Drug elimination calculator

Table of contents

What is drug elimination half-life?

Drug elimination half-life is the time it takes for half of the drug to leave the blood. 

  • When we take medicine, our body breaks it down and removes it. The half-life is how long it takes for half of the medicine to be removed from our blood.


Drug half-life helps doctors know how much medicine to give, and what is a safe dose.

  • Different people need different amounts of medicine. By knowing the half-life, doctors can choose the right amount of medicine and when to give it to reduce harm from taking the medicine.

Why does drug half-life differ between people?

People have different bodies and health.

Some people have faster or slower body processes.

Age, weight, and gender can change drug half-life.

People have different bodies and health:

  • Some people are healthy, and some have health problems for example liver and kidney disease. This can change how fast their body processes drugs. 


Some people have faster or slower body processes:

  • Our bodies work at different speeds. This means some people's bodies will break down drugs faster or slower than others.


Age, weight, and gender can change drug half-life:

  • Older people, people who weigh more, and men or women can process drugs differently. This changes the drug half-life.


Some people take other medicines that can affect drug half-life:

  • If you take more than one medicine, they can interact. This can change how fast your body breaks down each drug.


People's genes can also make drug half-life different:

  • Genes are like instructions inside our bodies. They can tell our bodies to process drugs faster or slower. This makes drug half-life different in different people.

How to use drug elimination calculator

  1. Enter the date and time the drug was taken.
  2. Put in the amount of drug taken (in mg).
  3. Enter the half-life (time for drug to reduce by half).
  4. Click "Calculate."

This drug elimination calculator gives you an idea of how long it may take for a drug to leave the body.


The calculator is based on 'first order kinetics' which means it only works for drugs that leave the body at an even rate.


Keep in mind that the actual time can vary because it depends on many different things about the person and the drug.

Drug elimination calculator

Drug Elimination Half-Life Calculator
Enter the amount of drug taken in mg (e.g., 50)
Enter the half-life in hours (e.g., 12)
Date and Time (Hours) Drug Concentration (mg) Percentage of Starting Dose (%)

FAQs

Q1. What Is The Difference Between Elimination And Excretion?


  • Elimination refers to the removal of a drug from the body, which can happen through:
    • excretion (removal of drugs and their metabolites from the body) as well as
    • other processes such as metabolism (chemical changes in the body that transform drugs into different substances) and other bodily functions.


  • Excretion specifically refers to the removal of drugs or their by-products from the body through:
    • urine
    • faeces
    • sweat
    • breath

Q2. What Are The Main Ways Drugs Are Excreted From The Body?


  • Drugs are primarily excreted from the body through several main pathways:
    • urinary excretion via the kidneys
    • biliary excretion into the bile and then faeces
    • pulmonary excretion as a gas through the lungs
    • extra-renal excretion through sweat and saliva
  • Each of these processes contributes to the removal of drugs from the body.

Q3. What Are The Major Factors That Can Affect Drug Elimination?


  • Several major factors can affect drug elimination, including
    • kidney function (how well the kidneys work)
    • liver function (how well the liver works)
    • age of the person taking the drug
    • genetic (inherited) factors
    • interactions with other drugs or substances.
  • The body's ability to eliminate drugs can be influenced by these factors, which may affect how long a drug stays in the body and how it is processed.

Q4. What Is The Difference Between Metabolism And Excretion?


  • Metabolism is the process in which the body changes a drug into different substances (metabolites) through chemical reactions, mostly occurring in the liver.
    • These metabolites can be less active, more active, or equally as active as the original drug


  • Excretion, on the other hand, is the removal of drugs and their metabolites from the body, happening primarily through urine, faeces, sweat, or breath.

Q5. What Is Pharmacokinetics And Pharmacodynamics?


  • Pharmacokinetics is how our body processes medicine, whilst pharmacodynamics is how medicine affects our body.
  • To help remember what each means, try this:
    • Pharmaco-go-kinetics: How medication - moves - through the body
    • Pharmaco-do-dynamics: What medication - does - to the body.

Q6. What Are The 4 Steps of Pharmacokinetics?


  • The 4 Steps of Pharmacokinetics:
    • Absorption: Medications enter our bodyThis can happen by swallowing a pill, getting a shot, or breathing in a mist.
    • Distribution: Medications spread inside the bodyThe medicine travels through your body. It mixes with your blood and goes to different parts of your body.
    • Metabolism: Medications change form in our bodyYour body breaks down the medicine and changes it. This makes it easier for your body to use the medicine or to get rid of it.
    • Excretion: Medications leave our bodyAfter your body uses the medicine, it gets rid of what's left. This happens when you go to the bathroom or when you breathe out.

Q7. What Is An Example of Pharmacodynamics?


  • Here are 4 examples showing pharmacodynamics in action:
    • An antihistamine medicine helps reduce allergy symptoms like itching. The antihistamine blocks histamine, a chemical that causes allergies. This action helps stop itching.
    • A decongestant medicine helping clear a stuffy nose.The decongestant shrinks swollen nasal tissues. This allows air to flow and clears a stuffy nose.
    • Insulin helping our body use sugar. Insulin acts like a bridge helping sugar move from our blood to our cells for energy.
    • Loperamide an anti-diarrheal slows down the movement of food in your gut. It helps the body take more time to get water from food. This helps make stools less watery.

References

1. Anderson, Gail D. (2002). Children versus Adults: Pharmacokinetic and Adverse-Effect Differences. Epilepsia, 43, pp.53–59. doi:https://doi.org/10.1046/j.1528-1157.43.s.3.5.x. Link


2. Andrade, C. (2022). The Practical Importance of Half-Life in Psychopharmacology. The Journal of Clinical Psychiatry, [online] 83(4), p.41940. doi:https://doi.org/10.4088/JCP.22f14584. Link


3. Borowy, C.S. and Ashurst, J.V. (2019). Physiology, Zero and First Order Kinetics. [online] Nih.gov. Available at: https://www.ncbi.nlm.nih.gov/books/NBK499866/. Link  


4. Ernstmeyer, K. and Christman, E. (2023). Chapter 1 Pharmacokinetics & Pharmacodynamics. [online] National Library of Medicine. Available at: https://www.ncbi.nlm.nih.gov/books/NBK595006/. Link


5. Fernandez, E., Perez, R., Hernandez, A., Tejada, P., Arteta, M. and Ramos, J. (2011). Factors and Mechanisms for Pharmacokinetic Differences between Pediatric Population and Adults. Pharmaceutics, [online] 3(1), pp.53–72. doi:https://doi.org/10.3390/pharmaceutics3010053. Link


6. Heel, R.C., Brogden, R.N., Speight, T.M. and Avery, G.S. (1978). Loperamide. Drugs, 15(1), pp.33–52. doi:https://doi.org/10.2165/00003495-197815010-00003. Link


7. Home, P.D. (2012). The Pharmacokinetics and Pharmacodynamics of rapid-acting Insulin Analogues and Their Clinical Consequences. Diabetes, Obesity and Metabolism, 14(9), pp.780–788. doi:https://doi.org/10.1111/j.1463-1326.2012.01580.x. Link


8. Hoshitsuki, K., Fernandez, C.A. and Yang, J.J. (2021). Pharmacogenomics for Drug Dosing in Children: Current Use, Knowledge, and Gaps. The Journal of Clinical Pharmacology, 61(S1). doi:https://doi.org/10.1002/jcph.1891. Link


9. Mangoni, A.A. and Jackson, S.H.D. (2004). Age-related Changes in Pharmacokinetics and pharmacodynamics: Basic Principles and Practical Applications. British Journal of Clinical Pharmacology, [online] 57(1), pp.6–14. doi:https://doi.org/10.1046/j.1365-2125.2003.02007.x. Link


10. Naqvi, A. and Gerriets, V. (2020). Cetirizine. [online] PubMed. Available at: https://www.ncbi.nlm.nih.gov/books/NBK549776/. Link


11. Roth, R.P., Cantekin, E.I., Bluestone, C.D., Welch, R.M. and Cho, Y.W. (1977). Nasal Decongestant Activity of Pseudoephedrine. Annals of Otology, Rhinology & Laryngology, 86(2), pp.235–242. doi:https://doi.org/10.1177/000348947708600216. Link