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 cefazolin 1000 mg as a powder. The practice label says to add 4.5 mL of sterile water; the powder adds 0.5 mL to the volume. The prescribed dose is 250 mg. What volume V do you draw up? Round to one decimal place.
1000 mg4.5 mL+0.5 mL250 mg
V = mL
2.Pharmacy calculationsHard
Practice exercise (made-up values, not clinical guidance). You must prepare 600 mL of 4% chlorhexidine from a 20% stock and purified water. How many mL V of water do you need? Round to the nearest whole mL.
20%0%4%600 mL
V = mL
3.Dosage calculationsMedium
A patient weighs 90 kg. The prescribed dose is 20 mg/kg per day, given in 2 equal doses. How many milligrams D are given per dose?
90 kg20 mg/kg/day2× per day
D = mg
4.Dosage calculationsHard
A patient is 134 cm tall and weighs 40 kg. The prescription is 75 mg/m². Using the Mosteller formula BSA = √(height (cm) × weight (kg)/3600), find the dose D in mg.
134 cm40 kg75 mg/m²
D = mg
5.Clinical pharmacokineticsMedium
Practice exercise (made-up values, not clinical guidance). After an IV dose of tobramycin, the level is 6 mg/L at 1 h and 1.5 mg/L at 7 h. Assume first-order elimination. Find the half-life t½.
C1 = 6 mg/L (1 h)C2 = 1.5 mg/L (7 h)
t½ = h
6.Clinical pharmacokineticsHard
Practice exercise (made-up values, not clinical guidance). A theophylline infusion is started without a loading dose. The half-life in this patient is 9 h. How long t does it take to reach 90% of the steady-state level?
t½ = 9 h90% Css
t = h
3Solutions
1.Pharmacy calculations
Answer: V = 1.3 mL
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
4.5 + 0.5 = 5 mL
Concentration
1000/5 = 200 mg/mL
Volume to give
V = 250/200 = 1.25 ≈ 1.3 mL
Answer
V = 1.3 mL
2.Pharmacy calculations
Answer: V = 480 mL
Alligation: to mix a higher strength H and a lower strength L into a target strength T, take (T − L) parts of H and (H − T) parts of L. The parts are crossed: each stock gets the distance from the target to the other stock. Water or a plain base counts as 0%. The numbers are for practice only; at the bedside always follow local protocols and have high-risk doses double-checked.
Alligation parts
20%: 4 − 0 = 4 parts
0%: 20 − 4 = 16 parts
total: 20 parts
Water
V = 600·16/20 = 480 mL
Answer
V = 480 mL
Check: 120 mL of 20% contains 24 g of drug, which is 4% of 600 mL.
3.Dosage calculations
Answer: D = 900 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
20·90 = 1800 mg
Per dose
D = 1800/2 = 900 mg
Answer
D = 900 mg
4.Dosage calculations
Answer: D = 91.52 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 = √(134·40/3600) = √1.489 = 1.22 m²
Dose
D = 75·1.22 = 91.52 mg
Answer
D = 91.52 mg
5.Clinical pharmacokinetics
Answer: t½ = 3 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.
Elimination rate constant
k = ln(6/1.5)/6 = 1.386/6 = 0.231 h⁻¹
Half-life
t½ = 0.693/0.231 = 3 h
Answer
t½ = 3 h
6.Clinical pharmacokinetics
Answer: t = 29.9 h
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.