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Pharmacokinetics - equations and therapeutic ranges mostly

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Question
Answer
goal range for flucytosine   50-100 mcg/ml  
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goal range for digoxin   0.8-2.0 mcg/L [typically 1.2 is the upper limit]  
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goal range for valproic acid   50-100 mg/L  
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Formula for loading dose   [Peak] * Vd / bioavailability  
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formula for the elimination rate constant or slope   [ln (y1)- ln (y2)] / x1-x2  
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formula for volume of distribution   dose/change in concentration = bioavailability * dose / peak conc (bolus) = rate of infusion / k* Css  
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formula for peak concentration   peak conc = concentration / e^kt t=time from peak for concentration.  
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formula for bioavailability   F= [DOSEiv * AUCpo] / [DOSEpo * AUCiv]  
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relationship between the elimination constant k, VD and clearance   Cl=k*VD  
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formula for half life   t1/2=0.693/k  
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in what way do isozymes affect fluconazole   at doses above 400 mg/day you get 3A4 inhibition but lower doses only have 2C9  
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Cockcroft -Gault formula for CrCl   CrCl=[(140-age)*TBW]/Scr*72 Women get 80% of total AdjBW if BMI >25 actualBW if BMI <18.5 all others use IBW  
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formula for IBW   men=50+2.3 for each inch over 5 ft women 45.5 +2.3 for each inch over 5 ft  
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what population is the schwartz eqn designed for   peds  
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what GFR equations work for pts with renal dysfunction   MDRD and CKDepi. MDRD is limited to pts with CrCl < 60 only.  
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drugs that compete with creatinine for secretion in pts resulting in false elevations in Creatinine clearance   trimethoprim, cimetidine, fibric acid derivatives OTHER than gemfibrozil, dronedarone  
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what does the hill eqn measure   relationship btn drug response and concentration  
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hysteresis   conc late after dose has diff effect than early with same conc  
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causes of counterclockwise hysteresis loop   delayed equilibrium between plasma and site of action, active metabolite, sensitization, Ex: digoxin  
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causes of clockwise hysteresis loop   tolerance, formation of inhibitory metabolite, faster equilibrium between arterial blood supply and site of action than venous and site of action. Ex: cocaine and pseudoephedrine  
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goal ranges, free and total for phenytoin   free=1-2 total=10-20  
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calculation for phenytoin adjustment in changing albumin   Cp=[Cp' / (0.9*Alb/4.4)]+1  
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calculation for phenytoin adjustment in CKD AND changing albumin   Cp=Cp' / [(0.48*0.9*Alb/4.4)+1]  
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calculation for phenytoin adjustment in CKD   Cp=Cp'/0.5  
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what is the effect on digoxin in pts with renal insufficiency   Vd decreases. need to decrease BOTH loading dose and maintenance dose. typically loading doses ok to keep same but not in this case due to lower VD for digoxin.  
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therapeutic range for aminoglycosides   peak 4-10, trough <2 amikacin 20-30 trough amikacin <10  
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phenobarbital therapeutic range   15-40 mg/L  
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therapeutic range for lithium   0.3-1.3 mmol/L  
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therapeutic range for carbamazepine   4-12 mg/L  
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therapeutic range for cyclosporine   100-250 mcg/L  
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theophylline therapeutic range   10-20 mg/L  
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concentration or time dependent killing for aminoglycosides   concentration  
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concentration or time dependent killing for vancomycin   time dependent though some concentration dependence as well  
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