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 of penicillin G contains 5 000 000 units. Its practice label gives three strengths (see the table). You add 8.2 mL of diluent. The prescribed dose is 750 000 units. What volume V do you draw up? Round to one decimal place.
8.2 mL → 500 000 units/mL750 000 units
V = mL
2.Pharmacy calculationsHard
Practice exercise (made-up values, not clinical guidance). You must prepare 100 mL of 20% dextrose by mixing 50% and 10% dextrose. How many mL V of the 50% solution do you need? Round to the nearest whole mL.
50%10%20%100 mL
V = mL
3.Dosage calculationsMedium
A child weighing 6 kg is prescribed 10 mg/kg of a drug. The stock solution contains 10 mg/mL. Draw up the dose: what volume V do you give?
6 kg10 mg/kg10 mg/mL
V = mL
4.Dosage calculationsHard
A child weighing 8 kg is prescribed 5 mg/kg per dose of an oral suspension that contains 120 mg in 5 mL. What volume V do you give? Round to one decimal place.
8 kg5 mg/kg120 mg/5 mL
V = mL
5.Clinical pharmacokineticsMedium
Practice exercise (made-up values, not clinical guidance). After an IV dose of tobramycin, the level is 6 mg/L at 2 h and 1.5 mg/L at 8 h. Assume first-order elimination. Find the half-life t½.
C1 = 6 mg/L (2 h)C2 = 1.5 mg/L (8 h)
t½ = h
6.Clinical pharmacokineticsHard
Practice exercise (made-up values, not clinical guidance). A 67 kg patient takes oral theophylline (F = 1) every 12 h. The clearance is 0.035 L/kg/h. What dose D in mg gives an average steady-state level of 10 mg/L?
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.
Concentration from the label
8.2 mL → 500 000 units/mL
Volume to give
V = 750 000/500 000 = 1.5 mL
Answer
V = 1.5 mL
2.Pharmacy calculations
Answer: V = 25 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
50%: 20 − 10 = 10 parts
10%: 50 − 20 = 30 parts
total: 40 parts
Share the volume
V = 100·10/40 = 25 mL
Answer
V = 25 mL
Check: 25 mL of 50% + 75 mL of 10% = 100 mL.
3.Dosage calculations
Answer: V = 6 mL
Drawing up a dose: volume = (prescribed dose/stock strength) × stock volume. Convert to the same units first, then check that the volume fits the syringe and lands on one of its graduations.
Dose from body weight
D = 10·6 = 60 mg
Volume
V = 60/10 = 6 mL
On the syringe
On this 10 mL syringe every small line is 0.2 mL.
Answer
V = 6 mL
4.Dosage calculations
Answer: V = 1.7 mL
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.
Dose from weight
5·8 = 40 mg
Volume
V = (40/120)·5 = 1.667 ≈ 1.7 mL
Answer
V = 1.7 mL
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: D = 281.4 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.
Clearance
CL = 0.035·67 = 2.345 L/h
Dose
D = Css,avg·CL·τ/(S·F) = 10·2.345·12/(1·1) = 281.4 mg