GLP-1 side effect rates, and why they cannot be compared
All four labels report nausea, vomiting, diarrhea and constipation. They report them in different populations, against different comparators, at different reporting thresholds and over different trial lengths — and every one of them prints a sentence saying the numbers must not be compared across drugs. The tables below are therefore reproduced separately, each with the conditions that produced it.
Reviewed by Ellis Brandt. Sources checked September 2026.
This guide draws on the cited FDA-approved prescribing information and other FDA sources. It is not medical advice; discuss treatment with your clinician. See the medical disclaimer.
Why these four tables are not one table
A reader who wants to know whether semaglutide or tirzepatide causes more nausea is asking a reasonable question that these documents do not answer. The two diabetes labels report rates in patients with type 2 diabetes at a threshold of 5%; the two weight labels report rates in patients with obesity or overweight at a threshold of 2% and greater than placebo. A 44% in one table and an 18% in another describe different people, different doses and different counting rules.
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| Label | Population in the table | Reporting threshold | Comparator arm |
|---|---|---|---|
| Ozempic | Adults with type 2 diabetes mellitus, placebo-controlled trials | Reported in at least 5% of Ozempic-treated patients | Placebo, N=262 |
| Wegovy | Adults with obesity or overweight, for weight reduction | At least 2% and greater than placebo | Placebo, N=1,261 |
| Mounjaro | Adults with type 2 diabetes mellitus, pool of placebo-controlled trials | Reported in at least 5% of Mounjaro-treated patients | Placebo, N=235 |
| Zepbound | Adults with obesity or overweight, weight reduction and long-term maintenance trials (Study 1 and Study 2) | At least 2% and greater than placebo | Placebo, N=958 |
Ozempic
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| Adverse reaction | Placebo (N=262) % | Ozempic 0.5 mg (N=260) % | Ozempic 1 mg (N=261) % |
|---|---|---|---|
| Nausea | 6.1 | 15.8 | 20.3 |
| Vomiting | 2.3 | 5 | 9.2 |
| Diarrhea | 1.9 | 8.5 | 8.8 |
| Abdominal pain | 4.6 | 7.3 | 5.7 |
| Constipation | 1.5 | 5 | 3.1 |
The same section reports gastrointestinal adverse reactions overall at placebo 15.3%, Ozempic 0.5 mg 32.7% and Ozempic 1 mg 36.4%, and states that “the majority of reports of nausea, vomiting, and/or diarrhea occurred during dose escalation.” Discontinuation because of a gastrointestinal reaction: 0.4% on placebo, 3.1% on 0.5 mg, 3.8% on 1 mg.
Percent of patients in each arm of the label's pooled placebo-controlled trials. The track is 100% of the arm, so the unfilled part of each bar is the share who reported none.
Ozempic prescribing information, section 6.1, “Gastrointestinal Adverse Reactions”, in the pool of placebo-controlled trials. Label version 20, effective 2026-06-01, read September 2026. These are one label’s numbers and are not comparable to any other label’s — that is what the sentence at the top of this page says, and it is why this figure draws three arms of one trial rather than four drugs.
Wegovy
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| Adverse reaction | Placebo (N=1,261) % | Wegovy injection 2.4 mg once weekly (N=2,116) % |
|---|---|---|
| Nausea | 16 | 44 |
| Diarrhea | 16 | 30 |
| Vomiting | 6 | 24 |
| Constipation | 11 | 24 |
| Abdominal pain | 10 | 20 |
| Headache | 10 | 14 |
| Fatigue | 5 | 11 |
| Dyspepsia | 3 | 9 |
| Dizziness | 4 | 8 |
| Hair loss | 1 | 3 |
Ten rows of a longer table, chosen as the ones a reader asks about; the label’s own table runs to nineteen. The fatigue and hair loss rows are broken out by dose and by sex on fatigue and hair loss. In these trials 6.8% of patients on Wegovy 2.4 mg and 3.2% on placebo permanently discontinued because of an adverse reaction — most often nausea (1.8% against 0.2%), vomiting (1.2% against 0%) and diarrhea (0.7% against 0.1%).
The label carries a second table for the 7.2 mg dosage, against both placebo and 2.4 mg. There, nausea is 13% on placebo, 35% on 2.4 mg and 39% on 7.2 mg, and dysesthesia — an abnormal sensation — is 0%, 6% and 22%.
Mounjaro
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| Adverse reaction | Placebo (N=235) % | 5 mg (N=237) % | 10 mg (N=240) % | 15 mg (N=241) % |
|---|---|---|---|---|
| Nausea | 4 | 12 | 15 | 18 |
| Diarrhea | 9 | 12 | 13 | 17 |
| Decreased appetite | 1 | 5 | 10 | 11 |
| Vomiting | 2 | 5 | 5 | 9 |
| Constipation | 1 | 6 | 6 | 7 |
| Dyspepsia | 3 | 8 | 8 | 5 |
| Abdominal pain | 4 | 6 | 5 | 5 |
Zepbound
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| Adverse reaction | Placebo (N=958) % | 5 mg (N=630) % | 10 mg (N=948) % | 15 mg (N=941) % |
|---|---|---|---|---|
| Nausea | 8 | 25 | 29 | 28 |
| Diarrhea | 8 | 19 | 21 | 23 |
| Vomiting | 2 | 8 | 11 | 13 |
| Constipation | 5 | 17 | 14 | 11 |
| Abdominal pain | 5 | 9 | 9 | 10 |
| Dyspepsia | 4 | 9 | 9 | 10 |
| Injection site reactions | 2 | 6 | 8 | 8 |
| Hair loss | 1 | 5 | 4 | 5 |
Eight rows of a sixteen-row table. The label ties its hair loss row to weight reduction, and it was reported mostly by women. The Zepbound label also quantifies the severe end: in a pool of two weight-reduction trials, severe gastrointestinal adverse reactions were reported in 1% on placebo, 1.7% on 5 mg, 2.5% on 10 mg and 3.1% on 15 mg. The same section states that Zepbound “is not recommended in patients with severe gastroparesis.”
What none of these tables tells you
They are trial rates, and every label says so itself, once, in the sentence quoted at the top of this page — the phrase “may not reflect the rates observed in practice” is the tail of that same sentence, not a second warning. Counted in each document: it occurs exactly once on each of the four. They describe selected populations followed for a fixed period under supervision, and they are the best-quality numbers that exist for these products. They are not a forecast for any individual, and nothing here turns them into one.
They also say nothing about compounded semaglutide or compounded tirzepatide, which have no approved label and no trial tables of their own. Related: the dose escalation schedules, which is where each label locates most of these reactions.
Sources
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| Label | Applicant on the label | SPL version | Label effective date | Where it was read |
|---|---|---|---|---|
| Ozempic (semaglutide) | Novo Nordisk Pharmaceutical Industries, LP | 20 | 2026-06-01 | DailyMed, set id adec4fd2-6858-4c99-91d4-531f5f2a2d79 |
| Wegovy (semaglutide) | Novo Nordisk Pharmaceutical Industries, LP | 19 | 2026-06-18 | DailyMed, set id ee06186f-2aa3-4990-a760-757579d8f77b |
| Mounjaro (tirzepatide) | Eli Lilly and Company | 40 | 2026-08-27 | DailyMed, set id d2d7da5d-ad07-4228-955f-cf7e355c8cc0 |
| Zepbound (tirzepatide) | Eli Lilly and Company | 40 | 2026-08-28 | DailyMed, set id 487cd7e7-434c-4925-99fa-aa80b1cc776b |
The rates are from the adverse-reaction tables in section 6.1 of each label. Every figure and quotation comes from the label’s own tables and text. Each label is the FDA-approved version that was current when it was read in September 2026, identified in the table by its version number and effective date.
See the providers
Side effects are a property of the drug, not the seller. The boards list who sells it and what each one publishes.
- Semaglutide providersprovider board
Compare semaglutide plans, pharmacy details and cancellation terms.
- Tirzepatide providersprovider board
Compare tirzepatide plans, pharmacy details and cancellation terms.
More, read from the same labels
- First-year GLP-1 costsresearch guide
A low monthly headline does not tell you what a year of treatment will cost. Compare the same medication and service package, then separate the total you expect to spend from the amount you must pay before treatment begins.
- Cancellation and refundsresearch guide
Canceling future membership charges, stopping an upcoming medication order and requesting a refund are three different requests. Get a written answer for each one that applies to you.
- Insurance denial documentsresearch guide
The next step depends on why coverage was denied. A missing document, a formulary restriction and an excluded benefit are different problems. Start with the written decision before paying someone to submit another request.
- Savings and cash-pay eligibilityresearch guide
A manufacturer savings card and a self-pay offer can have different eligibility rules, even for the same medicine. Match the offer to your coverage and exact product before using its advertised price in your budget.
- Verify your GLP-1 pharmacyresearch guide
The website taking your payment, the clinician prescribing and the pharmacy dispensing may be different businesses. Identify each one. A recognizable brand or a reassuring badge does not tell you who will fill the prescription.
- Changing GLP-1 providersresearch guide
Before ending your current service, establish what the new practice needs, what it will charge and when it can evaluate you. Transferring your records does not guarantee that another clinician will continue the same prescription.
- Weight regain after stoppingresearch guide
Weight regain occurred after treatment withdrawal in studies of semaglutide and tirzepatide. The findings support planning follow-up and affordability before an interruption, but they do not predict exactly what will happen to one person.
- Semaglutide vs tirzepatideresearch guide
What the four FDA-approved labels say each molecule is, what each is approved to treat, and where the two differ.
- How they workresearch guide
The receptor each molecule switches on, what the labels say that does to appetite, blood sugar and the stomach, and why one dose lasts a week.
- Is Ozempic insulin?research guide
What the Ozempic label calls semaglutide, how that differs from insulin, and where insulin appears on these labels as a separate medicine.
- Zepbound vs Ozempicresearch guide
Four brand names, two molecules and two kinds of approval: which of these products are the same drug, and what each one is actually approved to do.
- Dose escalation schedulesresearch guide
The starting dose, the escalation interval and the maximum dose each label sets, and why they are not interchangeable.
- Hair lossresearch guide
Which labels report hair loss, the rate against placebo where a trial measured it, and why two of them put no number on it.
- Fatigue and tirednessresearch guide
Which labels list fatigue, the rate against placebo where a trial measured it, and what each label counts as fatigue.
- Missed dose rulesresearch guide
The window each label gives for a late dose, and the minimum gap it requires when the injection day changes.
- Drug interactionsresearch guide
Insulin and sulfonylureas, oral medications, and the oral-contraceptive precaution that appears on two of these four labels and not the other two.
- Buying one onlineresearch guide
The agency's own warning signs for a telehealth GLP-1 seller, its 28-day vial rule, and what it says about drugs that arrive warm.
- Zepbound by doseresearch guide
What each Zepbound dose achieved in the trials printed in its label, what the label says about choosing a maintenance dose, and what the higher doses cost in side effects.
- Zepbound at 3 monthsresearch guide
What does the Zepbound label report about three-month weight loss and maintenance dosing?
- Injecting tirzepatideresearch guide
The injection sites, the rotation rule and the steps for the single-dose pen, the KwikPen and the vial and syringe, exactly as the FDA-approved Instructions for Use give them.
- Refrigeration and storageresearch guide
How cold each pen is kept, how many days it can spend at room temperature, and what the labels say about heat and freezing.
- Who should not take oneresearch guide
The boxed warning every one of these labels carries, the two contraindications, and which warnings appear on which product.
The sentence on every label
“Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.”
Printed at the head of section 6.1 on Ozempic, Mounjaro and Zepbound, read September 2026. Wegovy prints the same sentence with one word changed — “…cannot be directly compared to rates in the clinical studies of another drug”.