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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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4 adverse-reaction tables and the conditions that produced them — read September 2026
LabelPopulation in the tableReporting thresholdComparator arm
OzempicAdults with type 2 diabetes mellitus, placebo-controlled trialsReported in at least 5% of Ozempic-treated patientsPlacebo, N=262
WegovyAdults with obesity or overweight, for weight reductionAt least 2% and greater than placeboPlacebo, N=1,261
MounjaroAdults with type 2 diabetes mellitus, pool of placebo-controlled trialsReported in at least 5% of Mounjaro-treated patientsPlacebo, N=235
ZepboundAdults with obesity or overweight, weight reduction and long-term maintenance trials (Study 1 and Study 2)At least 2% and greater than placeboPlacebo, N=958

Ozempic

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Ozempic, adverse reactions in ≥5% of treated patients with type 2 diabetes — label version 20, effective 2026-06-01
Adverse reactionPlacebo (N=262) %Ozempic 0.5 mg (N=260) %Ozempic 1 mg (N=261) %
Nausea6.115.820.3
Vomiting2.359.2
Diarrhea1.98.58.8
Abdominal pain4.67.35.7
Constipation1.553.1

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.

Any gastrointestinal adverse reaction, by treatment arm — Ozempic label version 20, effective 2026-06-01

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.

  1. Placebo

    15.3%

  2. Ozempic 0.5 mg once weekly

    32.7%

  3. Ozempic 1 mg once weekly

    36.4%

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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Wegovy injection 2.4 mg, adverse reactions ≥2% and greater than placebo in adults with obesity or overweight — label version 19, effective 2026-06-18
Adverse reactionPlacebo (N=1,261) %Wegovy injection 2.4 mg once weekly (N=2,116) %
Nausea1644
Diarrhea1630
Vomiting624
Constipation1124
Abdominal pain1020
Headache1014
Fatigue511
Dyspepsia39
Dizziness48
Hair loss13

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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Mounjaro, adverse reactions in ≥5% of treated adults with type 2 diabetes — label version 40, effective 2026-08-27
Adverse reactionPlacebo (N=235) %5 mg (N=237) %10 mg (N=240) %15 mg (N=241) %
Nausea4121518
Diarrhea9121317
Decreased appetite151011
Vomiting2559
Constipation1667
Dyspepsia3885
Abdominal pain4655

Zepbound

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Zepbound, adverse reactions ≥2% and greater than placebo in adults with obesity or overweight — label version 40, effective 2026-08-28
Adverse reactionPlacebo (N=958) %5 mg (N=630) %10 mg (N=948) %15 mg (N=941) %
Nausea8252928
Diarrhea8192123
Vomiting281113
Constipation5171411
Abdominal pain59910
Dyspepsia49910
Injection site reactions2688
Hair loss1545

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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Sources: 4 FDA-approved labels, read September 2026
LabelApplicant on the labelSPL versionLabel effective dateWhere it was read
Ozempic (semaglutide)Novo Nordisk Pharmaceutical Industries, LP202026-06-01DailyMed, set id adec4fd2-6858-4c99-91d4-531f5f2a2d79
Wegovy (semaglutide)Novo Nordisk Pharmaceutical Industries, LP192026-06-18DailyMed, set id ee06186f-2aa3-4990-a760-757579d8f77b
Mounjaro (tirzepatide)Eli Lilly and Company402026-08-27DailyMed, set id d2d7da5d-ad07-4228-955f-cf7e355c8cc0
Zepbound (tirzepatide)Eli Lilly and Company402026-08-28DailyMed, 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.

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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”.

About our comparisons. Our scores measure published information, not medical quality. We do not assign an overall provider rating or rank providers by treatment outcomes.