Pharmacy Calculations: cram pack

Formula sheets, the key method steps for every topic and 6 practice problems, with full solutions at the back.

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1Formulas and methods

Pharmacy calculations

Percentage strength
% w/v = g per 100 mL
Amount in a solution
g = % × mL / 100
Ratio strength
1:X = 1 g in X mL; % = 100 / X
Reconstitution
final volume = diluent + powder volume
Concentration
mg/mL = drug in vial / final volume
Alligation
parts of H = T − L, parts of L = H − T
Water or base
0%

Dosage calculations

Dose from strength
volume = dose / strength
Weight-based dose
dose = mg/kg × body weight
Tablets
number = dose / tablet strength
Units
1 g = 1000 mg, 1 mg = 1000 mcg

Method

  1. Convert the ordered dose and the stock strength to the same unit.
  2. Use desired over have times quantity: (D/H) × Q.
  3. For weight-based doses, multiply by the weight in kg first, then divide the daily dose by the number of doses.
  4. Estimate first and check that the answer is reasonable.

Clinical pharmacokinetics

Rate constant and half-life
k = ln 2/t½ = 0.693/t½
First-order decay
C = C₀·e−kt = C₀·(1/2)t/t½
Two levels
k = ln(C₁/C₂)/Δt
Volume and clearance
Vd = dose/C₀, CL = k·Vd
Loading dose
LD = Vd·C/(S·F)
Maintenance rate
R = CL·Css/(S·F)
Average steady state
Css,avg = S·F·D/(CL·τ)
Steady state
1 − (1/2)ⁿ after n half-lives; ≈ 97% after 5
Infusion
C = (R/CL)(1 − e−kt)
Interval and dose from peak and trough
τ = ln(Cpeak/Ctrough)/k, D = Vd·(Cpeak − Ctrough)
Cockcroft–Gault
CrCl = (140 − age) × kg/(72 × SCr mg/dL), × 0.85 for women
Renal adjustment
dose × CrCl/normal; Dettli Q = 1 − fe·(1 − CrCl/normal)

Method

  1. Convert the half-life to a rate constant: k = 0.693/t½.
  2. Turn per-kg values into totals: Vd (L) = L/kg × weight, CL (L/h) = L/kg/h × weight.
  3. Pick the relation: C = C₀·e−kt, LD = Vd·C/(S·F), maintenance rate = CL·Css/(S·F), τ = ln(Cpeak/Ctrough)/k.
  4. For kidney function, estimate CrCl with Cockcroft–Gault first, then scale the dose or the interval.
  5. Check the result: levels fall by half every half-life, and steady state takes about five half-lives.

2Practice problems

1.Pharmacy calculationsMedium
ceftriaxone 2 gAdd 19.2 mL sterile water.Powder volume: 0.8 mL.? mg/mL

Practice exercise (made-up values, not clinical guidance). A vial contains ceftriaxone 2000 mg as a powder. The practice label says to add 19.2 mL of sterile water; the powder adds 0.8 mL to the volume. What is the concentration C in mg/mL after reconstitution?

2000 mg19.2 mL+0.8 mL
C = mg/mL
2.Pharmacy calculationsHard
70%dextrose? mL+10%dextrose25%100 mL

Practice exercise (made-up values, not clinical guidance). You must prepare 100 mL of 25% dextrose by mixing 70% and 10% dextrose. How many mL V of the 70% solution do you need? Round to the nearest whole mL.

70%10%25%100 mL
V = mL
3.Dosage calculationsMedium
500 mg+ 4.6 mLV = ? mL

A vial contains 500 mg of powder. The label says: add 4.6 mL of water for injection to give a total volume of 5 mL. The prescription is 80 mg. What volume V of the reconstituted solution do you give?

500 mg+ 4.6 mL → 5 mL80 mg
V = mL
4.Dosage calculationsHard
41 kg125 cmBSA = √(h·w/3600)25 mg/m²D = ? mg

A patient is 125 cm tall and weighs 41 kg. The prescription is 25 mg/m². Using the Mosteller formula BSA = √(height (cm) × weight (kg)/3600), find the dose D in mg.

125 cm41 kg25 mg/m²
D = mg
5.Clinical pharmacokineticsMedium
110100t (h)C (mg/L)C₀ = 12 mg/Lt½ = 2 hC₀/2

Practice exercise (made-up values, not clinical guidance). A patient receives an IV bolus of 330 mg of gentamicin. The level back-extrapolated to time zero is 12 mg/L and the half-life is 2 h. Find the volume of distribution Vd.

D = 330 mgC₀ = 12 mg/Lt½ = 2 h
Vd = L
6.Clinical pharmacokineticsHard
t (h)C (mg/L)Css​6 hC = ?

Practice exercise (made-up values, not clinical guidance). A vancomycin infusion runs at 80 mg/h with no loading dose. The patient's clearance is 4 L/h and the half-life is 8 h. What is the level C after 6 h?

R = 80 mg/hCL = 4 L/ht½ = 8 ht = 6 h
C = mg/L

3Solutions

1.Pharmacy calculations

Answer: C = 100 mg/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

19.2 + 0.8 = 20 mL

Concentration

C = 2000/20 = 100 mg/mL

Answer

C = 100 mg/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

70%: 25 − 10 = 15 parts
10%: 70 − 25 = 45 parts
total: 60 parts

Share the volume

V = 100·15/60 = 25 mL

Answer

V = 25 mL

Check: 25 mL of 70% + 75 mL of 10% = 100 mL.

3.Dosage calculations

Answer: V = 0.8 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.

Concentration after mixing

500 mg/5 mL = 100 mg/mL

Volume

V = 80/100 = 0.8 mL

Answer

V = 0.8 mL
4.Dosage calculations

Answer: D = 29.83 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 = √(125·41/3600) = √1.424 = 1.193 m²

Dose

D = 25·1.193 = 29.83 mg

Answer

D = 29.83 mg
5.Clinical pharmacokinetics

Answer: Vd = 27.5 L

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.

Volume of distribution

Vd = 330/12 = 27.5 L

Answer

Vd = 27.5 L
6.Clinical pharmacokinetics

Answer: C = 8.108 mg/L

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.

Steady-state level

Css = 80/4 = 20 mg/L

Rate constant

k = 0.693/8 = 0.08664 h⁻¹

Level after the given time

C = 20·(1 − e−0.08664·6) = 8.108 mg/L

Answer

C = 8.108 mg/L

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