About Drug Half-Life and Elimination Kinetics
A drug's elimination half-life (t½) is the time required for the amount of drug in the body, or its concentration in the blood plasma, to drop by half. Most drugs are cleared by first-order kinetics, meaning the body eliminates a constant fraction of the remaining drug per unit time rather than a constant amount — so the half-life itself stays the same no matter how much drug is present. This calculator applies the standard first-order decay equation, C(t) = C0 × (1/2)(t / t½), to show how much of an initial dose or concentration remains after a chosen elapsed time, along with the elimination rate constant and the time until the drug is considered clinically cleared.
How the calculation works
Enter the initial dose or concentration (C0), the drug's published elimination half-life, and the time elapsed since the dose. The calculator first derives the elimination rate constant k = ln(2) / t½ (≈ 0.693 / t½), which is the fraction eliminated per hour. It then computes the remaining amount using the equivalent exponential form C(t) = C0 × e(-k × t), converts that to a percentage of the starting dose, and reports how many hours it would take to reach roughly 5 half-lives — the point at which about 96.9% of the drug has been eliminated and it is generally treated as cleared for practical purposes.
Why half-life matters
- Dosing intervals: drugs with a short half-life (a few hours) typically need more frequent dosing to keep levels in a therapeutic range; drugs with a long half-life (a day or more) may be dosed once daily.
- Time to steady state: with repeated dosing at a fixed interval, blood levels rise toward a plateau and reach roughly 90-97% of steady state after about 4-5 half-lives.
- Washout period: before starting a new medication that interacts with the current one, clinicians often wait about 5 half-lives of the first drug so it is substantially cleared.
- Individual variation: published half-life values come from population averages; a person's actual elimination rate can differ based on age, kidney and liver function, genetics, other medications, and hydration status.
Important limitations
This tool performs a simplified one-compartment, first-order elimination calculation. Many drugs follow more complex multi-compartment or non-linear (zero-order, saturable) kinetics, especially at high doses, and absorption or distribution phases are not modeled here. This calculator is for general education about pharmacokinetic concepts only — it does not calculate or recommend an actual dose, dosing schedule, or treatment decision. Always refer to the specific drug's prescribing information and consult a pharmacist or physician before making any medication decision.