Drug concentration | C = C0 e−kt | C = drug concentration at time t after C0 |
| | C0 = drug concentration at reference time |
| | k = elimination rate constant |
| | t = time between C and C0 |
Elimination rate constant | k = ln2/T0.5 | k = elimination rate constant |
| | ln2 = 0.693 |
| | T0.5 = half clearance time |
Volume of distribution | V = amount in body (μg)/actual C0 | V = volume of distribution |
| | Actual C0 = concentration at time of administration |
Area under curve | AUC0–∞ = FD/Vk | AUC0–∞ = area under curve (total drug dose) from time 0 to infinity |
| | F = fraction of drug absorbed |
| | D = dose |
| | V = volume of distribution |
| | k = elimination rate constant |
Clearance | CL = k × V | CL = clearance |
| | k = elimination rate constant |
| | V = volume of distribution |
Time to maximum concentration | Tmax = (1/[ka − k]) ln (ka/k) | Tmax = time to maximum concentration |
| | ka = absorption rate constant |
| | k = elimination rate constant |