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. What is the concentration C in mg/mL after reconstitution?
1000 mg4.5 mL+0.5 mL
C = mg/mL
2.Pharmacy calculationsHard
A vial holds 500 mg of powder. You add 3.2 mL of diluent, and the powder adds 0.8 mL of volume. The prescription is 262.5 mg. Draw up the dose: what volume V do you give?
500 mg3.2 mL + 0.8 mL262.5 mg
V = mL
3.Dosage calculationsMedium
A patient weighs 70 kg. The prescribed dose is 7.5 mg/kg per day, given in 2 equal doses. How many milligrams D are given per dose?
70 kg7.5 mg/kg/day2× per day
D = mg
4.Dosage calculationsHard
A patient weighs 52.8 lb. The prescription is 10 mg/kg as a single dose, and the stock contains 200 mg in 5 mL. Using 1 kg = 2.2 lb, what volume V do you give?
52.8 lb10 mg/kg200 mg/5 mL1 kg = 2.2 lb
V = mL
5.Clinical pharmacokineticsMedium
Practice exercise (made-up values, not clinical guidance). After an IV dose of tobramycin, the level is 8 mg/L at 1 h and 2.5 mg/L at 6 h. Assume first-order elimination. Find the half-life t½.
C1 = 8 mg/L (1 h)C2 = 2.5 mg/L (6 h)
t½ = h
6.Clinical pharmacokineticsHard
Practice exercise (made-up values, not clinical guidance). A 100 kg patient on regular gentamicin doses is at steady state. The target is a peak of 8 mg/L and a trough of 0.5 mg/L, and the volume of distribution is 0.3 L/kg. Assuming rapid IV doses, what dose D raises the level from the trough to the peak?
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
C = 1000/5 = 200 mg/mL
Answer
C = 200 mg/mL
2.Pharmacy calculations
Answer: V = 2.1 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
3.2 + 0.8 = 4 mL
C = 500/4 = 125 mg/mL
Volume
V = 262.5/125 = 2.1 mL
Answer
V = 2.1 mL
3.Dosage calculations
Answer: D = 262.5 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
7.5·70 = 525 mg
Per dose
D = 525/2 = 262.5 mg
Answer
D = 262.5 mg
4.Dosage calculations
Answer: V = 6 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.
Weight in kg
52.8/2.2 = 24 kg
Dose
10·24 = 240 mg
Volume
V = (240/200)·5 = 6 mL
Answer
V = 6 mL
5.Clinical pharmacokinetics
Answer: t½ = 2.98 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(8/2.5)/5 = 1.163/5 = 0.2326 h⁻¹
Half-life
t½ = 0.693/0.2326 = 2.98 h
Answer
t½ = 2.98 h
6.Clinical pharmacokinetics
Answer: D = 225 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.
Volume of distribution
Vd = 0.3·100 = 30 L
Dose
D = 30·(8 − 0.5) = 225 mg
Answer
D = 225 mg
In practice the dose is rounded to a convenient amount.