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
ampicillin 500 mgAdd 1.8 mL sterile water.Powder volume: 0.2 mL.250 mg → ? mL

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. The prescribed dose is 250 mg. What volume V do you draw up? Round to one decimal place.

500 mg1.8 mL+0.2 mL250 mg
V = mL
2.Pharmacy calculationsHard
23%sodium chloride+3%sodium chloride? mL13%300 mL

Practice exercise (made-up values, not clinical guidance). You must prepare 300 mL of 13% sodium chloride by mixing 23% and 3% sodium chloride. How many mL V of the 3% solution do you need? Round to the nearest whole mL.

23%3%13%300 mL
V = mL
3.Dosage calculationsMedium
500 mg+ 9.6 mLV = ? mL

A vial contains 500 mg of powder. The label says: add 9.6 mL of water for injection to give a total volume of 10 mL. The prescription is 20 mg. What volume V of the reconstituted solution do you give?

500 mg+ 9.6 mL → 10 mL20 mg
V = mL
4.Dosage calculationsHard
83 kg168 cmBSA = √(h·w/3600)50 mg/m²D = ? mg

A patient is 168 cm tall and weighs 83 kg. The prescription is 50 mg/m². Using the Mosteller formula BSA = √(height (cm) × weight (kg)/3600), find the dose D in mg.

168 cm83 kg50 mg/m²
D = mg
5.Clinical pharmacokineticsMedium
10100t (h)C (mg/L)1 h30 mg/L11 h15 mg/L

Practice exercise (made-up values, not clinical guidance). After an IV dose of vancomycin, the level is 30 mg/L at 1 h and 15 mg/L at 11 h. Assume first-order elimination. Find the half-life t½.

C1 = 30 mg/L (1 h)C2 = 15 mg/L (11 h)
t½ = h
6.Clinical pharmacokineticsHard
t (h)C (mg/L)Css​11 hC = ?

Practice exercise (made-up values, not clinical guidance). A theophylline infusion runs at 20 mg/h with no loading dose. The patient's clearance is 2 L/h and the half-life is 9 h. What is the level C after 11 h?

R = 20 mg/hCL = 2 L/ht½ = 9 ht = 11 h
C = mg/L

3Solutions

1.Pharmacy calculations

Answer: V = 1 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

1.8 + 0.2 = 2 mL

Concentration

500/2 = 250 mg/mL

Volume to give

V = 250/250 = 1 mL

Answer

V = 1 mL
2.Pharmacy calculations

Answer: V = 150 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

23%: 13 − 3 = 10 parts
3%: 23 − 13 = 10 parts
total: 20 parts

Share the volume

V = 300·10/20 = 150 mL

Answer

V = 150 mL

Check: 150 mL of 23% + 150 mL of 3% = 300 mL.

3.Dosage calculations

Answer: V = 0.4 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/10 mL = 50 mg/mL

Volume

V = 20/50 = 0.4 mL

Answer

V = 0.4 mL
4.Dosage calculations

Answer: D = 98.4 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 = √(168·83/3600) = √3.873 = 1.968 m²

Dose

D = 50·1.968 = 98.4 mg

Answer

D = 98.4 mg
5.Clinical pharmacokinetics

Answer: t½ = 10 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(30/15)/10 = 0.6931/10 = 0.06931 h⁻¹

Half-life

t½ = 0.693/0.06931 = 10 h

Answer

t½ = 10 h
6.Clinical pharmacokinetics

Answer: C = 5.714 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 = 20/2 = 10 mg/L

Rate constant

k = 0.693/9 = 0.07702 h⁻¹

Level after the given time

C = 10·(1 − e−0.07702·11) = 5.714 mg/L

Answer

C = 5.714 mg/L

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