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GLP-1 Blood Tests: What to Draw, and What Not To

5 min read · doses off DailyMed · last verified May 2026

By Ruth Calder · Enforcement Editor
Editorially reviewed (not clinically reviewed). Not medical advice · How we verify contentLast reviewed

There is a reasonable set of blood tests to have before starting one of these drugs, a much shorter list worth repeating, and a handful that get ordered routinely without supporting evidence. Few people leave the prescribing appointment with any of that written down.

Before the first dose

TestWhat it is for
HbA1cEstablishes where you are starting — normal, prediabetic or diabetic — and gives you something to measure response against.
Fasting glucoseFlags hypoglycemia risk if insulin or a sulfonylurea is already on board.
Lipid panelThese drugs move triglycerides, so a baseline lets you tell drug effect from everything else you changed at the same time.
Liver panelFatty liver disease is common in this population. Without a starting ALT and AST, a later number means very little.
Creatinine and eGFRThe most useful one on the list. Dehydration is the main kidney risk on these drugs, and you cannot detect a meaningful fall without knowing where you began.
TSHAn underactive thyroid looks exactly like resistance to weight loss. Worth excluding before blaming a plateau on the drug.
Vitamin B12, if you take metforminMetformin depletes B12 in a substantial minority of long-term users, and eating less compounds it.
Calcitonin — only with a family history of MTCNot a screening test. Without a nodule or a family history it produces far more confusion than information.

While you are titrating

Less than people expect. No label requires routine bloods during the climb.

  • Around week 4, a conversation rather than a blood test — how the nausea is, whether you are keeping fluids down, blood pressure, and whether fasting glucose is drifting low enough to warrant cutting the insulin or sulfonylurea.
  • Around week 12, repeat the A1C if you are treating diabetes. Three months should show movement; a flat result at an adequate dose is a prompt to ask why.
  • Liver tests only if something is wrong — new right-sided pain, yellowing, or nausea still going strong past the first month.
  • Repeat creatinine after any bad episode of vomiting or diarrhea, roughly a week or two afterwards. This is the recheck most worth remembering.
  • Pregnancy testing before each step up for anyone who could become pregnant — particularly given that tirzepatide's label flags reduced oral-contraceptive reliability for four weeks after every escalation.
  • Lipase only if pancreatitis is genuinely on the table — severe pain reaching through to the back. Not as a routine.

Once you are settled

  • A1C every three months until you are at target, then twice a year.
  • Lipids once a year, more often only around a statin change.
  • Liver panel once a year, more often with fatty liver disease or new symptoms.
  • Creatinine once a year — every three to six months if your eGFR is under 60, or you take an ACE inhibitor, an ARB or a diuretic.
  • TSH only if something suggests it. A normal baseline does not need repeating annually.
  • B12 every year or two alongside metformin, sooner with pins and needles or anemia.
  • Calcitonin: no routine repeat. The boxed warning is managed by counseling and examining your neck, not by surveillance bloods.

⛔ What not to order

This half gets left out of most guidance, and it costs people money and anxiety.

  • Lipase or amylase as a screen. In someone without symptoms the false-positive rate is high and a mildly raised result predicts very little. The labels direct testing when there are clinical signs — not before.
  • Calcitonin as a screen. Without a family history or a nodule it is not endorsed as surveillance by anyone.
  • Tumor markers — CEA, CA 19-9, CA 125. No indication whatsoever here. Ordering them generates expensive investigation of false positives.
  • Scheduled DEXA scans. Genuinely useful in research and in selected patients; not something everyone on a GLP-1 needs on a timetable.

Results that need acting on

  • ALT or AST more than three times the upper limit. Hold, repeat in a week or two, and look for other causes — alcohol, paracetamol, viral, other drugs.
  • Creatinine up more than about a quarter from baseline, or eGFR falling into a new band. Hold the dose, get fluids in, look again at NSAIDs and blood-pressure medication, then repeat the test.
  • Fasting glucose under 70, or any symptomatic hypo on insulin or a sulfonylurea. ★ The thing to reduce is the insulin or sulfonylurea — not the GLP-1.
  • Weight climbing or A1C rising at a steady dose. Before concluding the drug has stopped working, check the boring explanations: storage, missed doses, injection technique.
  • Lipase over three times the upper limit with pain radiating to the back. Stop, image, and do not restart until it is cleared.

What this does not cover

Type 1 diabetes monitoring, which is a different discipline and outside these drugs' approved use. Children, where the product labels add growth, puberty and mood screening. And bariatric protocols, which overlap only partly with this.

Where to go next

References

  1. 1.Lundgren JR, Janus C, Jensen SBK, et al. Healthy Weight Loss Maintenance with Exercise, Liraglutide, or Both Combined (S-LITE). N Engl J Med. 2021. PMID: 33951361.
  2. 2.U.S. National Library of Medicine — DailyMed. WEGOVY (semaglutide) — SPL. DailyMed. 2026. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ee06186f-2aa3-4990-a760-757579d8f77b
  3. 3.U.S. National Library of Medicine — DailyMed. ZEPBOUND (tirzepatide) — SPL. DailyMed. 2026. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=487cd7e7-434c-4925-99fa-aa80b1cc776b
  4. 4.Paluch AE, Bajpai S, Bassett DR, et al. Daily steps and all-cause mortality: a meta-analysis of 15 international cohorts. Lancet Public Health. 2022. PMID: 35247352.

Frequently Asked Questions

A sensible baseline runs to HbA1c, a fasting glucose, lipids, liver enzymes, creatinine with eGFR, and thyroid function — plus B12 if you also take metformin. The kidney measurement is the one that earns its place most clearly, because dehydration is the main renal risk on these drugs and a later result means nothing without a starting point. Calcitonin belongs on the list only if medullary thyroid carcinoma runs in your family.
Every three months until you reach your target, then twice a year. After a GLP-1 is added, many prescribers also take an earlier look at four to eight weeks using a fasting glucose or a continuous monitor, specifically to catch over-correction before the three-month reading arrives.
No to all three, and this is where over-testing does real harm. Lipase and amylase in someone without symptoms produce false positives at a high rate, and a mildly raised figure predicts very little — the labels direct testing when there are clinical signs. Calcitonin is not endorsed as surveillance without a family history or a thyroid nodule. Tumor markers have no place here at all.
Liver enzymes above three times the upper limit, a creatinine rise of more than roughly a quarter from baseline, or a lipase above three times the upper limit accompanied by pain boring through to the back. Symptomatic hypoglycemia also demands action — but there the correct move is reducing the insulin or sulfonylurea rather than the GLP-1, since the GLP-1 is rarely the component causing it.

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Editorial reference content, not medical advice. Changing a dose, holding one, or stopping altogether is a decision for you and your prescriber together. As for the numbers: we checked every dose figure here against the FDA-approved Structured Product Label on DailyMed in May 2026.

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