GLP-1 washout / clearance calculator

How long does a GLP-1 stay in your system?

Pick your GLP-1 and see how long after your last dose the drug level drops to 50%, 25%, 10%, 5%, 1%, and 0.1% of peak. Built on the FDA-label elimination half-lives — semaglutide ~7 days, tirzepatide ~5 days, orforglipron ~36 hours, retatrutide ~6 days. Includes clinical scenarios for switching between GLP-1s, pre-surgery hold, pregnancy planning, and clinical trial enrollment.

Pick your GLP-1

Elimination half-life

7.0 days

168 hours

Dosing interval

Weekly

Once per 7 days

Source

FDA prescribing information + published PK literature

Drug concentration after your last dose

Population-mean exponential decay starting from your final steady-state peak. The curve does not account for individual variation in clearance.

100%50%25%10%5%1%0d7d14d30d60d90d

Time to each residual concentration

How long after your last dose until the drug level drops to each fraction of its peak.

50% of peak

7 days

7.0 days after last dose

25% of peak

14 days

14.0 days after last dose

10% of peak

23 days

23.3 days after last dose

5% of peak

30 days

30.3 days after last dose

1% of peak

46 days

46.5 days after last dose

0.1% of peak

69 days

69.8 days after last dose

Clinical scenarios

Common reasons patients ask “how long does it stay in my system” — with the standard practice for each.

Switching to another GLP-1

Standard practice is to start the new GLP-1 at its lowest titration step on the next scheduled injection day after the last dose of the prior drug. No biological washout is required.

7 days

~50.00% remaining

Source: FDA Wegovy/Ozempic/Zepbound/Mounjaro PI; common clinical practice

Pre-surgery hold (weight management indication)

ASA 2023 guidance: hold weekly GLP-1s for 1 week before any general anesthesia or deep sedation procedure. The 2024 multi-society update adds a 24-hour clear-liquid diet on top.

7 days

~50.00% remaining

Source: ASA Consensus Statement 2023; ASA/AGA/ASMBS 2024 update

Conventional clinical washout (5 half-lives)

After 5 half-lives, approximately 97% of the drug has cleared. This is the standard pharmacology textbook definition of 'washed out' and is commonly used as the cutoff for crossover trial designs and clinical studies.

35 days

~3.13% remaining

Source: Standard pharmacokinetic principle (Goodman & Gilman)

Pregnancy planning (Wegovy label)

The Wegovy prescribing information recommends discontinuing semaglutide at least 2 months before a planned pregnancy because of the long half-life and limited human pregnancy data. Apply the same 2-month rule for tirzepatide and other long-half-life GLP-1s.

60 days

~0.26% remaining

Source: Wegovy PI Section 8.1; analogous practice for tirzepatide

Research-grade washout (10 half-lives)

After 10 half-lives, approximately 99.9% of the drug has cleared. This is the threshold used by some clinical trials to declare a patient drug-free for enrollment in another GLP-1 study.

70 days

~0.10% remaining

Source: Standard pharmacokinetic principle

Important caveats. These calculations use the population-mean half-life from the FDA prescribing information. Individual half-lives can vary by ±30% based on body composition, kidney function, and how long you were on a stable maintenance dose before stopping. The pharmacologic effect (gastric emptying, satiety) often outlasts the blood concentration. Do not use this tool to make medical decisions without confirming with your prescriber.

The math, explained

GLP-1 receptor agonists clear from the body via first-order elimination kinetics, which means a fixed fraction of the drug is eliminated per unit time rather than a fixed amount. The result is exponential decay: after one half-life, 50% of the peak concentration remains; after two half-lives, 25%; after three, 12.5%; and so on. The formula is:

C(t) = C_peak × 0.5^(t / t_half)

The half-life values used by this calculator come from the FDA prescribing information and the published clinical pharmacology literature [1][2][3][4][5]:

  • Semaglutide — 7 days (168 hours). Sourced from the Wegovy and Ozempic prescribing information and the Hall 2018 PK review[4].
  • Tirzepatide — 5 days (120 hours). Sourced from the Zepbound and Mounjaro prescribing information and Urva 2021[5].
  • Orforglipron — ~36 hours. The newer non-peptide oral GLP-1 has a much shorter half-life than the injectable peptides.
  • Retatrutide — ~6 days (144 hours), per the published phase 2 obesity trial.

The clinical milestones the calculator reports

  • Switching to another GLP-1. No biological washout is required — start the new drug at its lowest titration step on the next scheduled injection day. See our switching guide for the dose mapping and protocol.
  • Pre-surgery hold. The American Society of Anesthesiologists 2023 statement and the 2024 multi-society update[6] recommend holding weekly GLP-1s for 1 week before any procedure under general anesthesia or deep sedation. See our ASA guidance article for the full protocol.
  • Pregnancy planning. The Wegovy prescribing information recommends discontinuing semaglutide at least 2 months before a planned pregnancy because of the long half-life and limited human pregnancy data. The same 2-month rule is generally applied to tirzepatide. Foundayo (orforglipron) has a shorter washout because of its 36-hour half-life. See our pregnancy and fertility guide for the full obstetric guidance.
  • 5 half-lives ≈ 97% cleared. The standard pharmacology textbook definition of “washed out.” Used as the cutoff for many crossover trial designs.
  • 10 half-lives ≈ 99.9% cleared. The research-grade washout used by some clinical trials to declare a patient drug-free for enrollment in a different GLP-1 study.

Important caveats

  • Population means, not your half-life. Individual half-lives vary by ±30% based on body composition, kidney function, and the steady-state context. Patients with reduced kidney function may clear semaglutide and tirzepatide more slowly.
  • Steady state vs partial titration. The calculator assumes you were on a stable maintenance dose for at least 5 half-lives before stopping. Patients who stopped during titration have lower starting concentrations and clear faster.
  • Effect outlasts blood level. Gastric emptying delay, satiety, and weight-loss effects often persist for days or weeks after blood levels become negligible. Washout of the drug is NOT the same as washout of the clinical effect.
  • No standardized assay. “Undetectable” depends entirely on which assay you use. There is no routine clinical lab for semaglutide or tirzepatide blood levels — the “0.1%” milestone is a research/PK concept, not a clinical lab result you can order.

What this is NOT

This is an educational calculator built on standard pharmacokinetic principles and FDA-label half-life values. It is not a substitute for clinical judgment. If you need to make a real decision about stopping a GLP-1 — for surgery, pregnancy, switching drugs, or any other reason — confirm the timing with your prescribing clinician and (for surgery) with your anesthesia team.

Related tools and research

Important disclaimer

This tool is for educational purposes only and does not constitute medical advice. The calculator uses population-mean half-lives from the FDA prescribing information, and individual values vary substantially. Always discuss any decision to stop, hold, or restart a GLP-1 with your prescribing clinician.

References

  1. 1.Novo Nordisk Inc. WEGOVY (semaglutide) injection — US Prescribing Information, Section 12.3 Pharmacokinetics (elimination half-life ~7 days). FDA Approved Labeling. 2025. https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/215256s024lbl.pdf
  2. 2.Eli Lilly and Company. ZEPBOUND (tirzepatide) injection — US Prescribing Information, Section 12.3 Pharmacokinetics (elimination half-life ~5 days). FDA Approved Labeling. 2025. https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/217806s016lbl.pdf
  3. 3.Eli Lilly and Company. FOUNDAYO (orforglipron) tablets — US Prescribing Information. FDA Approved Labeling. 2026. https://investor.lilly.com/news-releases/news-release-details/fda-approves-lillys-foundayotm-orforglipron-only-glp-1-pill
  4. 4.Hall S, Isaacs D, Clements JN. Pharmacokinetics and Clinical Implications of Semaglutide: A New Glucagon-Like Peptide (GLP)-1 Receptor Agonist. Clin Pharmacokinet. 2018. PMID: 29915923.
  5. 5.Urva S, Quinlan T, Landry J, Martin J, Loghin C. Effects of Renal Impairment on the Pharmacokinetics of the Dual GLP-1 and GIP Receptor Agonist Tirzepatide. Clin Pharmacokinet. 2021. PMID: 33704694.
  6. 6.American Society of Anesthesiologists, American Gastroenterological Association, American Society for Metabolic and Bariatric Surgery, International Society of Perioperative Care of Patients with Obesity, Society of American Gastrointestinal and Endoscopic Surgeons. Multisociety Clinical Practice Guidance for the Safe Use of GLP-1 Receptor Agonists in the Perioperative Period. ASA / AGA / ASMBS / IPSO / SAGES Joint Statement. 2024. https://www.asahq.org/about-asa/newsroom/news-releases/2024/10/multisociety-clinical-practice-guidance-for-the-safe-use-of-glp-1s