Pharmacology 201-500 Flashcards
Which of the following chemotherapeutic drugs may be used for Lentigo Maligna? A. Actinomycin B. Bleomycin C. Doxorubicin D. Vinblastine E. Cisplatin
A
Which of the following chemotherapeutic drugs may be used for Lung Cancer? A. Procarbazine B. Cytarabine C. Topotecan D. Cisplatin E. Cyclophosphamide
D
Which of the following drugs is an effective prophylactic drug against migraine headache attacks? A. Ondansetron B. Sumatriptan C. Ergotamine D. Methylergonovine E. Propranolol
E
A newly formulated drug with a half life of 6 hours is eliminated via 1st order kinetics, how many hours will the drug be 100% eliminated from the body of a normal person? A. 6 hours B. 12 hours C. 18 hours D. 24 hours E. 36 hours
D
100% elimination will be reached in 4
half lives. (6 x 4=24)
In calculating the loading dose of a drug, which of the following parameters are not necessary? A. Volume of distribution B. Desired Plasma Concentration C. Bioavailability D. Clearance E. None of the Above
D
LD = (Vd x DPC) / Bioavailability
Which of the following is a reversible inhibitor of Xanthine Oxidase used in Chronic Gout? A. Allopurinol B. Colchicine C. Febuxostat D. Mycophenolate Mofetil E. Probenecid
C
Allopurinol is an IRREVERSIBLE Xanthine Oxidase inhibitor, Febuxostat is a REVERSIBLE Xanthine Oxidase inhibitor,
A patient will be undergoing neurosurgery, the neurosurgeon would like to maintain the patient's consciousness while the procedure is on going. What would be the preferred anesthetic of choice? A. Ketamine B. Etomidate C. Midazolam D. Fentanyl
A
Ketamine is capable of Dissociative Anesthesia ( Analgesia, Amnesia and Catatonia with retained consciousness)
A 14 year old child was diagnosed with Schizophrenia, which of the following is the only antipsychotic approved for pediatric patients? A. Clozapine B. Risperidone C. Quetiapine D. Olanzapine E. Thioridazine
B
The following statements are true of Aminoglycosides, EXCEPT:
A. Act by TimeDependent Killing Action
B. As the plasma level is increased above the MIC an increasing proportion of bacteria are killed and at a more rapid rate
C. Has a post-antibiotic eff
A
Among the following Anti-arrhythmics, which of the following has a highest potential for Torsade de pointes? A. Lidocaine B. Propranolol C. Sotalol D. Procainamide E. Verapamil
C
K channel blockers like Sotalol can increase the QT interval thereby increasing the propensity to develop Torsade de Pointes
A patient with CHF was rushed to the ED where you are on-duty, ABG was done revealing Metabolic Acidosis. His wife told you that he had a history of severe allergic reaction to Sulfa drugs, but you need to give the patient a powerful diuretic, Unfortunate
D
Spironolactone and Acetazolamide can aggravate the ongoing acidosis of the patient, the only ones left are loop diuretics, but then Furosemide and Torsemide are both Sulfa containing hence cannot be given to the patient. Ethacrynic acid is most suitabl
To improve the quality of life of patients with on-going treatment for Prostate Adenocarcinoma with Leuprolide, which of the following medications should be added? A. Anastrazole B. Examestane C. Flutamide D. Prednisone E. Morphine
C
Flutamide an Androgen Antagonist is given in adjunct to Leuprolide to lessen the side effects of Leuprolide like Gynecomastia, decreased libido, Apoplexy and hot flushes.(SIMILAR TO PREVIOUS BOARD EXAM CONCEPT/PRINCIPLE)
A 9-year old Filipino child was brought to you in the clinics by her mother due to an observed blank-stare episodes noted by her mother which lasts from a few seconds to a few minutes. Which of the following medications is the most suitable for this patie
A
Valproate is the DOC for Absence Seizures, most especially in our setting here in the Philippines, Ethosuximide is NOT commercially available.
Which of the following Beta Blockers has an Intrinsic Sympathomimetic Activity? A. Carvedilol B. Pindolol C. Nadolol D. Metoprolol E. Timolol
B
Pindolol has ISA, which makes it a B blocker with a partial Alpha agonist action.
Early morning hypoglycemia is a challenge among physicians in treating diabetic patients. When a diabetic patient monitors his Glucose at 3 AM revealing Hypoglycemia with a Hyperglycemic 7 AM CBG, This effect is termed as:
A. Somogyi
B. Waning
C.
A
In a patient with Grave's Disease this drug is given to decrease peripheral conversion of T4 to T3: A. Propranolol B. I 131 C. Methimazole D. PTU E. Lugol's Iodine
A
In a Diabetic patient with impaired renal function which of the following drugs is contraindicated? A. Nateglinide B. Glipizide C. Metformin D. Pioglitazone E. Acarbose
B
Before prescribing 2nd generation Sulfonylureases liver and hepatic function must be checked first because they are contraindicated.
Which of the following Cephalosporins is synergistic with Aminoglycosides? A. Cefazolin B. Cefaclor C. Cefixime D. Cefipime E. Loracarbef
C
3rd gen Cephalosporins have syndergistic effects with Aminoglycosides, 1st and 2nd gen cephalosporines can increase nephrotoxic effects of aminoflycosides.
What class of antihypertensive drugs are also used in BPH? A. Alpha 1A Agonists B. Alpha 1B Agonists C. Alpha 1A Antagonists D. Alpha 1B Antagonists E. Alpha 2 Agonists
C
Alpha 1-A receptor is specifically seen in the Urinary tract most especially the Prostate.Alpha 1A antagonists/Quinazolines include Prazosin Terazosin, and Tamsulosin
Cocaine has which of the following mechanism of action?
A. Promotes Adrenergic Synthesis
B. Inhibits Adrenergic Storage
C. Promotes Adrenergice Release
D. Inhibits Adrenergic Metabolism/Degradation
E. Inhibits Adrenergic Reuptake
E
A condition where there is depletion of needed substrates as a result of continuous activation by a drug and hence decrease in responsiveness, such as in chronic nitroglycerin use, is known as:
A. Tachyphylaxis
B. Idiosyncratic response
C. Tolera
C
Idiosyncratic means unusual drug reponse, infrequently observed in most patients; tolerance on the other hand, refers to decrease in the intensity of response to drug as a consequence of continued administration
Teratogenesis is one of the dreaded complications of improper use of drugs during pregnancy. Of note, lithium, a drug primarily used to treat bipolar disorders, can cause: A. Ebstein's anomaly B. Vaginal clear cell adenocarcinoma C. Phocomelia D.
A
Pralidoxime is an antidote to organophosphate poisoning. Which of the following is not true about this drug?
A. It is a cholinesterase regenerator.
B. It requires to be given 6-8 hours before organophosphatecholinesterase binding occurs.
C. It binds wi
E
Methyldopa is a drug of choice in treating preeclampsia. Its ability to lower blood pressure is based on its action of:
A. Activating alpha-1 adrenergic receptors
B. Inhibiting alpha-1 adrenergic receptors
C. Activating alpha-2 adrenergic recepto
C
Activation of alpha-2 adrenergic receptors by methyldopa metabolites in the brainstem appears to inhibit sympathetic nervous system output and lower blood pressure. This is also the mechanism of action of clonidine. Activation of alpha-1 adrenergic rec
Hydralazine lowers BP by causing arteriolar smooth muscle relaxation. This effect is achieved by its ability to alter metabolism of which ion? A. Sodium B. Potassium C. Magnesium D. Calcium
D
Throbbing headaches in patients taking nitrates are mainly attributed to: A. Chemical toxicity B. Meningeal artery vasodilation C. Reflex tachycardia D. Abrupt lowering of BP
B
Which diuretic is found to have long-term benefits and can reduce mortality in chronic heart failure? A. Thiazide B. Furosemide C. Spironolactone D. Ethacrynic acid
C
Aside from its lipidlowering action, statins are used in coronary artery disease because it can also:
A. Vasodilate stenotic segments of the coronary
B. Stabilize atherosclerotic plaques
C. Inhibits platelet aggregation
D. Decrease myocardial oxygen d
B
Which of the following is considered as a reliever of asthma rather than a controller? A. Montelukast B. Cromolyn C. Omalizumab D. Terbutaline
D
Terbutaline is a beta-2 receptor agonist used as a fast-acting bronchodilator for asthma and is also used in preventing premature labor (tocolysis).
Oral chelation treatment in hemochromatosis can be done by giving: A. Deferoxamine B. Deferasirox C. EDTA D. Penicillamine
B
Therapeutic phlebotomy is the main line of treatment of hemochromatosis, especially the primary type. Should chelation becomes warranted, it can be done via IV (deferoxamine) or oral (Deferasirox).
Aspirin toxicity results in increased respiratory drive that leads to hyperventilation and respiratory alkalosis. Which of these statements is not true about aspirin intoxication?
A. It is achieved when given at a dose of 150 mg/kg.
B. It can manifes
C
Aspirin is not an inhibitor of electrontransport chain (ETC), but an uncoupler. Uncouplers of oxidative phosphorylation in mitochondria inhibit the coupling between the electron transport and phosphorylation reactions and thus inhibit ATP synthesis wit
Tranexamic acid is used to prevent and treat acute bleeding episodes in patients who are at high risk, especially those who have hemophilia and intracranial aneurysms. The mechanism of action of this drug involves:
A. Inhibition of plasminogen activators
A
Plasminogen are converted to plasmin whose function is to lyse the formed fibrin. When it is inhibited, hemostasis is promoted.
Treatment for inflammatory bowel disease: A. Sulfadiazine B. Sulfasalazine C. Sulfamethoxazole D. Sulfatide
B
Sulfasalazine is poorly absorbed in the GIT and therefore it is believed that it has its main action in lumen. It is used to treat IBDs by reducing the synthesis of inflammatory mediators known as eicosanoids and inflammatory cytokines. However, unlike
Remarkable to these drugs is their ability to inhibit cytochrome P450 causing significant interactions with other drugs, except: A. Isoniazid B. Cimetidine C. Erythromycin D. Barbiturates
D
Drugs like quinidine, procainamide and disopyramide are very useful in treatment of: A. Congestive heart failure B. Hypertension C. Thyrotoxicosis D. Status asthmaticus E. Arrhythmia
C
Antifolates sulfamethoxazole and trimethoprim are bactericidal by virtue of their synergistic actions. Nonetheless, resistence can develop via plasmidmediated:
A. Decrease in sensitivity of dihydropteroate synthase to sulfonamides
B. Increase in PABA sy
D
Isoniazid is the most important drug used in TB. It inhibits mycolic acid synthesis and is therefore bactericidal. Possible adverse effects include neuritis, insomnia and seizures. To prevent neurotoxicities, patient should be supplemented with:
A. Fol
B
What is the drug of choice for the cyst carrier state of Entamoeba histolytica? A. Diloxanide furoate B. Metronidazole C. Tinidazole D. Paramomycin
A
Diloxanide furoate is a luminal amoebicide which is hydrolysed in the gut, thus releasing the free diloxanide which acts as an amoebicide. It is given alone in asymptomatic cyst passers. For patients with active amoebic infections, it can be administer
A vinca alkaloid acting primarily in the M phase of cancer cell cycle that is useful in the treatment of acute leukemias, lymphomas and neuroblastoma: A. Paclitaxel B. Vincristine C. Doxorubicin D. Cytarabine
B
This is a mucosal protective drug used as an adjunct treatment of PUD. It binds to injured tissues and forms a protective covering over ulcer beds, resulting in accelerated healing: A. Misoprostol B. Bismuth salicylate C. Calcium carbonate D.
D
Factor/s that influence/s passage of drugs through cell membranes: A. Presence of pores in the membrane B. Amount of protein binding C. Lipid solubility D. pH E. All of the above
E
All are factors that influence passage of drugs through cell membranes. Lipid solubility is the most important limiting factor for permeation of drugs because cells are covered by lipid membranes.
In this clinical phase of drug development, the drug is studied in patients with the target disease to determine its efficacy: A. Phase 0 B. Phase 1 C. Phase 2 D. Phase 3 E. Phase 4
C
Phase 1 trial involves evaluation of doseresponse relationship and pharmacokinetics in normal volunteer patients with target disease. Phase 2 trial involves determination whether the agent has the desired efficacy at doses that are tolerated by sick pa
The most important pharmacologic action of digitalis in the treatment of heart failure is its ability to:
A. Increase heart rate
B. Reduce venous pressure
C. Reduce arterial pressure
D. Produce diuresis in edematous patients
E. Increase myocardia
E
The most important pharmacologic action of digitalis in the treatment of heart failure is its ability to increase myocardial contractile force by inhibiting Na/K ATPase and increaseing intracellular calcium.
Reserpine blocks this step of adrenergic transmission:
A. Synthesis of the neurotransmitter
B. Transport of neurotransmitter to vesicles
C. Release of the neurotransmitter
D. Reuptake into the presynaptic neuron
E. Diffusion in the synaptic cleft
B
Reserpine blocks vesicular transport in adrenergic transmission.
A 25 year-old farmer was brought to the emergency room after having allegedly drank a poison. PE revealed that he had constricted pupils, excessive salivation and sweating, wheezing and had several bouts of vomiting and diarrhea. He was given antidotes At
E
Pralidoxime is a cholinesterase regenerator, an antidote for organophosphate poisoning. Pralidoxime is an example of chemical antagonism. Chemical antagonism is when an antagonist directly interacts with the drug being antagonized to remove it or preve
It is the major second messenger of beta receptor activation that participates in signal transduction: A. Inositol triphosphate B. cAMP C. cGMP D. Calcium E. Adenylyl cyclase
B
cAMP is the major second messenger of beta receptor activation that participates in signal transduction.
A neonate was given IV antibiotics for 3 days. However, the baby developed hypothermia associated with diarrhea and grayish color of the skin. What is the mechanism of action of the drug that was given to the baby?
A. Inhibits transpeptidation in bacteri
C
Chloramphenicol is the drug that was given to neonate causing gray baby syndrome. It inhibits transpeptidation at 50s subunit and it is bacteriostatic. Penicillin inhibits transpeptidation in bacterial cell walls. Aminoglycoside inhibits protein synthe
It is a drug that is used almost solely as an alternative treatment for gonorrhea in patients whose gonococci are resistant to other drugs is: A. Docycycline B. Spectinomycin C. Ofloxacin D. Azithromycin E. Tetracycline
B
Spectinomycin is an aminoglycoside that inhibits protein synthesis by binding to 30s subunit. It is the drug of choice of drug-resistant gonorrhea and for gonorrhea in penicillin-allergic patients.
Drugs like quinidine, procainamide and disopyramide are very useful in treatment of: A. Congestive heart failure B. Hypertension C. Thyrotoxicosis D. Status asthmaticus E. Arrhythmia
E
Drugs like quinidine, procainamide and disopyramide are very useful in treatment of arrhythmia.
It is an anticonvulsant that is effective for neuropathic pain: A. Valproic acid B. Gabapentin C. Phenytoin D. Duloxetine E. Levetiracetam
B
Gabapentin is an anticonvulsant drug, a GABA derivative which blocks calcium channels, increases GABA release, very useful in neuropathic pain also in postherpetic neuralgia.
A 43 year-old male was diagnosed with Pulmonary Tuberculosis. He was given Anti-TB medications. However, he developed hyperuricemia. Which among these drugs inhibits the excretion of urate causing the above findings:
A. Ethionamide
B. Streptomycin
C
D
Pyrazinamide provoke avute gouty arthritis by inhibiting urate excretion.
A 28 year-old woman wanted to get pregnant. A substance that enhances probability of ovulation by blocking the inhibitory effect of estrogen and thus stimulating the release of gonadotrophin from the pituitary is:
A. Tamoxifen
B. Danazol
C. Clomi
C
Clomiphene citrate enhances probability of ovulation by blocking the inhibitory effect of estrogen and thus stimulating the release of gonadotrophin from the pituitary.
Upon taking Penicillin, a 20 year-old male suddenly experienced respiratory distress. A drug would be most helpful to treat the respiratory symptoms was given in this patient. In comparison to norepinephrine, epinephrine has more effects on:
A. alpha 1
D
Epinehrine is a sympathomimetic, nonselective and direct-acting. It is helpful in patients with anaphylactic shock. Respiratory distress is treated by Epinephrine’s action on beta 2 receptors resulting to bronchodilation.
Warfarin is prescribed to a 40 year-old male. The excessive anticoagulant effect results to bleeding in this patient can be reversed by:
A. Administration of vitamin K
B. Administration of fresh frozen plasma
C. Discontinuance of the drug
D. A
E
Bleeding with warfarin can be reversed by administration of Vitamin K, FFP and by discontinuance of the drug.
An anticancer agent that is prescribed for melanoma: A. Carmustine B. Cytarabine C. Vincristine D. Vinblastine E. Cisplatin
A
Carmustine is an alkylating agent, cell cycle non-specific that is given for melanoma.
An antihelminthic agent for strongyloidiasis: A. Nifurtimox B. Praziquantel C. Ivermectin D. Diethylcarbamazine E. Niclosamide
C
Ivermectin is the drug of choice for strongyloidiasis. It intensifies GABAmediated neurotransmission in nematodes and immobilizes parasites.
A 60 year-old female patient was diagnosed with breast cancer. She was given an alkylating agent, Cyclophosphamide. Later in the treatment, she developed hemorrhagic cystitis due to this toxic metabolite:
A. Amifostine
B. Acrolein
C. Mercaptopuri
B
Acrolein is the metabolite of Cyclophosphamide that causes hemorrhagic cystitis.
Chlorpromazine may be used not only in treating schzophrenia but is also effective in: A. Reducing nausea and vomiting B. Allergies C. Hypertension D. Treating bipolar disorders E. Sleep disorders
A
Chlorpromazine may be used not only in
treating schzophrenia but is also effective
in reducing nausea and vomiting.
The best treatment option for an obese patient with Type 2 Diabetes Mellitus is: A. Glibenclamide B. Metformin C. Repaglinide D. Acarbose E. Insulin
B
Metformin is a biguanide which is the first-line treatment for Type 2 DM, also a drug of choice for obese diabetics.
A 10 year-old child with asthma was prescribed with a drug which inhibits binding of leukotriene D4 to its receptor on target tissues. The drug prescribed is: A. Zileuton B. Ipratropium C. Montelukast D. Omalizumab E. Theophylline
C
Montelukast blocks leukotriene receptor for leukotrienes C4, D4, E4 preventing airway inflammation and bronchoconstriction in asthmatic patients.
The most dangerous hallucinogenic agent. A. LSD B. phencyclidine C. MDMA D. cocaine E. Marijuana
B
A 50 year old smoker, hypertensive patient complained of 2 month cough and dyspnea. He was on Carvedilol for his hypertension. What is the side effect of this drug that aggravates the condition.
A. bronchospasm
B. bronchoconstriction
C. tachycard
A
Mr. X was maintaining an unrecalled drug for the past few months. He is now complaining of visual changes or "yellow halo vision". What is the drug that is known to cause such effect? A. amiodarone B. ethambutol C. digoxin D. furosemide E.
C
A 45 year old male complained of chest pain upon exertion but relieved by rest. The doctor prescribed him a beta blocker. What is the effect of beta blocker? A. Increase oxygen supply B. Decrease oxygen demand C. Increase oxygen demand D. decr
B
drugs used in angina pectoris are the following: those that increase the oxygen supply are: nitrates and calcium blockers; those that decrease the oxygen demand are: beta blockers and still calcium blockers
Monday disease is caused by occupational exposure to: A. lead B. dust C. arsenic D. nitrates E. Gun powder
D
What is the predominant form of a weakly acidic drug with pKa of 5 at physiologic pH? A. Unprotonated charged B. Protonated charged C. Unprotonated uncharged D. Protonated uncharged E. None of the choices
A
The physiologic pH is at 7.35-7.45 which is above the pKa of this drug 5. At pH above pKa, weakly acidic drug is predominantly unprotonated charged, if it is below pKa, the predominant form is protonated uncharged.
It is the flow or transfer of a drug to the bloodstream. A. distribution B. bioequivalence C. absorption D. bioavailability E. Elimination
C
Absorption is the transfer of a drug to the bloodstream. Distribution is the entry of a drug to the target organ. Elimination is the termination of drug action. Bioavailability is the fraction of a drug that reaches the systemic circulation. Bioequival
What type of muscarinic receptors is used by the heart? A. M1 B. M2 C. M3 D. N1 E. N2
B
M1 - nerve endings, M2-heart, M3 - smooth muscle, glands, endothelium
Rivastigmine is used for: A. Motion sickness B. Myasthenia gravis C. Schizophrenia D. Parkinson's disease E. Alzheimer's disease
E
Rivastigmine is a cholinomimetic drug used for Alzheimer’s disease.
The drug that is used for cardiogenic shock as a last resort A. epinephrine B. dopamine C. dobutamine D. norepinephrine E. Vasopressin
D
A 58 year old male hypertensive was diagnosed with benign prostatic hyperplasia. What is the antihypertensive drug that is the most selective for prostatic smooth muscle? A. prazosin B. tamsulosin C. losartan D. metoprolol E. Terazosin
B
Alpha1 blockers are antihypertensive that is also used for BPH. Prazosin, tamsulosin, and terazosin are alpha1 blockers, but the most selective for prostatic smooth muscle is tamsulosin
A 75 year old male diabetic, hypertensive and a diagnosed case of CHF came in due to edema and dyspnea. If the patient had hypokalemia, a potassium sparing diuretic is indicated. This potassium sparing diuretic inhibits ENaC - epithelial sodium channel in
E
Spironolactone, triamterene, and amiloride are all potassium sparing diuretic. Triamterene and amiloride inhibit the ENaC of collecting duct, while spironolactone inhibits aldosterone receptor in collecting ducts.
A 100kg male patient had elevated LDL and VLDL. What vitamin is also used as antihyperlipidemic drug? A. Vitamin A B. pyridoxine C. niacin D. resin E. Cholestyramine
C
What is the drug of choice for paroxysmal supraventricular tachycardia? A. Esmolol B. adenosine C. verapamil D. Sotalol E. Any of the choices
B
Esmolol, sotalol, verapamil are all used for the treatment of supraventricular tachycardia. For paroxysmal supraventricular tachycardia, the drug of choice is adenosine.
A 10 year old child, known asthmatic had episodes of nocturnal asthma attacks approximately 2- 3x/week. In order to prevent subsequent attack, what drug is used for prophylaxis against nocturnal attack? A. Salbutamol + Ipratropium B. Salbutamol C.
E
Salbutamol is the druig of choice for acute asthma attack, while aminophylline is used for prophylaxis against nocturnal attacks.
A 4 year old child, febrile at 38deg. C was given Paracetamol at 15mkd. What is the mechanism of action of this drug?
A. COX-2 selective inhibitor
B. IL-1 and IL-6 inhibitors
C. COX-3 selective inhibitor
D. Irreversible COX-1 and COX-2 inhibi
C
Paracetamol or acetaminophen selectively inhibits COX-3. COX-2 selective inhibitors are coxib such as celecoxib. Irreversible COX-1 and 2 inhibitor is aspirin. TNF - ? inhibitors are infliximab, adalimumab and etanercept.
One of the choices does not belong to the third generation cephalosporins. A. cefotaxime B. ceftazidime C. ceftriaxone D. cefoxitin E. Ceftizoxime
D
All of the choices except cefoxitin are all third generation cephalosporin. Cefoxitin is a second generation.
A 32 year old G2P1 mother delivered a live term baby Boy with an upturned nose, mild midfacial hypoplasia, long upper lip, and lower distal digital hypoplasia. Upon review of maternal history, the mother was taking an anti-epileptic drug. The drug that is
A
The physical description of the neonate is consistent with fetal hydantoin syndrome which is the side effect of phenytoin
A 50 year old obese patient was diagnosed to have DM type 2. There were no other comorbidities. What hypoglycemic drug should you prescribed with this patient? A. Insulin B. Gliclazide C. Metformin D. Pioglitazone E. Sitagliptin
C
Metformin is the first line treatment for type 2 DM and is the drug of choice for obese patients. It is contraindicated in patients with renal disease,
Penicillin is the drug of choice for syphilis. It acts through: A. Inhibition of transpeptidase B. Inhibition of topoisomerase II C. Inhibition of glucan synthase D. Inhibition of D-alaD-ala terminus E. None of the choices
A
Penicillin inhibits transpeptidase enzyme needed for the bacterial cell wall synthesis. Vancomycin inhibits D-ala D ala synthase. Caspofungin inhibits glucan synthase. Flouroquinolone inhibits topoisomerase II and IV.
Marc, an asthmatic, is on theophylline. He has a number of other medical conditions. Which of the following medications may be safely administered with theophylline? A. Penicillin B. Erythromycin C. Phenytoin D. Rifampicin
A
Theophylline has a narrow therapeutic window and drug interactions can lead to severe morbidity. Erythromycin decreases the clearance of theophylline and increases its serum levels. Phenytoin and rifampicin have the oppositve effect. Advice: Memorize t
What is the maximum dose of Vincristine? A. 100 micrograms B. 200 micrograms C. 1 milligram D. 2 milligrams
D
SIMILAR TO PREVIOUS BOARD EXAM CONCEPT/PRINCIPLE
A pregnant patient complains of multiple external genital warts. Which of the following agents can be used in this patient? A. Podofilox solution B. Imiquimod cream C. Trichloroacetic acid D. Sinecatechins ointment
C
The most common treatments for genital warts in pregnancy are cryotherapy, laser removal, and trichloroacetic acid. The rest of the choices are under Pregnancy Category C.
The drug of choice for leptospirosis is: A. Doxycycline B. Penicillin C. Ceftriaxone D. Erythromycin
B
SIMILAR TO PREVIOUS BOARD EXAM CONCEPT/PRINCIPLE The rest of the choices are alternate drug choices for leptospirosis.
A 23-year-old presents with abdominal pain, tenesmus, and mucoid diarrhea with frank blood. Which is the best empiric treatment? A. Ciprofloxacin B. Metronidazole C. Amoxicillin D. Cotrimoxazole
A
Ciprofloxacin is the recommended empiric treatment for patients with acute dysenteriae. SIMILAR TO PREVIOUS BOARD EXAM CONCEPT/PRINCIPLE
The most powerful hallucinogen known to man is: A. LSD B. marijuana C. methamphetamine D. phencyclidine
A
It is the only licensed chemotherapy drug for advanced melanoma: A. adriamycin B. bleomycin C. cisplatin D. Dacarbazine
D
Plasma magnesium levels should be maintained at this therapeutic range to prevent eclamptic convulsions: A. 2-4 meq/L B. 4-7 meq/L C. 8-10 meq/L D. 10-12 meq/L
B
This is the only ligandgated serotonin receptor: A. 5HT1 B. 5HT2 C. 5HT3 D. 5HT4
C
This autonomic drug should be given with caution in patients with depressive disorders: A. guanethidine B. metyrosine C. vesamicol D. Reserpine
D
Reserpine which crosses the blood brain barrier is notorious for causing depression and increasing suicidal tendencies.
If a patient has COPD, which of the following beta-blockers would be more preferrable to use, theoretically? A. propranolol B. carvedilol C. labetalol D. Atenolol
D
Atenolol, metoprolol, esmolol, betaxolol, and acebutolol (A-BEAM) are more beta1-selective hence are advantageous in patients with comorbid pulmonary disease.
An 8-year-old being treated with a combination of chemotherapeutic agents had difficulty eating and drinking due to red, inflamed sores in her mouth and esophagus. Which of the following antineoplastic agents is the most likely etiology?
A. Methotrexat
A
Major toxicities of methotrexate include gastrointestinal mucositis, bone marrow suppression, skin erythema and hepatic dysfunction. SIMILAR TO PREVIOUS BOARD EXAM CONCEPT/PRINCIPLE
A young boy with G6PD deficiency would note tea-colored urine after the intake of which drug/s: A. primaquine B. cotrimoxazole C. nitrofurantoin D. All of the above
D
This drug activates peroxisome proliferator-activated receptors, a group of nuclear receptors, with greatest specificity to PPAR-? receptors: A. pioglitazone B. gemfibrozil C. sitagliptin D. Exenatide
A
Do not confuse with the mechanism of action of fibrates which is activation of the nuclear transcription factor PPAR-?.
Constipation is one of the major side effects of this drug: A. Magnesium hydroxide B. Aluminum hydroxide C. Omeprazole D. Colchicine
B
Aluminum hydroxide causes constipation (ALang tae). Magnesium hydroxide causes diarrhea (MaGtatae). Colchicine also causes diarrhea if taken in excess.
A patient presents with petit mal seizures. The drug of choice for this type of seizure is: A. phenytoin B. topiramate C. ethosuximide D. Lamotrigine
C
Petit mal seizures, also known as absence seizures, involves a brief, sudden lapse of consciousness. The DOC is ethosuximide.
A psychotic patient on haloperidol presents with rigidity, hyperpyrexia and autonomic instability. This condition is known as: A. Serotonin syndrome B. Neuroleptic malignant syndrome C. Tardive dyskinesia D. Malignant hyperthermia
B
Tardive dyskinesia is also one of the toxicities of antipsychotics aside from NMS. It is a condition where the patient presents with stereotypic oral-facial movements.
This diuretic can also be used in the treatment of glaucoma: A. acetazolamide B. hydrochlorothiazide C. mannitol D. Amiloride
A
Technically, mannitol can also be used but acetazolamide is a better answer. SIMILAR TO PREVIOUS BOARD EXAM CONCEPT/PRINCIPLE
It is a monoclonal antiIgE antibody used in the treatment of asthma resistant to inhaled steroids and long-acting B2-agonists: A. trastuzumab B. rituximab C. infliximab D. Omalizumab
D
Trastuzumab aka herceptin is a monoclonal antibody that interferes with the HER2/neu receptor, rituximab is against the protein CD20 on B cells, and infliximab is against TNF-alpha.
This drug inhibits platelet aggregation by irreversibly blocking ADP receptors: A. cilostazol B. tirofiban C. alteplase D. Ticagrelor
D
Cilostazol is a phosphodiesterase III inhibitor, tirofiban binds to GP IIb/IIIa receptor, and alteplase is a thrombolytic (not an anti-platelet) which converts plasminogen to plasmin.
These drugs act by preventing the binding of the agonist molecule to the receptor but do not activate generation of a signal: A. Pharmacologic antagonists B. Inverse agonists C. Competitive agonists D. Partial agonists E. Orphan drug
A
Katzung 10th ed, p. 11 - Pharmacologic anatgonists bind to the receptor preventing agonist binding thereby blocking the agonist’s biologic actions.
This route of drug administration is the most convenient, however bioavailability may be less than 100% because of incomplete absorption and firstpass elimination. A. Intramuscular B. Subcutaneous C. Oral D. Transdermal E. All of the above
C
Katzung 10th ed, p. 41
Loca is a 23 year old G4P4 (4004) who has been on oral contraceptives for 8 months now. What is the expected drug-drug interaction If she was to start on an antituberculosis drug that acts by inhibitting RNA synthesis and which imparts orange color to uri
E
Rifampin revs up the cytochrome P450 enzyme system thereby enhancing the metabolism and hence the elimination of the oral contraceptive the patient is taking resulting to its significantly lower serum level. Katzung 10th ed, p.774.
It is during this phase of drug development and testing that the effects of the drug as a function of dosage are established in a small number of healthy volunteers. A. Phase 1 B. Phase 2 C. Phase 3 D. Phase 4 E. Phase 5
A
Phase 1 trials determine the probable limits of the safe clinical dosage range in a small number of healthy volunteers. In Phase 2, the drug is studied in patients with the target disease to determine its efficacy. In phase 3, the drug is evaluated in
Which of the following drugs lower blood pressure by preventing normal physiologic release of norepinephrine from postganglionic sympathetic neurons? A. Metyrosine B. Cocaine C. Reserpine D. Botulinum toxin E. Guanethidine
E
Metyrosine inhibits tyrosine hydroxylase which is responsible for the conversion of Tyrosine to Dopa, the rate-limiting step in catecholamine synthesis. Cocaine blocks re-uptake of NE from the synaptic cleft thereby prolonging its effect. Reserpine blo
A tricyclic antidepresssant drug long used to reduce incontinence in institutionalized elderly patients and in children with bedwetting problems because of its strong anti-muscarinic actions: A. Ipratropium B. Imipramine C. Scopolamine D. Oxybutin
B
Katzung 115: Ipratropium-is an antimuscarinic drug used as an inhalational drug for asthma. Scopolamine- is an antimuscarinic drug used to remedy seasickness. Oxybutinin- is an antimuscarinic selective for M3 receptors used to relieve bladder spasm aft
Which of the following statements regarding diuretics is not true?
A. Diuretics lower blood pressure primarily by depleting body sodium stores.
B. The most common adverse effect of thiazide diuretics is potassium depletion.
C. The intercalated cells in
D
The collecting tubule and not the distal tubule is the final site NaCl reabsorption. It is responsible for tight regulation of body fluid volume and for determining the final sodium concentration of the urine. Katzung 10th ed., 239.
Which of the following drug acts by selectively inhibitting stimulation of B1 adrenoceptor and may be advantageous in treating hypertensive patients who also suffer from asthma, diabetes, or peripheral vascular disease?
A. Nadolol
B. Metoprolol
C. Pro
B
Katzung 10th ed., 169. Metoprolol, Esmolol, Atenolol, Acebutolol, Betaxolol, Bisoprolol are selective B1-blockers. Propranolol and Nadolol are nonselective B-blockers. Labetalol and Carvedilol have combined alpha and bblocking activity.
It is a very efficacious orally active arteriolar vasodilator that is also available in topical preparations used to stimulate hair growth for correction of baldness. A. Minoxidil B. Sodium Nitroprusside C. Hydralazine D. Diazoxide E. Fenol
A
Katzung 10th ed, 173.
A Class I-B antiarrhythmic drug which has a high degree of effectiveness in arrhythmias associated with acute myocardial infarction. A. Quinidine B. Flecainide C. Propranolol D. Lidocaine E. Amiodarone
D
Katzung 10th ed., 225 Quinidine- Class IA, associated with cinchonism; Flecainide- Class IC, very effective in suppressing premature vebtricular contractions; Propranolol-Class 2, Amiodarone-broad spectrum of actions
A potent antiandrogen that is usually coadministered with leuprolide that has been used in the treatment of prostatic carcinoma that frequently causes gynecomastia and occassionally mild reversible hepatic toxicity:
A. Goserelin
B. Spironolactone
C.
E
Katzung 10th ed., 679. this is SIMILAR TO PREVIOUS BOARD EXAM CONCEPT/PRINCIPLE
Disulfiram causes extreme discomfort in patients who drink alcoholic beverages by inhibitting which enzyme resulting to accumulation of acetaldehyde causing flushing, throbbing headache, nausea, vomiting, sweating, hypotension and confusion within few hou
B
Katzung 10th ed., 371. this was SIMILAR TO PREVIOUS BOARD EXAM CONCEPT/PRINCIPLE
The following helminths are matched with their respective drug of choice except:
A. Fasciola hepatica - Bithionol
B. Echinococcus granulosus - Albendazole
C. Stongyloides stercoralis - Thiabendazole
D. Schistosoma mansoni - Praziquantel
E. Dracunculu
C
The drug of choice in strongylodiasis and onchocerciasis that acts by intensifying GABA-mediated transmission of signals in peripheral nerves resulting to paralysis of the worms is Ivermectin. Thiabendazole is an alternative drug only. Katzung 10th ed.
What is the drug of choice for the eradication of dormant liver forms of Plasmodium vivax and Plasmodium ovale? A. Quinidine B. Primaquine C. Mefloqione D. Chloroquine E. Lumefantrine
B
Primaquine is the only available agent active against the dormant hypnozoite stages of p. vivax and p. ovale. (radical cure) Katzung 10th ed., 852
This halogen in a 1:20,000 solution is bactericidal in 1 minute and kills spores in 15 minutes. It is the most active antiseptic for intact skin: A. Phenol B. Hypochlorus acid C. Sodium hypochlorite D. Iodine E. Hexachlorophene
D
Katzung 10th ed., 822. Phenolic disinfectants are the oldest of the surgical antiseptics. They are used for hard surface decontamination in hospitals and labs. They are no longer used as a disinfectant because of its corrosive effect on tissues, its to
This antiviral agent against Influenza A acts by blocking the M2 proton ion channel of the virus particle and by inhibitting uncoating of the viral RNA within infected host cells, thus preventing its replication.
A. Amantadine
B. Ribavirin
C. Ose
A
katzung 10th ed., 815.
This drug is a derivative of rifamycin which is indicated in place of rifampin for treatment of tuberculosis in HIVinfected patients who are receiving concurrent protease inhibitors: A. Rifapentine B. Rifabutin C. Ritonavir D. Rifadin E. Ri
B
Katzung 10th ed., 777. Rifabutin is a less potent inducer of the cytochrome P450 enzyme (compared to Rifampin) resulting to slower elimination and longer halflife of protease inhibitors used in treating HIV patients is cases of HIV with concurrent tube
A 35 year old woman came to your clinic because of dysuria. She has been experiencing burning on urination with increased frequency and urgency to urinate for 5 days now. Urinalysis revealed WBC of 20-30/hpf, bacteria=moderate, nitrite=positive. You may p
D
Quinolones act by blocking bacterial DNA synthesis by inhibitting bacterial topoisomerase II and IV. Moxifloxacin is the only non-renally cleared fluoroqionolone and thus achieves low urinary level making it ineffective for cases of UTI. Katzung 10th e
The following are true of sulfonamides except:
A. Sulfonamides are structural analogs of paminobenzoic acid and act by inhibitting dihydropteroate synthase and folate production.
B. Sulfonamides are very effective against rickettsiae.
C. Combination of
B
It is interesting that rickettsiae are not inhibitted by sulfonamides but are actually stimulated in their growth. Katzung 10th ed., 763.
A 45 year old soldier has been maintaining on fluoxetine for his major depressive disorder. Which of the following drugs can precipitate a potentially fatal syndrome of hypertension, hyperreflexia, tremor, clonus, hyperhtermia, diarrhea, mydriasis and agi
E
This is a case of serotonin syndrome which is a condition precipitated when MAO inhibitors are given with serotonin agaonists, especially antidepressants of the SSRI class. Amytriptyline and Imipramine are TCAs. Fluoxetine, Sertraline and Citalopram ar