Pick the relation: C = C₀·e−kt, LD = Vd·C/(S·F), maintenance rate = CL·Css/(S·F), τ = ln(Cpeak/Ctrough)/k.
For kidney function, estimate CrCl with Cockcroft–Gault first, then scale the dose or the interval.
Check the result: levels fall by half every half-life, and steady state takes about five half-lives.
2Practice problems
1.Pharmacy calculationsMedium
Practice exercise (made-up values, not clinical guidance). A vial contains ampicillin 500 mg as a powder. The practice label says to add 1.8 mL of sterile water; the powder adds 0.2 mL to the volume. What is the concentration C in mg/mL after reconstitution?
500 mg1.8 mL+0.2 mL
C = mg/mL
2.Pharmacy calculationsHard
A vial holds 500 mg of powder. You add 3.6 mL of diluent, and the powder adds 0.4 mL of volume. The prescription is 425 mg. Draw up the dose: what volume V do you give?
500 mg3.6 mL + 0.4 mL425 mg
V = mL
3.Dosage calculationsMedium
A patient weighs 70 kg. The prescribed dose is 30 mg/kg per day, given in 4 equal doses. How many milligrams D are given per dose?
70 kg30 mg/kg/day4× per day
D = mg
4.Dosage calculationsHard
A patient is 138 cm tall and weighs 48 kg. The prescription is 60 mg/m². Using the Mosteller formula BSA = √(height (cm) × weight (kg)/3600), find the dose D in mg.
138 cm48 kg60 mg/m²
D = mg
5.Clinical pharmacokineticsMedium
Practice exercise (made-up values, not clinical guidance). Vancomycin is given as a continuous infusion to a patient whose vancomycin clearance is 60 mL/min. What infusion rate R in mg/h gives a steady-state level of 20 mg/L?
CL = 60 mL/minCss = 20 mg/L
R = mg/h
6.Clinical pharmacokineticsHard
Practice exercise (made-up values, not clinical guidance). An 80-year-old woman weighs 73 kg and has a serum creatinine of 1.3 mg/dL (115 µmol/L). Estimate the creatinine clearance with Cockcroft–Gault: CrCl (mL/min) = (140 − age) × weight (kg)/(72 × SCr in mg/dL), × 0.85 for women. The usual atenolol dose is 100 mg for a creatinine clearance of 100 mL/min, and a fraction fe = 0.9 of the drug is excreted unchanged by the kidneys. Using the Dettli dose fraction Q = 1 − fe·(1 − CrCl/normal CrCl), find the adjusted dose D. Round to the nearest whole number.
Reconstitution: the powder takes up space, so the final volume is the diluent plus the powder volume. Concentration = drug in the vial/final volume, and the volume to give = dose/concentration. On a multi-strength label, use the concentration that belongs to the amount of diluent you actually added. The numbers are for practice only; at the bedside always follow local protocols and have high-risk doses double-checked.
Final volume
1.8 + 0.2 = 2 mL
Concentration
C = 500/2 = 250 mg/mL
Answer
C = 250 mg/mL
2.Pharmacy calculations
Answer: V = 3.4 mL
Strength to volume: turn the strength into mg per mL first. A w/v percentage is grams per 100 mL, so x% = 10x mg/mL. A ratio strength 1:n is 1 g in n mL. After reconstitution the concentration is the powder's dose over the final volume (diluent + powder volume). Then volume = dose/concentration.
Final volume and concentration
3.6 + 0.4 = 4 mL
C = 500/4 = 125 mg/mL
Volume
V = 425/125 = 3.4 mL
Answer
V = 3.4 mL
3.Dosage calculations
Answer: D = 525 mg
Dose calculation: the amount to give equals what is prescribed divided by what you have, times the quantity it comes in: amount = (desired dose/stock strength) × stock volume. Always keep the units the same (convert g to mg, mg to mcg first) and check that the answer is sensible.
Total per day
30·70 = 2100 mg
Per dose
D = 2100/4 = 525 mg
Answer
D = 525 mg
4.Dosage calculations
Answer: D = 81.39 mg
Body-surface-area dosing: many cytotoxic and some paediatric doses are prescribed per square metre of body surface area: dose (mg) = dose per m² × BSA (m²). The Mosteller formula estimates BSA = √(height (cm) × weight (kg)/3600).
Body surface area
BSA = √(138·48/3600) = √1.84 = 1.356 m²
Dose
D = 60·1.356 = 81.39 mg
Answer
D = 81.39 mg
5.Clinical pharmacokinetics
Answer: R = 72 mg/h
Clearance and volume: at steady state the dosing rate equals the elimination rate, so the maintenance rate = CL × Css. A loading dose is LD = Vd × C/(S × F), with S the salt factor (fraction of active drug in the salt) and F the bioavailability (1 for IV). From two levels, k = ln(C₁/C₂)/Δt; for an IV bolus Vd = dose/C₀ and CL = k × Vd. The numbers are for practice only; at the bedside always follow local protocols and have high-risk doses double-checked.
Clearance in L/h
60·60/1000 = 3.6 L/h
Infusion rate
R = 3.6·20 = 72 mg/h
Answer
R = 72 mg/h
6.Clinical pharmacokinetics
Answer: D = 46 mg
Designing a regimen: with rapid IV doses the level falls from peak to trough during the interval, so τ = ln(Cpeak/Ctrough)/k and the dose that restores the peak is Vd × (Cpeak − Ctrough). The average steady-state level is Css,avg = S·F·dose/(CL·τ). An infusion rises as C = (R/CL)(1 − e−kt). For a drug cleared by the kidneys, the dose is scaled with the creatinine clearance. The numbers are for practice only; at the bedside always follow local protocols and have high-risk doses double-checked.
Creatinine clearance (Cockcroft–Gault)
CrCl = (140 − 80)·73/(72·1.3)·0.85 = 39.78 mL/min
Dose fraction (Dettli)
Q = 1 − 0.9·(1 − 39.78/100) = 0.458
Adjusted dose
D = 0.458·100 = 45.8 ≈ 46 mg
Answer
D = 46 mg
In practice the dose is rounded to a convenient amount and checked against the product information.