doses of the following toxins. (refer to the choices below with their corresponding
6. Two drugs that act on the same tissue or organ through independent receptors resulting in effects of opposite directions is
known as ____________.
a. Physiologic antagonism
b. Irreversible antagonism
c. Competitive antagonism
d. Chemical antagonism
7. A drug was shown to reverse the action of a particular neurotransmitter. It appears to interact directly with the neurotransmitter
and not at all with the neurotransmitter’s receptors. Which of the following BEST describes the drug?
a. Chemical antagonist
b. Physiologic antagonist
c. Pharmacologic antagonist
d. Partial agonist
a. Physiologic antagonism
b. Competitive antagonism
c. Irreversible antagonism
d. Chemical antagonism
a. Gentamicin
b. Erythromycin
c. Doxycycline
d. Mebendazole
10. Decreased oral absorption of drug due to high stomach pH would result to:
11. Human milk is more acidic than the plasma. Which of the following statements are true given this condition?
I. Weak acid may diffuse into the breast milk and ionize.
II. Weak acid may diffuse into the breast milk and remain unionized.
III. Weak base may diffuse into the breast milk and ionize.
IV. Weak base may diffuse into the breast milk and remain unionized
a. II & III
b. II & IV
c. I & III
d. I & IV
12. Which of the following are factors affecting the systemic availability of a drug?
I. Intestinal motility
b. I & III
c. I, II & III
d. I & III
13. Which of the following is TRUE if there is a significant difference between the oral and parenteral doses of the same drug; for
14. Drugs with VERY HIGH volumes of distribution are those that have ____________.
15. Pharmaceutical equivalent drug products must have the same ____________.
a. I, II & III
b. I
c. II
d. III
16. In neonates, where there is a relative decrease in serum proteins, which of the following will be true if a highly protein bound
17. Drug metabolism happens in most cases, to convert the drug to a compound that is ____________.
I. More polar
a. II & III
b. I & IV
c. I & III
d. II & IV
a. adrenergic antagonists
b. adrenergic agonists
c. cholinergic antagonists
d. cholinergic agonists
a. Glycine Conjugation
b. Acetylation
c. Glucuronidation
d. Methylation
20. Pharmacokinetic variations in drug metabolizing enzymes (DME’s) are considered significant if ____________.
a. I & III
b. I, II & III
c. III
d. II
21. The enzyme capacity in newborns and infants is reduced. What possible effects would this have on clearance and
22. Which of the following is/are true regarding 1st order kinetics?
III. Rate of elimination is proportional to the rate of administration only at steady state.
a. II & III
b. II
c. I
d. III
23. What is the order of the reaction if the concentration of the drug is decreasing at a rate that is proportional to the
a. Zero
b. Third
c. First
d. Second
24. Which of the following refers to the process that distinguishes ethanol from the elimination of most other drugs?
b. Biliary Excretion
25. The following are true regarding patients with renal impairment EXCEPT:
a. They have reduced requirement for drugs that are directly excreted by the kidneys.
d. The serum creatinine levels are higher than the reference value.
a. II & III
b. I & IV
c. II & IV
d. I & III
27. What percent of the drug is removed per hour if the elimination rate constant is 0.25/hr?
a. 25
b. 0.25
c. 75
d. 0.75
I. Alpha
II. Beta
III. Muscarinic
a. I & II
b. I, II & III
c. II & III
d. I & III
30. Which of the following is TRUE regarding the effects of adrenergic agonists on peristalsis?
a. No effect
b. Decrease in peristalsis
d. Increase in peristalsis
a. II
b. I, II & III
c. II & III
d. I
32. Most of the drugs used in the treatment of Alzheimer’s disease are designed to produce ____________ effects.
a. Serotoninergic
b. Sympathetic
c. Cholinergic
d. Dopaminergic
a. Beta-2
b. Alpha-1
c. Beta-1
d. Alpha-2
34. Which of the following drugs should a patient avoid if he has previously experienced an allergic type of reaction to aspirin?
I. Naproxen
II. Paracetamol
III. Ketoprofen
a. I & III
b. I & II
c. I, II & III
d. II & III
35. Which of the following can reverse the action of lead and other heavy metals?
a. Succimer
b. Atropine
c. Flumazenil
d. Naloxone
36. Which of the following agents used in the treatment of diarrhea is/are opioid derivative/s?
I. Loperamide
II. Attapulgite
III. Diphenoxylate
a. I
b. I & II
c. I & III
d. I, II & III
37. The following are signs and symptoms of Organophosphate poisoning EXCEPT:
a. Diarrhea
b. Tachycardia
c. Miosis
d. Salivation
a. Dryness of mouth
b. Dilation of pupils
d. Inhibition of sweating
40. Which of the following can increase the risk of bleeding due to Warfarin in relation to its PK profile?
a. I & IV
b. II & IV
c. I & III
d. II & III
41. Which of the following drugs can INCREASE the risk of bleeding when combined with Warfarin?
I. Anti-thyroid agents
II. Anti-platelets
III. Anti-thrombotics
a. I, II & III
b. I & III
c. I & II
d. II & III
42. The following would require the need to review the dose, or stop administration of Warfarin EXCEPT:
a. Diuretic
b. Tocolytic
c. Anti-diabetic
d. Anti-arrhythmic
44. Which of the following is also known as the growth hormone-inhibiting hormone? It’s therapeutic use is targeted on blocking
a. Simvastatin
b. Somatostatin
c. Gonadotropin
d. Somatropin
a. Leukotriene modifiers
b. Inhaled corticosteroids
c. Beta agonists
47. Which of the following anti-hypertensives does not act at autonomic receptors?
a. Terazosin
b. Carvedilol
c. Clonidine
d. Hydralazine
48. Sulfonylureas are the primary mode of therapy in the treatment of ____________.
a. Hypoglycemia
b. Hyperglycemia
d. Hepatotoxicity
50. Which of the following is a synthetic analogue of the human amylin that reduces post-prandial glucagon secretion?
a. Metformin
b. Sitagliptin
c. Pramlintide
d. Exenatide
a. Insulin Lispro
b. Insulin Glargine
c. Insulin Glulisine
d. NPH Insulin
52. Which of the following ingredients of a cough and cold preparation is classified as a decongestant?
a. Guaifenesin
b. Phenylpropanolamine
c. Chlorpheniramine
d. Dextromethorphan
53. Drugs commonly known as Setrons are used as:
a. Muscle relaxants
b. Anti-emetics
c. Ant-parkinsonism
d. Anti-neutropenics
I. Anti-viral
II. Anti-bacterial
III. Anti-helminthic
a. II
b. III
c. I & II
d. I, II & III
a. Aztreonam
b. Clavulanic Acid
c. Sulbactam
d. Tazobactam
A patient is treated at the Emergency Room for an infection. She has an allergy to Penicillin that was documented in her medical
chart.
56. If an antimicrobial is being considered for this patient, which of the following may cause cross-sensitivity?
a. Azithromycin
b. Clindamycin
c. Levofloxacin
d. Piperacillin-Tazobactam
57. If the patient was inadvertently given Penicillin inspite of the documented allergy, which of the following BEST describes the
incident?
a. 1st
b. 4th
c. 2nd
d. 3rd
59. Which of the following is a known adverse effect associated with the use of Chloramphenicol?
b. Alopecia
c. Phototoxicity
d. Aplastic anemia
60. Which of the following is the adverse effect associated with Streptomycin?
a. Peripheral neuritis
b. Ototoxicity
c. Optic neuritis
d. Hepatitis
61. Which of the following drugs is primarily used for the treatment of severe infections caused by gram negative bacteria?
a. Gentamicin
b. Vancomycin
c. Doxycycline
d. Cefalexin
62. Arrange the following route of toxin delivery in order, from MOST effective to LEAST effective:
I. Oral
II. Intravenous
III. Subcutaneous
IV. Inhalation
V. Dermal
63. Poisons may enter human body through the following routes of exposure:
I. Orally by ingestion
II. By inhalation
a. I & II
b. II & III
c. I & III
d. I, II & III
64. Which of the following is depleted when there is Paracetamol overdose consequently causing its toxicity?
a. S-adenosylmethionine
b. N-acetyl-p-benzoquinoneimine
c. Glutathione
d. Acetyl CoA
65. Which of the following can be administered to the patient for Acetaminophen poisoning?
a. N-acetylcysteine
b. Dimercaprol
c. Succimer
d. Pralidoxime
a. Vitamin K
b. Vitamin C
c. Vitamin B12
d. Vitamin B6
67. Which of the following is the main physical hazard when administering drugs with vesicant properties?
a. Hypothermia
b. Air embolism
c. Extravasation
d. Thrombosis
69. Which of the following statements are TRUE regarding the similarities of Phenytoin and Phenobarbital?
a. I & II
b. II & III
c. I & III
d. I, II & III
70. Which of the following would be the expected interaction between vasopressors and the beta blockers relative to a patient’s
blood pressure?
a. Synergism
b. Potentiation
c. Antagonism
d. Additive
71. Compute for the Volume of Distribution of the drug in L if the patient received a single intravenous dose of 200mg of a drug
a. 20L
b. 0.5L
c. 500L
d. 0.2L
a. Lidocaine
b. Amiodarone
c. Norepinephrine
d. Desmopressin
73. Which of the following neurotransmitters will be increased by Rivastigmine in the central nervous system synapses?
a. Dopamine
b. Acetylcholine
c. Epinephrine
d. Serotonin
b. Anti-arrhythmia
c. Anti-convulsant
d. Anti-cancer
75. Which of the following is a synthetic analogue of human glucagon-like polypeptide-1 that increases insulin secretion and
a. Sitagliptin
b. Empagliflozin
c. Exenatide
d. Pramlintide
a. Bleomycin
b. Amifostine
c. Doxorubicin
d. Cisplatin
77. All of the following statements regarding drug transport are true EXCEPT:
a. High molecular weight drugs diffuse across cell membrane more easily than low molecular weight drugs.
c. Lipophilic drugs cross cell membranes more easily than hydrophilic drugs.
78. Which of the following pairings of an unwanted effect and the causative drug are TRUE?
a. I & III
b. II & III
c. I
d. I, II & III
a. Ibuprofen
b. Piroxicam
c. Naproxen
d. Sulindac
80. Which of the following will enhance the excretion of an alkaline poison in the urine?
a. Probenecid
b. Urinary Acidifier
c. Urinary Alkalinizer
d. Inulin
a. Terazosin
b. Carvedilol
c. Clonidine
d. Hydralazine
b. If 1 mg of drug A produces the same response as 10mg of Drug B, Drug A is more effective than Drug B.
d. If 1 mg of Drug A produces the same response as 10mg of Drug B, Drug A is more potent than Drug B.
a. I & IV
b. II, III, IV
c. II & III
84. Which of the following equations is used to compute for the patient’s creatinine clearance?
a. Michaelis-Menten Equation
c. Harris-Benedict Equation
d. Henderson-Hasselbalch Equation
85. What is the main difference between 2nd generation and 1st generation H1 receptor antagonists?
a. Class I
b. Class II
c. Class III
d. Class IV
87. Based on the figure below, which of the following new drugs would be the most potent?
a. B
b. C
c. D
d. A
88. Which of the following statements are TRUE regarding eicosanoids?
a. I & II
b. II & III
c. I & II
d. I, II & III
89. Which of the following is an ergot derivative used for the treatment of idiopathic parkinsonism?
a. Bromocriptine
b. Morphine
c. Aspirin
d. Ipratropium
90. Which of the following is useful in treating ascites and pulmonary edema? The principal site of action is on the thick
a. Hydrochlorothiazide
b. Acetazolamide
c. Spirinolactone
d. Furosemide
a. Nevirapine
b. Terbinafine
c. Lamivudine
d. Tenofovir
92. In the management of a poisoned patient, what is the rationale for administering activated charcoal?
a. Chelates the poison to form more water-soluble complexes for faster excretion
c. Counteracts the toxic effects of the poison by producing an opposing pharmacological effect
a. Pernicious Anemia
b. Megaloblastic Anemia
d. Aplastic Anemia
94. Which of the following monoclonal antibody is a tumor necrosis factor-alpha blocker?
a. Omalizumab
b. Infliximab
c. Vedolizumab
d. Reslizumab
95. Which of the following drugs are uric acid synthesis inhibitors?
I. Lesinurad
II. Allopurinol
III. Febuxostat
IV. Rasburicase
a. I & IV
b. II
c. II & IV
d. II & III
a. spasmolytic
b. cardiac drug
c. anti-sialogogue
d. anti-microbial
a. Class IV
b. Class III
c. Class II
d. Class I
a. Hyperglycemia
b. Diarrhea
c. Asthma
d. Neuropathy
99. Which of the following agents has an active metabolite that is capable of neprilysin inhibition?
a. Sacubitril
b. Aliskiren
c. Ticagrelor
d. Nesiritide
a. Enoxaparin
b. Rivaroxaban
c. Vorapaxar
d. Fondaparinux
a. Parkinson’s Disease
b. Alzheimer’s Disease
c. Myasthenia Gravis
d. Depression