PCOL Flashcards
Mechanism of action of local anesthetics.
A. Block sodium channel thereby stopping
axonal conduction
B. Block alpha and beta receptor
C. Block neuronal firing by decreasing Ach
in the neuromuscular junction
D. Inhibition of acetyl cholinesterase
enzyme
E. Inhibition of enzyme responsible for pain response
A. Block sodium channel thereby stopping
axonal conduction
The following are factors that affect the
absorption of drug from the gastrointestinal (GI) track except:
A. Surface area of absorption
B. Blood flow to the site of absorption
C. Physical state of the drug
D. Concentration of the drug at the site of absorption
E. Protein binding
E. Protein binding
Continued stimulation of cells with agonists generally results in which of the following?
A. Desensitization
B. Up-regulation
C. Down-regulation
Desensitization
Down-regulation
Drug that lacks intrinsic efficacy but retains affinity and competes with the agonist for the binding sites of the receptor.
A. Competitive antagonist
B. Full agonist
C. Non-competitive antagonist
D. Partial antagonist
E. Partial agonist
A. Competitive antagonist
This type of drug produce its effect by binding a site on the receptor distinct from that of the primary agonist and thereby changing the affinity of the receptor for the agonist.
A. Competitive antagonist
B. Full agonist
C. Non-competitive antagonist
D. Partial antagonist
E. Partial agonist
C. Non-competitive antagonist
In this type of study, participants are blinded to treatment assignment, investigators are not.
A. Double blind study
B. Single blind study
C. Masking
D. Open-label
E. Un-blinded study
B. Single blind study
The neurotransmitter of all preganglionic autonomic fibers, and all postganglionic parasympathetic fibers:
A. Norepinephrine
B. Noradrenaline
C. Acetylcholine
D. A and B
E. A and C
C. Acetylcholine
The release of ach and other neurotransmitters by exocytosis is inhibited by:
A. Acetylcholinesterase
B. Botulinum toxin
C. Reserpine
D. Metyrosine
E. Guanethidine
B. Botulinum toxin
All of the following are enzymes involved in the biosynthesis of epinephrine from tyrosine EXCEPT:
A. Tyrosine hydroxylase
B. Aromatic L amino acid decarboxylase
C. Dopamine Beta-hydroxylase
D. Phenyl ethanolamine-N-Methyl transferase
E. Monoamine oxidase
E. Monoamine oxidase
Rate limiting enzyme in the synthesis of catecholamines:
A. Tyrosine hydroxylase
B. Aromatic L-amino acid decarboxylase
C. Dopamine beta-hydroxylase
D. Phenyl ethanolamine-N-Methyl transferase
E. COMT
A. Tyrosine hydroxylase
All of the following are effects of activating beta 2 receptor, EXCEPT:
A. Bronchoconstriction
B. Uterine Relaxation
C. Glycogenolysis
D. Gluconeogenesis
E. Bronchodilation
A. Bronchoconstriction
All of the following are effects of activating alpha 1 receptor EXCEPT:
A. Vascular smooth muscle relaxation
B. Intestinal smooth muscle relaxation
C. Increase contractive force of the heart
D. Glycogenolysis in the liver
E. Vascular smooth muscle constriction
A. Vascular smooth muscle relaxation
Which of the following is a pharmacological effect of muscarinic stimulation in the cardiovascular system?
A. Vasoconstriction
B. Decrease in cardiac rate
C. Positive chronotropic effect
D. Positive dromotropic effect
E. Positive inotropic effect
B. Decrease in cardiac rate
All of the following are naturally occurring
chromonematic Alkaid, EXCEPT:
A. Pilocarpine
B. Muscarine
C. Acetylcholine
D. Arecoline
E. None of these
C. Acetylcholine
Which of the following is/are effects of cholinomimetic drugs?
I. Stimulation of GI smooth muscle
II. Stimulation of secretion of exocrine gland
III. Bronchoconstriction
IV. Tachycardia
A. I and II
B. II and III
C. I, II and III
D. I and IV
E. I, II, III and IV
C. I, II and III
Major contraindication to the use of muscarinic agonist are the following EXCEPT:
A. Asthma
B. Hypothyroidism
C. Coronary insufficiency
D. Acid-peptic disease
E. Hypertension
E. Hypertension
Used in the treatment of glaucoma where it is instilled into the eye usually as a 0.5-4% solution.
A. Epinephrine
B. Eye-Mo®
C. Pilocarpine
D. Bethanecol
E. Atropine
C. Pilocarpine
Most effective prophylactic agent for short (4-6 hours) exposure to severe motion, also available as transdermal patch.
A. Atropine
B. Scopolamine
C. Ipratropium
D. Tiotropium
E. Varenicline
B. Scopolamine
Which of the following drugs is/are classified an acetylcholinesterase inhibitor?
I. Pilocarpine
II. Edrophonium
III. Tacrine
IV. Atropine
A. I only
B. I and II
C. II and III
D. I, II and III
E. IV only
C. II and III
Which of the following is not an effect of anti-cholinesterase agents?
A. Stimulation of muscarinic receptor responses at autonomic effector organs
B. Stimulation, followed by depression or paralysis of all autonomic ganglia and skeletal muscle
C. Stimulation, with occasional subsequent depression of cholinergic receptor sites in the CNS
D. All of these
E. None of these
E. None of these
Intoxication with an organophosphorus anticholinesterase agent can be treated with:
A. Atropine
B. Pralidoxime
C. Malathion
D. A and B
E. B and C
D. A and B
This agent is used in the diagnosis of myasthenia gravis
A. Edrophonium
B. Atropine
C. Neostigmine
D. Pralidoxime
E. Acetylcholine
A. Edrophonium
All are standard anticholinesterase drugs used in the symptomatic treatment of myasthenia gravis, EXCEPT:
A. Pyridostigmine
B. Neostigmine
C. Atropine
D. Ambenonium
E. Edrophonium
C. Atropine
Mechanism of action of indirect acting sympathomimetics drugs:
A. Agents act directly on one or more of the adrenergic receptors thereby producing an effect
B. Increase the availability of norepinephrine (NE) or epinephrine (Epi) to stimulate adrenergic receptors
C. Releasing or displacing NE from sympathetic nerve varicosities
D. A and B
E. B and C
E. B and C
Metabolic precursor of NE and EPI and is also a neurotransmitter particularly important in the regulation movement.
A. Dopamine
B. Serotonin
C. Oxytocin
D. Norepinephrine
E. Noradrenaline
A. Dopamine
These drugs play a major role only in the treatment of bronchoconstriction in patients with asthma (reversible airway obstruction) or chorionic obstructive pulmonary disease (COPD).
A. Beta 1 adrenergic agonist
B. Beta 2 adrenergic agonist
C. Beta 1 adrenergic antagonist
D. Beta 2 adrenergic antagonist
E. Non-selective beta agonist
B. Beta 2 adrenergic agonist
Potent, non-selective beta receptor agonist with very low affinity for alpha receptors
A. Ipratropium
B. Terbutaline
C. Isoproterenol
D. Prazosin
E. Phenylephrine
C. Isoproterenol
This sympathomimetic drug is indicated for the short-term treatment of cardiac decompensation post cardiac surgery or in patients with congestive heart failure or acute myocardial infarction.
A. Dobutamine
B. Isoproterenol
C. Metaproterenol
D. Albuterol
E. Isoetharine
A. Dobutamine
Selective beta 2 agonist originally developed as a uterine relaxant.
A. Terbutaline
B. Ritodrine
C. Oxytocin
D. Prazosin
E. Salmeterol
B. Ritodrine
Life-threatening condition characterized by inadequate perfusion of tissues, hypotension and ultimately failure of organ systems.
A. Coma
B. Shock
C. Arrhythmia
D. Heart Failure
E. Kidney Failure
B. Shock
Structurally related to amphetamine, this drug is a mild CNS stimulant with more prominent effects on mental than on motor activities. This drug is also effective in the treatment of narcolepsy and ADHD.
A. Methamphetamine
B. Ephedrine
C. Clonidine
D. Methylphenidate
E. Phenobarbital
D. Methylphenidate
Classified as alpha 2 selective antagonist.
A. Phenoxybenzamine
B. Prazosin
C. Yohimbine
D. Nadolol
E. Metoprolol
C. Yohimbine
Classified as beta 1 selective antagonist.
A. Phenoxybenzamine
B. Prazosin
C. Yohimbine
D. Nadolol
E. Metoprolol
E. Metoprolol
Used in the treatment of pheochromocytoma, tumor of the adrenal medulla and sympathetic neurons that secrete enormous quantities of catecholamines.
A. Phenoxybenzamine
B. Epinephrine
C. Metoprolol
D. Dopamine
E. Isoxuprine
A. Phenoxybenzamine
Which of the following is NOT correct?
A. Alpha agonist cause miosis
B. Alpha agonist cause vasoconstriction
C. Beta antagonist decrease the formation of aqueous humor
D. Beta 2 agonist cause bronchodilation
E. Beta 3 agonist cause lipolysis
A. Alpha agonist cause miosis
Beta 2 receptor stimulation includes all of the following effects EXCEPT:
A. Stimulation of renin secretion
B. Fall of potassium concentration is plasma
C. Relaxation of bladder uterus
D. Uterine muscle contraction
E. Skeletal muscle relaxation
D. Uterine muscle contraction
Which of the following effects is associated with beta 3-receptor stimulation?
A. Lipolysis
B. Decrease in platelet aggregation
C. Bronchodilation
D. Tachycardia
E. Pilomotor smooth muscle contraction
A. Lipolysis
Which of the following hypnotic drug is benzodiazepine derivative?
A. Zolpidem
B. Flurazepam
C. Secobarbital
D. Ramelteon
E. Buspirone
B. Flurazepam
Which of the following hypnotic drug increase the activity of hepatic drug-metabolizing enzyme systems?
A. Phenobarbital
B. Zolpidem
C. Flurazepam
D. Secobarbital
E. Ramelteon
A. Phenobarbital
Which of the following is the mechanism of Barbiturates action?
A. Increasing the duration of the GABA gated Cl-channel openings
B. Directly activating the chloride channel
C. Increasing the frequency of Cl-channel openings events
D. Antagonist at benzodiazepine bindings sites on the GABA receptor
E. Partial agonist at 5-HT receptor but also affinity for D2 receptor.
A. Increasing the duration of the GABA gated Cl-channel openings
The usual cause of adverse effect/death
due to overdose of hypnotics due to:
A. Depression of the CNS
B. Heart attack
C. Hypothermia
D. Cerebral edema
E. Status epilepticus
A. Depression of the CNS
Which of the following antiseizure drugs produces a voltage-dependent inactivation of sodium channels?
I. Phenytoin
II. Carbamazepine
III. Vigabatrin
IV. Gabapentin
A. I only
B. I and II
C. II and III
D. II and IV
E. IV only
B. I and II
Mechanism of action of phenytoin:
A. Block high-frequency firing of neurons through action on voltage-gated (VG) Na+ channel
B. It binds to an allosteric regulatory site on the GABA-BZ receptor and prolongs the opening of the Cl-channel
C. It effects on the Ca2+ currents, reducing the low-threshold (T-type) current
D. It inhibits GABA-transaminase, which catalyzes the breakdown of GABA
E. Decreases the excitatory transmission by acting on the VG Ca2+ channels presynaptically
A. Block high-frequency firing of neurons through action on voltage-gated (VG) Na+ channel
The pathophysiologic basis for anti-parkinsonism therapy is:
A. The loss of dopaminergic neurons
B. The loss of some cholinergic neurons
C. The loss of the GABAergic cells
D. The loss of glutaminergic neurons
E. Abnormal firing of neurons from the CNS
A. The loss of dopaminergic neurons
Which of the following drugs is used in the treatment of parkinsonian disorders?
A. Phenytoin
B. Selegeline
C. Haloperidol
D. Fluoxetine
E. Aspirin
B. Selegeline
The mechanism of action of carbidopa is:
A. Stimulating the synthesis release, or reuptake of dopamine
B. Inhibition of DOPA decarboxylase enzyme
C. Stimulating dopamine receptors
D. Inhibition of COMT
E. Monoamine oxidase inhibitor
B. Inhibition of DOPA decarboxylase enzyme
Which of the following statements is correct?
A. MAO-A metabolizes dopamine; MAO-B metabolizes serotonin
B. MAO-A metabolizes norepinephrine and dopamine; MAO-B metabolizes serotonin
C. MAO-A metabolizes norepinephrine and serotonin; MAO-B metabolizes dopamine
D. MAO-A metabolizes dopamine; MAO-B metabolizes norepinephrine and serotonin
E. MAO-A metabolizes dopamine; MAO-B metabolizes epinephrine
C. MAO-A metabolizes norepinephrine and serotonin; MAO-B metabolizes dopamine
A catechol O-methyl transferase inhibitor, which prolongs the action of levodopa by diminishing its peripheral metabolism:
A. Carbidopa
B. Clozapine
C. Tolcapone
D. Rasagiline
E. Selegiline
C. Tolcapone
Mu receptors are associated with:
A. Supraspinal and spinal analgesia, sedation, respiratory depression and slowed GI transit
B. Spinal analgesia, mydriasis sedation physical dependence
C. Dysphoria, hallucinations, respiratory and vasomotor stimulation
D. Analgesia, euphoria, respiratory stimulation, physical dependence
E. CNS stimulation and respiratory stimulation
A. Supraspinal and spinal analgesia, sedation, respiratory depression and slowed GI transit
Which of the following opioid analgesics is a strong mu receptor agonist?
A. Morphine
B. Pentazocine
C. Buprenorphine
D. Naloxone
E. Propoxyphene
A. Morphine
Which of the following agents is a full antagonist of opioid receptors?
A. Meperidine
B. Buprenorphine
C. Naloxone
D. Butorphanol
E. Morphine
C. Naloxone
The diagnostic triad of opioid overdosage is:
A. Mydriasis, coma and hyperventilation
B. Coma, depressed respiration and miosis
C. Mydriasis, chills and abdominal cramps
D. Miosis, tremor and vomiting
E. Mydriasis, diarrhea, increase urination
B. Coma, depressed respiration and miosis
Which of the following non-narcotic agents is salicylic acid derivative?
A. Phenylbutazone
B. Ketamine
C. Aspirin
D. Tramadol
E. Diclofenac
C. Aspirin
Correct statements concerning aspirin include all of the following except:
A. Irreversibly inhibits platelet COX
B. Main adverse effects at antithrombotic doses are gastric upset (intolerance) and gastric and duodenal ulcers
C. It inhibits platelet aggregation
D. Safe to use in patients with hemophilia
E. Epidemiologic studies suggest that long term use of aspirin at low dosage is associated with a lower incidence of colon cancer
D. Safe to use in patients with hemophilia
A drug that inhibit HMG-CoA reductase. It also reduces cholesterol synthesis and up regulate low density lipoprotein (LDL) receptors on hepatocytes.
A. Fenofibrates
B. Colestipol
C. Ezetimibe
D. Atorvastatin
E. Niacin
D. Atorvastatin
A vasodilator that also inhibits plates function by inhibiting adenosine uptake and cGMP phosphodiesterase activity.
A. Dipyridamole
B. Abciximab
C. Clostazol
D. Anistreplase
E. Streptokinase
A. Dipyridamole
The mathematical product of peripheral vascular resistance (PVR) and cardiac output (CO).
A. Hypertension
B. Blood Pressure
C. Hypotension
D. Vascular pressure
E. Afterload
B. Blood Pressure
Recommendation on dietary approaches to stop hypertension (DASH).
A. High intake of fruits
B. Low fats dairy products along with reduced content of dietary cholesterol saturated fat and total fat
C. The diet is rich on potassium and calcium and low in sodium
D. High intake of vegetables
E. All of these
E. All of these
Recommend Blood Pressure Targets for patient with heart failure
A. <150 / <90
B. <140 / <90
C. <140 / <80
D. <160 / <90
E. <130 / <80
E. <130 / <80
Increase the excretion of Na+, CI+ and H2O by inhibiting Na+ /Cl+ ion exchange in the early part of the distal tubule:
A. Thiazide diuretics
B. Loop diuretic
C. Potassium Sparring diuretics
D. Aldosterone Antagonists
E. Osmotic diuretics
A. Thiazide diuretics
Drug that antagonize angiotensin II at the AT1 receptor subtype, which decrease systemic vascular resistance.
A. Furosemide
B. Amiloride
C. Metoprolol
D. Captopril
E. Losartan
E. Losartan
Reduce both resting and exercise heart rate, cardiac output and both systolic and diastolic blood pressure
A. Furosemide
B. Amiloride
C. Metoprolol
D. Captopril
E. Losartan
C. Metoprolol
Block the conversion of angiotensin I to angiotensin II by interfering with angiotensin converting enzyme (ACE) activity
A. Furosemide
B. Amiloride
C. Metoprolol
D. Captopril
E. Losartan
D. Captopril
A condition of chronic excess total body iron caused either by an inherited abnormality of iron Absorption or by frequent transfusion to treat certain types of hemolytic disorders:
A. Hemochromatosis
B. Megaloblastic anemia
C. Microcytic anemia
D. Neutropenia
E. Pernicious anemia
A. Hemochromatosis
A Deficiency in serum hemoglobin and erythrocytes in which the erythrocytes are abnormally large. Results from either folate or vitamin B12 deficiency
A. Hemochromatosis
B. Megaloblastic anemia
C. Microcytic anemia
D. Neutropenia
E. Pernicious anemia
B. Megaloblastic anemia
A deficiency in serum hemoglobin and erythrocytes in which the erythrocytes are abnormally small. Often caused by iron deficiency.
A. Hemochromatosis
B. Megaloblastic anemia
C. Microcytic anemia
D. Neutropenia
E. Pernicious anemia
C. Microcytic anemia
An abnormally low number of neutrophils in the blood; patients with this condition are susceptible to serious infection
A. Hemochromatosis
B. Megaloblastic anemia
C. Microcytic anemia
D. Neutropenia
E. Pernicious anemia
D. Neutropenia
A form of megaloblastic anemia resulting from deficiency of intrinsic factor, a protein produced by gastric mucosal cell and required for intestinal absorption of vitamin B12
A. Hemochromatosis
B. Megaloblastic anemia
C. Microcytic anemia
D. Neutropenia
E. Pernicious anemia
E. Pernicious anemia
Required for biosynthesis of heme and heme-containing proteins, including hemoglobin and myoglobin
A. Deferoxamine
B. Vitamin B12
C. Folic Acid
D. Ferrous sulfate
E. Filgrastim
D. Ferrous sulfate
Stimulates G-CSF receptors expressed on mature neutrophils and their progenitors for the treatment of neutropenia:
A. Deferoxamine
B. Vitamin B12
C. Folic acid
D. Ferrous sulfate
E. Filgrastim
E. Filgrastim
An endogenous anticlotting protein that irreversibly inactivates thrombin and factor Xa. Its enzymatic action is markedly accelerated by the heparins
A. Antithrombin III
B. Glycoprotein IIb/IIIa
C. Clotting cascade
D. Prothrombin
E. A and B
A. Antithrombin III
A protein complex on the surface of platelets. When activated, it aggregates platelets primarily by binding to fibrin.
A. Antithrombin III
B. Glycoprotein IIb/IIIa
C. Clotting cascade
D. Prothrombin
E. A and C
B. Glycoprotein IIb/IIIa
Laboratory test used to monitor the anticoagulant effect of unfractionated heparin and direct thrombin inhibitors; prolonged when drug effect is adequate
A. Activated partial thromboplastin time (aptt) test
B. Clotting cascade
C. Prothrombin time (PT) test
D. Platelet test
E. Coagulase test
A. Activated partial thromboplastin time (aptt) test
Laboratory test used to monitor the anticoagulant effect of warfarin; prolonged when drug effect is adequate
A. Activated partial thromboplastin time (apt) test
B. Clotting cascade
C. Prothrombin time (PT) test
D. Platelet test
E. Coagulase test
C. Prothrombin time (PT) test
Which of the following are classified as thrombolytic agents?
I. Streptokinase
II. Warfarin
III. T-PA derivatives
IV. Heparins
A. I and II
B. II and III
C. I and III
D. II and IV
E. IV only
C. I and III
What is the bactericidal concentration of ethanol and isopropanol by volume in water?
A. 60 – 90%
B. 30 – 50%
C. 70 – 99%
D. 80 – 100%
E. 10 – 20%
A. 60 – 90%
It is a destruction of marked reduction in number of activity of microorganisms.
A. Antisepsis
B. Decontamination
C. Disinfection
D. Sterilization
E. Pasteurization
B. Decontamination
It contains 2% Iodine and 2.4% NaI in alcohol and is the most active antiseptic for intact skin
A. Iodophors
B. Povidone iodine
C. Tincture of Iodine USP
D. Iodine solution
E. Both A and B
C. Tincture of Iodine USP
A phenolic disinfectant that cause cerebral edema and convulsions in premature infants.
A. O-phenyl phenol
B. P-Amylphenol
C. O-benzyl-P-Chlorophenol
D. Heptachlorophene
E. Hexachlorophene
E. Hexachlorophene
The following has an excellent efficacy on infection caused by Pneumocystis jiroveci pneumonia except:
A. Penicillin
B. Dapsone
C. Atrovaquone
D. Trimetoprim-sulfamethoxazole
E. None of these
A. Penicillin
First line drug in treating early stage of infection caused by West African trypanosomiasis
A. Pentamidine
B. Melarsoprol
C. Metronidazole
D. Iodoquinol
E. Tetracycline
A. Pentamidine
It inhibits topoisomerase II and has a side effect of alopecia and myelosuppression
A. Irinotecan
B. Etoposide
C. Paclitaxel
D. Vinblastine
E. Vincristine
B. Etoposide
The FDA approved a novel, oral and highly selective small molecule inhibitor of BRAFV600E last August 2011 and has a highly promising activity in metastatic melanoma. What drug is this?
A. Lomustine
B. Camustine
C. Cyclophosphamide
D. Vemurafenib
E. Etoposide
D. Vemurafenib
It is an immunosuppressant macrolide antibiotic produced by Steptomyces tsukabaensis
A. Cyclosporine
B. Tacrolimus
C. Temsirolimus
D. Cycloserine
E. Sirolimus
B. Tacrolimus
What class of Gastrointestinal drugs are most effective agents for the treatment of non-erosive and erosive reflux disease and extra-esophageal manifestation of reflux disease?
A. NSAID
B. H2 receptor antagonist
C. Proton Pump inhibitor
D. Prostaglandin analogs
E. H1 receptor antagonist
C. Proton Pump inhibitor
The following are common preparation of natural plant products which are bulk forming laxatives except
A. Psyllium
B. Methylcellulose
C. Polycarbophil
D. A and B
E. None of these
C. Polycarbophil
It is the most commonly used osmotic laxative and should not be used for prolonged periods for patient with renal insufficiency due to the risk of hypermagnesemia
A. Magnesium hydroxide
B. Milk of Magnesia
C. Furosemide
D. A and B
E. Mannitol
D. A and B
It is effective in reducing nocturnal acid but is less effective against stimulated secretion
A. H2 receptor antagonist
B. PPI
C. Sucralfate
D. Laxative
E. Diuretic
A. H2 receptor antagonist
Ondansetron and Granisetron block which receptor site?
A. 5HT3
B. 5HT1A
C. 5HT1B
D. 5HT1C
E. 5HT4
A. 5HT3
These are example of amides:
I. Lidocaine
II. Bupivacaine
III. Cocaine
IV. Prilocaine
A. I and II
B. I, II and III
C. I, II and IV
D. II, III and IV
E. I, II, III and IV
C. I, II and IV
High Plasma concentration of local anesthetics result from rapid absorption, thus causing:
I. Sedation
II. Light headedness
III. Auditory disturbances
IV. Restlessness
A. I and II
B. I, II and III
C. I, II and IV
D. I and IV
E. I, II, III and IV
E. I, II, III and IV
Selective Serotonin-Norepinephrine Reuptake Inhibitor include:
I. Venlafaxine
II. Sertraline
III. Duloxetine
IV. Citalopram
A. I only
B. I, II and III
C. I, II and IV
D. I and III
E. II and III
D. I and III
Which pair is mismatch?
I. Butyrophenone – Haloperidol
II. Atypical antipsychotics – Clozapine
III. Thioxanthene – Thiothixene
IV. Phenothiazine – Chlorpromazine
A. I only
B. II only
C. III only
D. IV only
E. None of these
E. None of these
Which of the following is NOT true about opioids?
I. Opioid analgesics may prolong labor
II. Opioids contract biliary smooth muscle
III. Opioid analgesics stimulates release of ADH, Prolactin and Somatropin
IV. Opioids causes mydriasis
A. I, II, III and IV
B. IV only
C. III only
D. I only
E. II only
B. IV only
Which of the following is mismatch?
I. Factor I – Fibrinogen
II. Factor XII – Fibrin-Stabilizing factor
III. Factor XI – Prothrombin
IV. Factor X – Stuart power factor
A. III only
B. IV only
C. I and II
D. II, III and IV
E. I, II, III and IV
A. III only
The deficiency of factor IX can cause hemophilia B and Christmas Disease. Hemophilia A is also known as Christmas Disease.
A. Only the 1st statement is correct
B. Only the 2nd statement is correct
C. Both statements are correct
D. Both statements are wrong
A. Only the 1st statement is correct
The following are non-selective COX inhibitor EXCEPT:
I. Diclofenac
II. Celecoxib
III. Meloxicam
IV. Ibuprofen
A. I and II
B. II and III
C. III and IV
D. I and IV
E. IV only
B. II and III
It is a peptide antibiotic and is considered as a non-biologic DMARD
A. Cycloserine
B. Cyclosporine
C. Chloroquine
D. Abatacept
E. Azathioprine
B. Cyclosporine
It is the active metabolite of phenacetin
I. Acetaminophen
II. N-acetyl-p-aminophenol
III. N-acetylcysteine
IV. ASA
A. IV only
B. I only
C. I and II
D. III only
E. I, II, III and IV
C. I and II
It is the most common form of hyperthyroidism
A. Myxedema coma
B. Subacute thyroiditis
C. Ophthalmopathy
D. Grave’s disease
E. None of these
D. Grave’s disease
This is the sudden acute exacerbation of all of the symptoms of thyrotoxicosis presenting as a life-threatening syndrome
I. Myxedema coma
II. Grave’s disease
III. Thyroid Storm
IV. Thyrotoxic crisis
A. I only
B. II only
C. III only
D. I and II
E. III and IV
E. III and IV
A syndrome of thyroid enlargement without excessive thyroid hormone production
A. Non-toxic goiter
B. Thyroid neoplasms
C. Neonatal Grave’s Disease
D. Myxedema coma
E. Thyroiditis
A. Non-toxic goiter
What is the route of administration of methyltestosterone?
I. IM
II. IV
III. Oral
IV. Transdermal
A. I and II
B. III and IV
C. I only
D. III only
E. None of these
D. III only
It is a chemotherapeutic drug which is a folic acid analog that binds with high affinity to the active catalytic site of dihydrofolate reductase:
A. Cisplatin
B. Dacarbazine
C. Methotrexate
D. Vincristine
E. Gemcitabine
C. Methotrexate
A catechol-o-methyltransferase inhibitor
A. Selegiline
B. Entacapone
C. Pergolide
D. Ropinirole
E. Rotigotine
B. Entacapone
The combination of these are the most effective for H. pylori associated ulcers:
I. Antibiotic
II. PPI
III. H2 receptor blocker
IV. Prostaglandin analogs
A. Antibiotic and PPI
B. PPI and H2 receptor blocker
C. H2 receptor blocker and prostaglandin analogs
D. Antibiotic and H2 receptor blocker
E. Antibiotic and prostaglandin analog
A. Antibiotic and PPI
It is the most common leukemia in adults.
A. Acute Lymphoblastic Leukemia
B. Acute Myelogenous Leukemia
C. Hodgkin’s Leukemia
D. Non-Hodgkin’s Leukemia
E. None of these
A. Acute Lymphoblastic Leukemia
What type of organ transplant rejection occurs within hours and cannot be stopped with immunosuppressive drug and occurs due to performed antibodies against the donor organs?
A. Acute
B. Accelerated
C. Hyperacute
D. Chronic
E. Superficial
C. Hyperacute
The hallmark of this type of diabetes is selective beta cell destruction and severe or absolute insulin deficiency
A. Type 1
B. Type 2
C. Type 3
D. Type 4
E. All of these
A. Type 1
This is the main form of leukemia in childhood, and it is the most common form of cancer in children
A. Acute Lymphoblastic Leukemia
B. Acute Myelogenous Leukemia
C. Hodgkin’s Leukemia
D. Non-Hodgkin’s Leukemia
E. None of these
A. Acute Lymphoblastic Leukemia
Its generic name is Imiquimod and it is used in the treatment of external genital and perianal warts in adults. Available as 5% cream.
A. Protopic
B. Aldara
C. Elidel
D. Zovirax
E. Denavir
B. Aldara
Podophyllum resin, an alcoholic extract of mandrake root or May apple is used in the treatment of:
A. Condyloma Acuminatum
B. Psoriasis
C. Photophobia
D. Lichen simplex chronicus
E. Cushing’s syndrome
A. Condyloma Acuminatum
A combination of levodopa and MAO-A inhibitors could lead to this condition:
A. Hypertensive Crisis
B. Alopecia
C. Memory Loss
D. Hyperactivity
E. GI bleeding
A. Hypertensive Crisis
This is also known as manic-depressive illness
A. Anxiety
B. Bipolar Disorder
C. Obstructive-compulsive disorder
D. ADHD
E. None of these
B. Bipolar Disorder
This vitamin enhances the extracerebral metabolism of levodopa
A. Vitamin A
B. Vitamin B9
C. Vitamin B6
D. Vitamin E
E. Vitamin D
C. Vitamin B6
PGE1 analog used to treat erectile dysfunction:
A. Alprostadil
B. Misoprostol
C. Dinoprostone
D. Epoprostenol
E. Prostin E2
A. Alprostadil
Which of the following is an example of piperidine type of phenothiazines?
I. Thioridazine
II. Piperacetazine
III. Mesoridazine
IV. Carphenazine
A. I and II
B. III and IV
C. I, II and III
D. II, III and IV
E. I, II, III and IV
C. I, II and III
PGE1 analog used as treatment and prophylaxis of NSAID-included gastric ulcer and is also an abortifacient drug.
A. Alprostadil
B. Misoprostol
C. Dinoprostone
D. Epoprostenol
E. Prostin E2
B. Misoprostol
Drug for the treatment of gout which blocks xanthine oxidase thereby decreasing the production of uric acid:
A. Indomethacin
B. Colchicine
C. Allopurinol
D. Febuxosat
E. C and D
E. C and D
Drug for gout which increase urinary excretion of uric acid (inhibits reabsorption of uric acid in the proximal tubule):
A. Indomethacin
B. Colchicine
C. Allopurinol
D. Febuxosat
E. Probenecid
E. Probenecid