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Digoxin

Drug Monitoring

Dig levelLanoxin level

Review status

Currently under review

Pending specialist review and validation.

What it shows

Digoxin is a heart medicine used to help control certain irregular heart rhythms and to ease symptoms in some people with heart failure. This blood test measures how much digoxin is in your bloodstream, showing how your body is absorbing and clearing the drug at the time of sampling.

Levels vary with dose timing, kidney function, and how the drug moves from blood into tissues. For that reason, the sample is usually collected at a consistent point in your treatment and after the medication has had time to distribute, so the result reflects your typical level. Your clinician may order this test along with kidney and electrolyte tests.

Why it matters

Digoxin has a narrow safety window, which means the difference between an effective dose and a harmful dose is small. Too little may not control your condition, while too much can cause side effects affecting the heart, stomach, vision, and nervous system. Checking your level helps your clinician tailor the dose, identify drug interactions, and reduce the risk of toxicity.

This test is often ordered when starting therapy, after a dose change, when adding or stopping other medicines, if kidney function changes, in older adults, or when you have symptoms that could be related to digoxin effect such as nausea, decreased appetite, confusion, vision changes, or an irregular heartbeat.

Understanding your results

Your result is interpreted together with the time of your last dose, your symptoms, your heart rhythm, kidney function, and electrolyte levels. A value that looks higher or lower than expected can often be explained by sample timing or recent dosing changes, so your care team will consider the full picture.

If the level suggests excessive exposure and you have symptoms, your clinician may adjust or temporarily hold doses, review other medicines for interactions, obtain an electrocardiogram, and repeat labs. If it appears lower than intended, the plan may include adjusting the dose or timing, addressing interactions, and rechecking the level. Do not change or stop digoxin without medical advice.

Some situations can make results less reliable, such as soon after receiving digoxin immune antibody fragments for overdose or the presence of substances that cross react in certain assays. Tell your clinician about recent treatments, supplements, and pregnancy so they can interpret the result correctly.

Reference ranges

12.6 nmol/L
All sexes
0 days – 150 years

Reference intervals vary by laboratory, analyzer, methodology, population, and units. The ranges shown here are for education only. Always interpret your results against the reference interval printed on your own lab report.

Factors that could impact Digoxin

  • Timing of the blood draw

    Levels are most meaningful when the sample is collected at a consistent time in your dosing cycle and after the medication has had time to move from blood into tissues. Early sampling after a dose can appear falsely high.

  • Kidney function

    Your kidneys clear most digoxin. Reduced kidney function can raise blood levels and increase the risk of side effects, while improving kidney function or increased urine output can lower levels.

  • Drug interactions

    Medicines that affect P‑glycoprotein or kidney handling of digoxin can raise or lower levels. Examples include amiodarone, verapamil, diltiazem, macrolide antibiotics, azole antifungals, and rifampin. Always review new prescriptions and supplements with your clinician.

  • Electrolyte balance

    Low potassium or magnesium or high calcium can increase sensitivity to digoxin and the risk of heart rhythm problems even when the measured level is not markedly elevated.

  • Age, weight, and thyroid status

    Older age, low body weight, and thyroid disorders can change how your body handles digoxin, often requiring lower doses and closer monitoring.

  • Assay interference and special treatments

    After treatment with digoxin immune antibody fragments for overdose, many assays read artificially high. Endogenous substances in some people can also cross react with certain tests. Tell the lab and your clinician about recent treatments.

  • Adherence and dosing changes

    Missed or extra doses, changes in dose, or taking doses at irregular times can significantly change the measured level and its interpretation.

2026

References

  1. McGill University Health Centre. (2015, July 02). Digoxin (Task CD 685587). Laboratory reference ranges.
  2. Heidenreich, P. A., Bozkurt, B., Aguilar, D., Allen, L. A., Byun, J. J., Colvin, M. M., Deswal, A., Drazner, M. H., Dunlay, S. M., Evers, L. R., Fang, J. C., Fedson, S. E., Fonarow, G. C., Hayek, S. S., Hernandez, A. F., Khazanie, P., Kittleson, M. M., Lee, C. S., Link, M. S., ... Yancy, C. W. (2022). 2022 AHA/ACC/HFSA guideline for the management of heart failure. Journal of the American College of Cardiology, 79(17), e263–e421. External link
  3. January, C. T., Wann, L. S., Calkins, H., Chen, L. Y., Cigarroa, J. E., Cleveland, J. C., Ellinor, P. T., Ezekowitz, M. D., Field, M. E., Furie, K. L., Heidenreich, P. A., Murray, K. T., Shea, J. B., Tracy, C. M., & Yancy, C. W. (2019). 2019 AHA/ACC/HRS focused update of the 2014 guideline for the management of patients with atrial fibrillation. Circulation, 140(2), e125–e151. External link
  4. Specialist Pharmacy Service. (2023). Digoxin monitoring. SPS Medicines Advice. External link