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Pharmacy Calculations Cheat Sheet
Pharmacy Calculations Cheat Sheet
tsp (t) 5 ml between two strengths (pg 103 in RxPrep) Males = 50 kg + (2.3 kg)(# inches over 5 ft)
tbsp (T) 15 ml - Set up X method Females = 45.5 kg + (2.3 kg)(# inches over 5 ft)
1 fl oz 30 ml 29.57 ml (actual) - Subtract along the ‘X’ lines to obtain the
1 cup 8 oz 240 ml 236.58 ml number of parts on the right Adjusted Body Weight (AdjBW)
(actual) - Add the number of parts on the right to find AdjBW = IBW + 0.4(TBW – IBW)
1 pint 16 oz 480 ml 473 ml (actual) the total number of parts
1 quart 2 pints 960 ml 946 ml (actual) - Divide the total weight by number of parts to Cockcroft-Gault Equation
1 gallon 4 quarts 3840 3785 ml (actual) obtain weight per part CrCl (ml/min) = (140 – age)(Wt in kg) x
ml Not reliable in: (72)(SCr)
1 liter 1000 ml Osmolarity - very young children x 0.85 if female
Osmolarity = Wt (g/L) x # particles x 1,000 - ESRD patients
(mOsm/L) MW (g/mole) - rapidly fluctuating/unstable renal function
Common Solid Weight Conversions
1 kg 2.2 lbs
Compound # dissociation Calculating CrCl Dosing
1 oz 28.4 g ABW < IBW ABW < IBW
particles Under-
1 lb 454 g weight à use ABW à use ABW
Dextrose 1
1 grain (gr) 65 mg 64.8 mg (actual) Normal ABW > IBW & BMI <25 If < 120% of IBW
Mannitol 1
weight à use IBW à
KCl 2 use ABW– most drugs insulin
Common Distance Conversions
NaCl 2 use IBW– amino, theo, acyclovir,
1 inch 2.54 cm levothyroxine, IVIG
Na acetate (NaC2H3O2) 2
1 meter 100 cm Over- BMI ³ 25 If ³ 120% of IBW
Ca Chloride (CaCl2) 3 à use AdjBW à
weight insulin
Na citrate (Na3C6H5O7) 4 use ABW– LMWH, UFH, vanco
Order of Operations: use AdjBW– AGs
Brackets à Parentheses à Exponents à use IBW– amino, theo, acyclovir,
Isotonicity (pg. 107)
Multiplication/Division à Addition/Subtraction levothyroxine, IVIG
Osmolarity in context of body fluids
Expressed as NaCl equivalent or “E value”
Percentage Strength *notice grams* Calculating CrCl SMX:TMP 1:5
TDD by 1 unit of rapid-acting insulin CL = Rate of Elimination x= (x mg)/(x hours) total # of subjects in group
Concentration x mg/L
Rule of 450 (Regular): Relative Risk or Risk Ratio (RR) = AS LIKELY
450 = grams of carbohydrate covered CL = F x Dose CL = ke x Vd RR = Risk in treatment group x
TDD by 1 unit of regular insulin AUC Risk in control group
Correction Factor (add to usual dose!) Zero Order and First Order PK Relative Risk Reduction (RRR) = LESS LIKELY
1,800 Rule (Rapid-Acting): 1st order elimination = LINEAR kinetics = RRR = (% risk control group – % risk treatment group) x
1,800 = correction factor for 1 unit constant % of drug is removed per unit of time % risk control group
TDD of rapid-acting insulin RRR = 1 – RR(must use decimal)
1,500 Rule (Regular): Zero order elimination = NON-linear kinetics =
1,500 = correction factor for 1 unit constant amount of drug (mg) is removed per Absolute Risk Reduction (ARR)
TDD of regular insulin unit of time – non-linear ARR = (% risk in control group) – (% risk treatment group)
Correction Dose Most drugs follow 1st order (linear) kinetics Number Needed To Treat or Harm (NNT, NNH)
Correction dose = (BG now) – (target BG) - At steady state, doubling the dose will NNT or NNH = 1 x
correction factor ~double the serum concentration ARR* expressed as decimal
NNT – round up
Room Temperature Stability of Insulin and Michaelis-Menten Kinetics NNH – round down
Injectable Diabetes Medications Non-linear, saturable, or mixed order kinetics
Vials that are not 28 days - PHT initially follows first-order elimination Odds Ratio (OR)
Humulin vials (R, N, 70/30) 31 days - Once enzymes are saturated, PHT follows OR = AD x= (012 1)342561,
(012 1)342561,
012 45$&4'1)∗(94 1)342561, 94 45$&4'1)
94 45$&4'1)∗(94 1)342561, 012 45$&4'1)
Humulin U-500 vials 40 days zero order elimination BC
Novolin vials 42 days - Double the dose may more than double the
Levemir vial 42 days serum concentration Hazard Ratio (HR)
- The rate of metabolism approaches zero HR = Hazard rate in the treatment group x
Pens that are not 28 days
order at higher concentrations Hazard rate in the control group
Humalog Mix pen 10 days
- Increase in dose leads to a disproportionate
Humulin Mix pen 10 days Sensitivity
increase in drug concentration at steady state
Humulin N pen 14 days Sensitivity = A x 100 = TrueP x 100
- Ex: phenytoin, theophylline, voriconazole
Novolog Mix pen 14 days A+C TrueP + FalseN
Toujeo pen 42 days Elimination Rate Constant
Levemir pen 42 days Specificity
ke = CL xx ke = 0.693 x Specificity = B x 100 = TrueN x 100
Tresiba pen 56 days Vd t½
Others B+D TrueN + FalseP
Afrezza – opened strips 3 days Half-Life and Steady State Test HAVE No
Afrezza – unopened 10 days t½ = 0.693 x Result condition condition
Trulicity, Adlyxin 14 days ke Have outcome Do not have
outcome
Xultophy (degludec + liraglutide) 21 days
Positive A B
Bydureon, Soliqua (glargine + lixisenatide) 28 days Steady state: where rate of drug intake equals (yes- (TP) (FP)
Byetta, Victoza, Symlin 30 days rate of drug elimination exposure)
Negative C D
Ozempic 56 days (no-exposure) (FN) (TN)
~5 half-lives to reach steady state
Total A+C B+D
U-200:
- Humalog KwikPen (& U-100) ~5 half-lives are required to eliminated >95% of “It makes SENSe to be positive”
- Tresiba FlexTouch (& U-100) the drug
U-300: Sensitivity = true positive … disease present
- Toujeo Solostar/Max Solostar snOUT- sensitive test when negative rules OUT the disease
Loading Dose (LD)
U-500: LD = Desired concentration x Vd x Specificity = true negative … disease not present
- Humulin R (& U-100) F spIN- specific test when positive rules IN the disease
target levels are provided on naplex. maybe just know the target vs. indication for digoxin & vancomycin.
also maybe know whether which level you’re measuring (peak or trough) for the ones indicated