front 1 A pharmacy student is completing a drug interaction screening for a
patient with a new prescription for paroxetine, a known CYP enzyme
inhibitor. The pharmacy student notes the effect of taking paroxetine
with each of the following medications: | back 1 Tamoxifen is a prodrug, carvedilol is an active substrate, tramadol is a prodrug |
front 2 Drug A is an active substrate of enzyme X. Drug B is an inhibitor of enzyme X. A patient has been using Drug A with good results. The patient has now started therapy with Drug B. The concentration of Drug A will: | back 2 Increase (Drug A is an active substrate of enzyme X. An inhibitor of this enzyme will be added. Inhibitors knock out the ability of the enzyme to metabolize the drug, by various mechanisms such as changing the shape of the enzyme via binding or depletion of a co-factor required for metabolism. Without enough enzyme present, the concentration of substrates will increase as the liver breaks down less.) |
front 3 Which of the following are CYP3A4 inhibitors? | back 3 Ritonavir, diflucan, grapefruit |
front 4 A patient has an estimated creatinine clearance of 25 mL/min. Her potassium level is 4.8 mEq/L. Which of the following drugs will increase her risk of hyperkalemia and should be used with caution? | back 4 Enalapril |
front 5 A patient who is a CYP450 2D6 rapid metabolizer is using codeine for pain. What effect will the 2D6 polymorphism have on the concentration of morphine? | back 5 The morphine concentration will increase (The conversion of codeine to morphine is increased in rapid metabolizers of 2D6. Codeine should be avoided in women who are breastfeeding because often, the 2D6 variant is unknown. Morphine crosses readily into breast milk, and the infant could suffer fatal respiratory depression. Codeine is contraindicated in children under 12 years of age, and in children under 18 years of age after tonsillectomy and adenoidectomy.) |
front 6 Which cytochrome P450 enzyme is not inducible? | back 6 2D6 |
front 7 Which drug/s can increase the QT interval? (Select ALL that apply.) | back 7 Quinolones, methadone and amitriptyline |
front 8 Drug A is a substrate of CYP2C9 and a potent 3A4 inhibitor. Drug B is a substrate of 2D6 and 1A2 as well as a potent inhibitor of 2C19. Drug C is a substrate of 3A4 and a potent inhibitor of 2D6. If all three drugs were given together, what would the levels of each drug be expected to do? | back 8 Drug A levels would stay the same, Drug B levels would increase and Drug C levels would increase (Drug C inhibits CYP2D6 and increases levels of Drug B (substrate of 2D6). Drug A inhibits 3A4 and increases levels of Drug C (substrate of 3A4). Neither Drug B nor Drug C inhibits or induces 2C9 and therefore, levels of Drug A remain the same.) |
front 9 A patient with asthma, COPD and seizures has been using theophylline and valproate for many years. The patient has been under a lot of stress lately and has started smoking again. She smokes about 15-20 cigarettes daily. Which of the following statements is correct about smoking? | back 9 Smoking will decrease the theophylline level. |
front 10 VN uses Imitrex for migraines 2-4 times each month. Recently she began to use Sarafem 10 mg daily for premenstrual dysphoric disorder. In addition, she uses Ultram once or twice daily for headache relief. She is at risk for the following symptoms: (Select ALL that apply.) | back 10 Agitation, rigidity |
front 11 Which of the following drugs can cause hearing loss? (Select ALL that apply.) | back 11 Vancomycin, gentamicin, ethacrynic acid and salicylates can cause hearing loss, tinnitus or vertigo. |
front 12 A patient is using digoxin. If he is prescribed the following drug, the digoxin serum concentration will increase: | back 12 Verapamil (Verapamil is a P-gp inhibitor, and digoxin is a P-gp substrate. ) |
front 13 A patient with atrial fibrillation has been using warfarin for nine months, and his INR is stable around 2.3. The patient has been diagnosed with depression and asked for a prescription that will not interact with his other medications. Which of the following drugs will not increase the bleeding risk in this patient? | back 13 Wellbutrin |
front 14 Clopidogrel is a prodrug metabolized by CYP2C19. What effect will a CYP2C19 inhibitor have? | back 14 Decreased antiplatelet effect immediately |
front 15 Chief Complaint: shortness of breath History of Present Illness: SZ is a 77-year-old female admitted to the hospital on April 7th for worsening shortness of breath that she describes as much worse than her "typical heart failure episodes." In addition, SZ states that she has been experiencing episodes of nausea and blurry or double vision over the past couple of weeks. Allergies: penicillin (rash and lip swelling) Past Medical History: COPD, heart failure (last EF 30%), alcoholism Home Medications: Altace 10 mg daily, Lasix 40 mg BID, Coreg CR 40 mg daily, Digox 0.25 mg daily, Combivent Respimat 1 inhalation QID, Procardia XL 60 mg daily, Aldactone 25 mg daily SZ should be counseled to avoid drinking grapefruit juice to prevent increased levels of which medication? | back 15 Procardia XL |
front 16 ( same case as above) During her hospital stay, SZ develops atrial fibrillation. What adjustment should be made to her home medications if amiodarone is added to her regimen? | back 16 Decrease digoxin to 0.125 mg daily |
front 17 A patient is at risk for atrial fibrillation; she has had atrial fibrillation in the past. The medical team has asked the pharmacist to check for drugs on her profile that can increase her risk of arrhythmia. The pharmacist should include which of the following medications? | back 17 Ziprasidone |
front 18 Which of the following are inhibitors of CYP450 3A4? | back 18 Voriconazole (Vfend), clarithromycin ( Biaxin), diltiazem ( Cardizem) and grapefruit (juice and fruit) are all CYP3A4 inhibitors. |
front 19
Chief Complaint: "I'm here for my flu vaccine
but my stomach hurts" | back 19 CNS depression |
front 20 Which of the following are P-gp substrates? | back 20 Important P-gp substrates include the calcineurin inhibitors tacrolimus and cyclosporine, colchicine, and the anticoagulants dabigatran, apixaban and rivaroxaban. |
front 21 BH takes an estrogen and progestin combination oral contraceptive (COC). She recently received a prescription for phenytoin. Which of the following best describes the interaction between these medications? | back 21 Phenytoin is a potent inducer. Inducers result in higher levels of CYP enzymes, which decrease levels of substrate drugs (e.g., estrogen). |
front 22 Drug metabolism occurs most often through which CYP450 enzyme? | back 22 3A4 |
front 23 Theophylline is a substrate of CYP1A2. A patient on long-term theophylline, who has been well-controlled with infrequent use of her rescue inhaler, has developed a UTI that is difficult to treat. The physician prescribed a 7-day course of ciprofloxacin. Which of the following is most likely to occur? | back 23 Possible theophylline toxicity |
front 24 A 74-year-old woman had been taking metoprolol succinate 100 mg daily, warfarin 4 mg daily and amitriptyline 50 mg QHS for several years. Shortly after the death of her spouse, she experienced some depression and was prescribed citalopram 40 mg daily. The patient is most at risk for: | back 24 Torsade de Pointes |
front 25 Drug A is an active drug substrate of enzyme X. Drug B is an inducer of enzyme X. A patient has been using Drug A with good results. The patient has now started therapy with Drug B. The concentration of Drug A will: | back 25 Decrease (Drug A is a substrate of enzyme X, which is being induced by another drug. That means the other drug (Drug B) is causing more enzyme X to be produced. More of the enzyme will result in more metabolism of Drug A, and the concentration will decrease.) |
front 26 Phosphodiesterase inhibitors (e.g., tadalafil) cannot be used safely with nitrates. What is most likely to happen if a pharmacist misses this interaction? | back 26 Acute drop in blood pressure |
front 27 GV has been using a monoamine oxidase inhibitor to help control her depression for many years. She is careful to check that other drugs and foods do not interact with her medicine. Which of the following drugs should be avoided with GV's antidepressant? (Select ALL that apply.) | back 27 Methylphenidate and claritin-D |
front 28 Select the correct statements concerning the drug interaction between valproic acid and lamotrigine. (Select ALL that apply.) | back 28
|
front 29 Cyclosporine is an inhibitor of the P-glycoprotein (P-gp) efflux transporter. If a drug is a substrate of P-gp, what will happen to the drug concentration if it is given to a patient receiving cyclosporine? | back 29 The concentration of the substrate will increase |
front 30 A 65-year-old woman brings a new prescription for a monoamine oxidase inhibitor to the pharmacy. Which of the following foods should she be counseled to avoid? | back 30 Sauerkraut |
front 31 A patient with atrial fibrillation has been using warfarin for four months, and his INR is stable around 2.3. Select the interaction that can occur with the addition of these other medications: | back 31 If naproxen is added, the INR may or may not increase and the bleeding risk will be elevated |
front 32 Which of the following is an inducer of CYP450 3A4? | back 32 Phenobarbital, pacerone |
front 33
History of Present Illness: BG is a 71-year-old male
who presents to the hospital with a 6-day history of non-bloody
diarrhea that he believes may be a side effect of donepezil. He has
had no sick contacts or changes to his usual diet. He denies fever,
sweating, chills, chest pain, shortness of breath, nausea or vomiting. | back 33 The effects of warfarin will increase |
front 34 (same case from above) While verifying medication orders, the pharmacist receives an alert about a medication that is a CYP1A2 inhibitor. Which medication, from home or newly ordered on admission, meets this criteria? | back 34 Cipro |
front 35 Which of the following drugs interacts with grapefruit? | back 35 Tacrolimus |
front 36 Which of the following statements best describes warfarin metabolism? | back 36 Warfarin is racemic; the S-isomer is more potent and is primarily a substrate of CYP2C9 |
front 37 TW has been taking phenelzine (Nardil) for many years to treat depression. Which drug will interact with TW's antidepressant? | back 37 Tramadol |
front 38 Drug A is a substrate of enzyme X. Drug A is also an inducer of enzyme Y. Drug B is a substrate of enzyme Y. Drug B is also an inhibitor of enzyme X. When these drugs are both administered, what will happen to the concentrations of Drug A and Drug B? | back 38 Levels of drug A will increase and levels of drug B will decrease (Drug A is a substrate of an enzyme that is being inhibited and Drug B is a substrate of an enzyme that is being induced.) |
front 39 CL is being placed on the waiting list for a kidney transplant. She has a creatinine clearance of 22 mL/min and experiences frequent bouts of hyperkalemia. Which medications elevate potassium and would put her at risk for arrhythmia? (Select ALL that apply.) | back 39 Eplerenone, yasmin, aldactone |
front 40 A patient with a deep vein thrombosis has been using warfarin for four months, and his INR is stable around 2.5. Which of the following interactions is correct? | back 40 If rifampin is added, the INR will decrease (CYP2C9 inducers (which decrease the INR) include phenobarbital, phenytoin, primidone, rifampin (large decrease in INR) and St. John's wort.) |
front 41 Which of the following are CYP450 enzyme inducers? (Select ALL that apply.) | back 41 Phenytoin, oxcarbazepine, carbamazepine and St. John's wort are CYP450 enzyme inducers. Neoral is cyclosporine, which is a CYP450 enzyme inhibitor. |
front 42 Which of the following drugs increase the risk of a patient having a fall that could result in injury? (Select ALL that apply.) | back 42 Muscle relaxants, mirtazapine and benzodiazepines are central nervous system (CNS) depressants. CNS side effects are caused by drugs that enter the CNS (lipophilic) and result in sedation (somnolence), dizziness, confusion (decreased cognitive function) and altered consciousness. |
front 43 Which medication must have the dose reduced by 30-50% if amiodarone is added to the same patient profile? | back 43 Warfarin (The dose of warfarin should be decreased by 30-50% when beginning amiodarone.) |
front 44 LD is a 74-year-old African American female who is being admitted to
a nursing home. Her family can no longer care for her at home due to
increasing episodes of urinary incontinence. The nursing home admitting orders for LD include Ultram 50 mg PO Q4H as needed for pain. The pharmacist verifying the order receives a drug interaction alert warning of an increased risk of: | back 44 Serotonin syndrome |
front 45 A major drug interaction can occur with the use of grapefruit juice and which of the following medications? | back 45 Lovastatin and nifedipine |
front 46 What can occur if a CYP450 3A4 inhibitor is given to a patient on oxycodone? (Select ALL that apply.) | back 46 Respiratory depression and sedation |
front 47 MT is taking Aggrenox, torsemide, Crestor, Toprol XL, Lotensin, Cardizem, Klor-Con, Nitrostat PRN, fish oil and DHEA. Based on his medication list, MT is most at risk for: | back 47 Bradycardia |
front 48 A patient with atrial fibrillation has been using warfarin for nine months, and his INR is stable between 2.3-2.7. What is most likely to occur if he starts taking ginkgo biloba? | back 48 The INR will stay at about the same and the bleeding risk will increase |
front 49 Which of the following statins has the lowest risk of drug interactions? | back 49 Pravastatin (Atorvastatin, lovastatin, simvastatin and fluvastatin are all metabolized by CYP450 enzymes. When taken with an inhibitor, the risk of myopathy is increased. In severe cases, rhabdomyolysis can occur, which may lead to acute renal failure. To avoid this interaction, recommend a statin not metabolized by CYP450 enzymes (e.g., pravastatin, rosuvastatin).) |
front 50 Which of the following drugs can cause hearing loss? (Select ALL that apply.) | back 50 Loop diuretics, vancomycin, aminoglycosides, cisplatin and salicylates are drugs that can cause ototoxicity. |