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
penicillin G 5 000 000 unitsdiluent addedconcentration18.2 mL250 000 units/mL8.2 mL500 000 units/mL3.2 mL1 000 000 units/mL400 000 units → ? mL

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 400 000 units. What volume V do you draw up? Round to one decimal place.

8.2 mL → 500 000 units/mL400 000 units
V = mL
2.Pharmacy calculationsHard
70%dextrose+10%dextrose? mL25%1000 mL

Practice exercise (made-up values, not clinical guidance). You must prepare 1000 mL of 25% dextrose by mixing 70% and 10% dextrose. How many mL V of the 10% solution do you need? Round to the nearest whole mL.

70%10%25%1000 mL
V = mL
3.Dosage calculationsMedium
0.5%w/vV = ? mL

A dose of 20 mg is needed from a 0.5% (w/v) solution. What volume V contains this dose?

20 mg0.5% w/v
V = mL
4.Dosage calculationsHard
125 mg/5 mLV = ? mL

A child weighing 28 kg is prescribed 15 mg/kg per dose of an oral suspension that contains 125 mg in 5 mL. What volume V do you give?

28 kg15 mg/kg125 mg/5 mL
V = mL
5.Clinical pharmacokineticsMedium
110t (h)C (mg/L)C₀ = 7 mg/Lt½ = 3 hC₀/2

Practice exercise (made-up values, not clinical guidance). A patient receives an IV bolus of 200 mg of tobramycin. The level back-extrapolated to time zero is 7 mg/L and the half-life is 3 h. Find the clearance CL in L/h.

D = 200 mgC₀ = 7 mg/Lt½ = 3 h
CL = L/h
6.Clinical pharmacokineticsHard
Vd = 7 L/kg0.5 → 1 mcg/LLD = ? mcg67 kg · S = 1 · F = 0.7

Practice exercise (made-up values, not clinical guidance). A 67 kg patient has a digoxin level of 0.5 mcg/L; the target is 1 mcg/L. The volume of distribution is 7 L/kg and the tablets have F = 0.7. What extra loading dose LD raises the level to the target?

67 kgVd = 7 L/kgC = 0.5 → 1 mcg/LF = 0.7
LD = mcg

3Solutions

1.Pharmacy calculations

Answer: V = 0.8 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.

Concentration from the label

8.2 mL → 500 000 units/mL

Volume to give

V = 400 000/500 000 = 0.8 mL

Answer

V = 0.8 mL
2.Pharmacy calculations

Answer: V = 750 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 = 1000·45/60 = 750 mL

Answer

V = 750 mL

Check: 250 mL of 70% + 750 mL of 10% = 1000 mL.

3.Dosage calculations

Answer: V = 4 mL

Solution strengths: a percentage strength is grams per 100 mL, so 1% = 1 g/100 mL = 10 mg/mL. A ratio strength 1:1000 means 1 g in 1000 mL = 1 mg/mL; 1:10 000 is 0.1 mg/mL. For a dilution the amount of drug stays the same: C₁·V₁ = C₂·V₂.

Concentration

0.5% = 5 mg/mL

Volume

V = 20/5 = 4 mL

Answer

V = 4 mL
4.Dosage calculations

Answer: V = 16.8 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.

Dose from weight

15·28 = 420 mg

Volume

V = (420/125)·5 = 16.8 mL

Answer

V = 16.8 mL
5.Clinical pharmacokinetics

Answer: CL = 6.601 L/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.

Volume of distribution

Vd = 200/7 = 28.57 L

Rate constant

k = 0.693/3 = 0.231 h⁻¹

Clearance

CL = 0.231·28.57 = 6.601 L/h

Answer

CL = 6.601 L/h
6.Clinical pharmacokinetics

Answer: LD = 335 mcg

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 = 7·67 = 469 L

Rise needed

1 − 0.5 = 0.5 mcg/L

Loading dose

LD = 469·0.5/(1·0.7) = 335 mcg

Answer

LD = 335 mcg

In practice the dose is rounded to a convenient amount.

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