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NAPLEX

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Question
Answer
Medications that interact with warfarin   "ACADEMIC FACS" Amiodarone Ciprofloxacin/levofloxacin Aspirin Dicloxacillin Erythromycin (Macrolides) Metronidazole (Azoles) Indomethacin Clofibrates Fibrates Allopurinol CYP 2C9 Inducers/inhibitors Statins  
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Amiodarone- drug interactions   -Digoxin -Warfain =decrease dose of digoxin or warfarin by 30-50% when starting amiodarone  
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Digoxin- drug interactions   -increase in levels: likely due to decreased renal function -toxicity more likely if potassium low -P-gp substrate, narrow therapeutic range -caution with drugs that lower INR: beta blockers, non-dhp CCBs, amiodarone, dexmedetonidine (Precidex), clonidine, opioids  
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Grapefruit juice- interactions   inhibits CYP3A4 -simvastatin -lovastatin -nifedepine -tacrolimus  
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Lamotrigine and Valproate- drug interaction   severe rash  
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MAOIS, Opioids- interactions   -avoid with serotonergic drugs- serotonin syndrome -parkinson's drugs -washout period for MAOIs: 14 days -tyramine metabolism decreased with MAOIs: selegiline, rasagiline -Serotonergic drugs: ephedrine, lithium, meperidine, levodopa, Dextromethorphan, cyclobenzaprine, triptans etc.  
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Tramadol- drug interactions   -2D6 metabolized to active form -diministed effect on 2D6 inhibitors (fluoxetine, paroxetine, or poor metabolizers of 2D6)  
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Codeine- drug interactions   partial prodrug metabolized by 2D6 -ultrametabolizers, extensive metabolizers- OD risk -2D6 inhibitors, poor metabolizers = diminished effect  
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CYP450 enzyme inhibitors "BIGFACES.COM"   "BIGFACES.COM" Bupropion Itraconazole/ketoconazole/fluoxetine Gemfibrozil Fluoxetine/fluvoxamine Amiodarone Ciprofloxacin Erythromycin/Clarithromycin Sulfamethoxazole-trimethoprim Clopidogrel Omeprazole/Esomeprazole Metronidazole  
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CYP450 enzyme inducers   "PS PORCS" Phenytoin Smoking Phenobarbitol Oxcarbazepine Rifampin Carbamazepine St. John's Work  
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CYP450 enzyme inhibitors "G PACMAN"   "G PACMAN" Grapefruit Protease Inhibitors (ritonavir) Azole antifungals Cyclosporine, Cimetedine, Cobicistat Macrolides (except azithromycin) Amiodarone Non-DHP CCBs  
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Calcineurin Inhibiots- drug interactions   CYP substrates: Systemic azoles macrolides rifampin -nephrotoxic- avoid with aminoglycosides  
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Fentanyl, Hydrocodone, Oxycodone, Methadone- drug interactions   CYP3A4 inhibitors = fatal respiratory depression  
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PDE-5 Inhibitors- drug interactions   C/I with nitrates = severe hypotension -decrease doses of alpha blockers with PDE5 inhibitors -caution with CYP3A4 inhbitors- PDE5 inhibitors are substrates  
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Quinolones, tetracyclines- drug interactions   Chelation risk, seperate from vitamins, electrolytes  
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Statins- drug interactions   increased levels = increased muscle toxicity -most are CYP3A4 metabolites: atorvastatin, simvastatin, lovastatin  
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1 gallon   4 quarts 3840 mL (approx) 3785 mL (exact)  
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1 fluid oz   30 mL (approx) 29.57 mL (exact)  
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1 quart   2 pints 960 mL (approx) 946 mL (exact)  
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1 pint   16 oz 480 mL (approx) 473 mL (exact)  
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1 cup   8 oz 240 mL (approx) 236.56 mL (exact)  
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Use IBW for these drugs   -aminophylline -theophylline -acyclovir  
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Use AdjBw (if obese) for these drugs   aminoglycosides  
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Use TBW (if obese) for these drugs   -LMWHs -UFH -Vancomycin  
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When calculating CrCl- which body weight to use?   Underweight: TBW Normal: IBW Overweight/obese: AdjBW  
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Calcium+ Phosphate total should not exceed   45 MEQ/L (precipitates)  
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Hazard Ratio   Hazard rate in treatment group/ hazard rate in control group  
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Sensitivity   1- type II error(false negative)  
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Specificity   1- type I error (false positive)  
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Relative risk reduction   1- RR or (%risk in control- % risk in treatment)/ % risk in control  
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Odds ratio   (disease present, exposed to treatment)(disease absent, unexposed to treatment)/ (disease absent, exposed to treatment)(disease present, unexposed to treatment)  
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Number needed to treat   1/(risk in control-risk in treatment group) or 1/ARR  
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absolute risk reduction   %risk in control - % risk in treatment group  
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Risk   # of subjects with unfavorable events in arm/ total # of subjects in arm  
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Risk ratio   risk in treatment group/ risk in control group  
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Anion gap   Na- Cl- HCO3  
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Calcium conversions   Carbonate: 40% elemental calcium Citrate: 21% elemental calcium  
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% ionization of weak base   100/1 + 10^(pH-pKa)  
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% ionization of a weak acid   100/1 + 10^(pKa-pH)  
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ANC   WBC X (%segs + %bands/100)  
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Corrected calcium   Calcium reported (serum) + [(4-albumin)(0.8)]  
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Vd Equation   amount of drug in body/ concentration of drug in plasma  
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Cl Renal equals   Cl GFR + Cl secretion- Cl reabsorption  
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Cl renal > Cl GFR   filtration + net secretion  
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Cl GFR > Cl Renal   filtration + net reabsoprtion  
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Cl renal = Cl GFR   filtration only  
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Loading dose equation   desired concentration x Vd/F  
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Ke equation   Cl/Vd  
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Peak serum concentration equation   LD/Vd  
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Clearance equation (extravascular)   absolute bioavailability x dose/ AUC  
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steady state concentration equation   DR/Cl  
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half-life equation   0.693/Ke  
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Clearance equation (IV)   dose/AUC  
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clearance equation   rate of elimination/ concentration  
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acute bioavailability equation   100 X [(AUC extravascular)/(AUC intravascular)]x{(dose IV)/(dose extravascular)]  
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Codeine- pharmacogenomics   consider testing CYP450 2D6 -ultrametablizers = toxicity risk  
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Clopidogrel- pharmacogenomics   consider testing CYP2C19 genotype -*1 allelle = fully functional *2 and *3 = loss of function of alleles  
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Trastuzumab- pharmacogenomics   HER2 protein overexpression- required for use  
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Carbamazepine- pharmacogenomics   HLA-*1502 -test in Asian populations- increased risk of serious skin reactions  
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Abacavir- pharmacogenomics   HLA-B*571 -if positive, increased risk of hypersensitivity  
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Allopurinol- pharmacogenomics   consider testing HLA-B*5801 if positive, do not use- increased risk of SJS  
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Phenytoin- pharmacogenomics   consider testing HLA-B*1502 in all Asain populations-incrased risk of SJS and TEN  
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Azathioprine- pharmacogenomics   TPMT- low/absent activity = increased risk of myelosuppression  
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Capecitabine- pharmacogenomics   consider testing DPD deficiency- increased toxicity risk  
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Cetuximab- pharmacogenomics   KRAS- if positive, drug will not work  
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Warfarin- pharmacogenomics   Consider testing CYP450 2C9*2/*3 -VKORC1 = increased bleed risk  
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Thyroid function tests needed for these drugs   levothyroxine, armour thyroid, amiodarone, lithium, statins  
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Drugs that cause severe skin reactions   allopurinol, lamotrigine, penicillins, phenytoin, piroxicam, sulfamethoxazole  
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drugs that cause photosensitivity   carbamazepine, diruetics, methotrexate, retinoids, quinolones, st. john's wort, sulfa abx, tacrolimus, tetracyclines, voriconazole  
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drugs that cause TTP   clopidogrel, ticlopidine  
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avoid these drugs with peanut and soy allergies   progesterone (peanut), Clevidipine, propofol (Soy and eggs)  
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hyperkalemia risk with these drugs   -aldosterone blockers- avoid NSAIDS -ACEIs, ARBS, aliskerin, amiloride, triamterene, calcinuerin inhibitors, bactrim, cangliflozin, pentamadine  
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ototoxicity risk with these drugs   salicylates, vancomycin, aminoglycosides, cisplatin, loop diuretics  
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avoid these with drugs that have increased bleed risk   NSAIDs, SSRIs/SNRIs, ginko biloba, garlic, ginger, glucosamine, ginseng  
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