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Symptom question · incretin class
Does a GLP-1 cause burping?
None of the 36 compound guides checked lists burping as a reported side effect. 25 have published safety information that does not mention it. BPC-157, TB-500, GHK-Cu, MOTS-c, Epitalon, Kisspeptin-10, IGF-1 LR3, PEG-MGF, KPV, Selank and AHK-Cu have no published human safety data.
Source: checked against 36 compound guides; rates are shown exactly as reportedFDA label
FDA data lists belching among the twenty-five most-reported terms for two of eight brands, and both contain tirzepatide. For the other six, the term falls below each product’s cut-off; that does not mean zero reports.
The two sources disagree because they measure different things. A side effect may be absent from a label summary yet common in reports filed after a product reaches the market.
Information checked 2026-08-20
At a glance
Compounds that list it
0 of 36
Only in a combined category
0
No published human safety data
11
Best available source
FDA label
Which compounds list burping
None of the labels or trials checked lists burping as a reported side effect. FDA reports filed after the medicines went on sale tell a different story, so those results appear in a separate table below.
| Compound | How it appears | Frequency reported | Source type |
|---|---|---|---|
| TirzepatideZepbound, Mounjaro | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | FDA label |
| SemaglutideWegovy, Ozempic, Rybelsus | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | FDA label |
| LiraglutideVictoza, Saxenda | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | FDA label |
| Retatrutide | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | Human trial |
| Cagrilintide | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | Human trial |
| Survodutide | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | Human trial |
| BPC-157 | No published human safety dataNo human trial has published enough safety data to list reactions for this compound. | — | no human dose shown to work |
| TesamorelinEgrifta SV, Egrifta WR | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | FDA label |
| PT-141Vyleesi | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | FDA label |
| CJC-1295 | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | limited human data |
| Ipamorelin | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | Human trial |
| TB-500 | No published human safety dataNo human trial has published enough safety data to list reactions for this compound. | — | no human dose shown to work |
| GHK-Cu | No published human safety dataNo human trial has published enough safety data to list reactions for this compound. | — | no human dose shown to work |
| Sermorelin | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | limited human data |
| MOTS-c | No published human safety dataNo human trial has published enough safety data to list reactions for this compound. | — | no human dose shown to work |
| AOD-9604 | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | limited human data |
| NAD+ | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | limited human data |
| Epitalon | No published human safety dataNo human trial has published enough safety data to list reactions for this compound. | — | no human dose shown to work |
| Kisspeptin-10 | No published human safety dataNo human trial has published enough safety data to list reactions for this compound. | — | no human dose shown to work |
| DSIP | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | limited human data |
| Hexarelin | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | limited human data |
| IGF-1 LR3 | No published human safety dataNo human trial has published enough safety data to list reactions for this compound. | — | no human dose shown to work |
| PEG-MGF | No published human safety dataNo human trial has published enough safety data to list reactions for this compound. | — | no human dose shown to work |
| LL-37 | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | limited human data |
| KPV | No published human safety dataNo human trial has published enough safety data to list reactions for this compound. | — | no human dose shown to work |
| Thymosin alpha-1 | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | limited human data |
| SS-31Forzinity | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | FDA label |
| Semax | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | limited human data |
| Selank | No published human safety dataNo human trial has published enough safety data to list reactions for this compound. | — | no human dose shown to work |
| Melanotan II | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | limited human data |
| Mazdutide | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | Human trial |
| Pinealon | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | limited human data |
| AHK-Cu | No published human safety dataNo human trial has published enough safety data to list reactions for this compound. | — | no human dose shown to work |
| VK2735 | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | Human trial |
| Zenagamtide | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | Human trial |
| Pemvidutide | Not listed in the source checkedThe label or study checked for this compound does not list this reaction. | — | Human trial |
What people reported to the FDA
The first table summarizes labels and published trials. This table shows reports filed with the FDA after the medicines went on sale. Each percentage is the share of reports for that product that mention this symptom—not the share of patients who experienced it.
| Product | Share of its own reports | All reports |
|---|---|---|
| Ozempicsemaglutide | below 2.3% of Ozempic reports | 66,161 reports |
| Trulicitydulaglutide | below 2.1% of Trulicity reports | 88,332 reports |
| Rybelsussemaglutide | below 2.1% of Rybelsus reports | 7,379 reports |
| Wegovysemaglutide | below 2.0% of Wegovy reports | 21,044 reports |
| Zepboundtirzepatide | 1.9% of Zepbound reports | 70,141 reports |
| Saxendaliraglutide | below 1.9% of Saxenda reports | 10,040 reports |
| Mounjarotirzepatide | 1.7% of Mounjaro reports | 93,975 reports |
| Victozaliraglutide | below 1.7% of Victoza reports | 44,086 reports |
3Read deeper
Why the question is nearly always about sulfur
The searches behind this page rarely say burping on its own. They say sulfur burps, or egg burps, and they name a tirzepatide brand while doing it. That is a specific enough complaint that it is worth stating plainly what this site can and cannot do with it.
FDA files these reports under the general MedDRA term for belching. Smell is not recorded, so the data cannot confirm or rule out the sulfur description.
The general belching term appears for the two tirzepatide brands, while the stomach-emptying term appears for semaglutide products. Both findings come from the same FDA reporting system.
Why the label side is empty rather than negative
A blank row means the source we reviewed did not list burping. It does not prove the effect never happens or that no other document mentions it. Trial reports and label summaries do not reproduce every event in full.
This page is the clearest case in the section for why that distinction is kept. If an absence were published as a negative finding, this page would say these compounds do not cause burping — while the other document on the same page shows it among the most-filed complaints about two of them. The absence is about the extract, not about the world.
What this page does and does not establish
This is a page with a real finding and a small one, and the distance between those is where pages on this question usually go wrong.
| The claim | What the evidence shows |
|---|---|
| Both measured rows are tirzepatide products. | Established for those two brands. Zepbound and Mounjaro carry the term among their stored twenty-five; the other six sit below their own ceilings. |
| Tirzepatide causes more burping than semaglutide. | Not established. A share of reports is not a rate, and report volume tracks how long a product has been sold, how it is marketed and what people have been told to expect, as well as biology. |
| The six dashed rows mean those brands do not cause it. | Not established, and the row does not say that. It says the term sits at or below that product’s twenty-fifth most-reported, which is a ceiling, not a zero. |
| The reports confirm the sulfur description. | Not supported either way. FDA records belching under one general term and does not record smell. |
| No label lists burping. | Overstated. None of the extracted label or trial summaries lists it. Check the complete prescribing label for a specific product. |
Taking this to a clinician
Belching on its own is a nuisance rather than a warning sign, and nothing on this page suggests otherwise.
Common questions
Are sulfur burps a listed side effect of Zepbound or Mounjaro?
Not in the tirzepatide side-effect summary used for both brands.
FDA adverse-event data includes the general belching term for both brands but records nothing about smell, so it cannot answer the sulfur part specifically.
Why do the two measured rows matter if the numbers are small?
Because which products carry a term is a separate question from how large the share is, and it is the one this table can answer more confidently.
Both measured rows involve tirzepatide, but report counts cannot prove that the pattern is caused by the drug’s biology.
Is this the same as the gastroparesis question?
It is the same instrument read for a different term, and it comes out the other way round.
The stomach-emptying term appears with semaglutide products, while belching appears with tirzepatide products. Because both come from voluntary FDA reports, neither split proves a property of the molecule.
What would actually answer this?
A trial that recorded belching as an outcome, in a defined population, against a comparison group not taking the compound.
No source cited on this page is that. Until one exists, what this site can offer is the two documents it holds, kept apart, with what each one is stated on it.
The full profile for each compound
Want the full picture for one compound? Open its guide for uses, dosage information, side effects and serious warnings.
Tirzepatide reactions in full, including burping
What else semaglutide lists besides burping
Constipation read the same way as burping
Nausea across every page, as with burping
All source-checked pages, not only those listing burping
The burping question, asked about duration
Vial, water and draw for the burping compounds
Where burping sits among the symptom questions
The whole tirzepatide page, not just burping
- Zepbound (tirzepatide) — FDA-approved Prescribing Informationretrieved 2026-07-22FDA label
- Wegovy (semaglutide) — FDA-approved Prescribing Information (DailyMed)retrieved 2026-08-20FDA label
- Saxenda (liraglutide) injection — FDA-approved Prescribing Information (DailyMed)retrieved 2026-08-15FDA label
- Victoza (liraglutide) injection — FDA-approved Prescribing Information (DailyMed)retrieved 2026-08-15FDA label
- Jastreboff AM et al. Triple-Hormone-Receptor Agonist Retatrutide for Obesity — A Phase 2 Trial. N Engl J Med 2023;389:514-26 (PMID 37366315)retrieved 2026-08-12Human trial
- Lau DCW et al. Once-weekly cagrilintide for weight management: dose-finding phase 2 trial. Lancet 2021;398:2160-72 (PMID 34798060)retrieved 2026-08-17Human trial
- le Roux CW et al. Glucagon and GLP-1 receptor dual agonist survodutide for obesity: dose-finding phase 2 trial. Lancet Diabetes Endocrinol 2024 (PMID 38330987)retrieved 2026-08-20Human trial
- EGRIFTA SV (tesamorelin) for injection — FDA-approved Prescribing Information (DailyMed SPL)retrieved 2026-08-12FDA label
- EGRIFTA WR (tesamorelin) for injection — FDA-approved Prescribing Information (DailyMed SPL)retrieved 2026-08-12FDA label
- VYLEESI (bremelanotide) injection — FDA-approved Prescribing Information (DailyMed SPL)retrieved 2026-08-12FDA label
- Teichman SL, Neale A, Lawrence B, Gagnon C, Castaigne JP, Frohman LA. Prolonged stimulation of growth hormone (GH) and insulin-like growth factor I secretion by CJC-1295, a long-acting analog of GH-releasing hormone, in healthy adults. J Clin Endocrinol Metab 2006;91(3):799-805retrieved 2026-08-12Human trial
- Ionescu M, Frohman LA. Pulsatile secretion of growth hormone (GH) persists during continuous stimulation by CJC-1295, a long-acting GH-releasing hormone analog. J Clin Endocrinol Metab 2006;91(12):4792-7retrieved 2026-08-12Human trial
- Dominikowski A, Rękoś Z, Olejarz M, Szczepanek-Parulska E, Domin R, Ruchała M. The emerging landscape of performance-enhancing peptides modulating GH-IGF1 axis: bridging the gap between clinical evidence and patient self-administration. Front Endocrinol 2026;17 — Table 1, CJC-1295 (with DAC) safety-signal rowretrieved 2026-08-12limited human data
- Beck DE, Sweeney WB, McCarter MD; Ipamorelin 201 Study Group. Prospective, randomized, controlled, proof-of-concept study of the ghrelin mimetic ipamorelin for the management of postoperative ileus in bowel resection patients. Int J Colorectal Dis 2014;29(12):1527-34retrieved 2026-08-12Human trial
- Lanes R, Carrillo E; Venezuelan Collaborative Study Group. Long-term therapy with a single daily subcutaneous dose of growth hormone releasing hormone (1-29) in prepubertal growth hormone deficient children. J Pediatr Endocrinol 1994;7(4):303-8retrieved 2026-08-12Human trial
- Corpas E, Harman SM, Piñeyro MA, Roberson R, Blackman MR. Growth hormone (GH)-releasing hormone-(1-29) twice daily reverses the decreased GH and insulin-like growth factor-I levels in old men. J Clin Endocrinol Metab 1992;75(2):530-5retrieved 2026-08-12Human trial
- Reyna K, et al. Intravenous infusion of nicotinamide adenine dinucleotide (NAD+) versus nicotinamide riboside (NR): a retrospective tolerability pilot study in a real-world setting. Front Aging 2026;7:1652582retrieved 2026-08-12limited human data
- Dick P, Costa C, Fayolle K, et al. DSIP in the treatment of withdrawal syndromes from alcohol and opiates. Eur Neurol. 1984;23(3):188-93retrieved 2026-08-12limited human data
- Massoud AF, Hindmarsh PC, Brook CG. Hexarelin-induced growth hormone, cortisol, and prolactin release: a dose-response study. J Clin Endocrinol Metab 1996;81(12):4338-41retrieved 2026-08-12Human trial
- Rahim A, O’Neill PA, Shalet SM. Growth hormone status during long-term hexarelin therapy. J Clin Endocrinol Metab 1998;83(5):1644-9retrieved 2026-08-12Human trial
- Maccario M, Veldhuis JD, Broglio F, Di Vito L, Arvat E, Deghenghi R, Ghigo E. Impact of two or three daily subcutaneous injections of hexarelin, a synthetic growth hormone (GH) secretagogue, on 24-h GH, prolactin, adrenocorticotropin and cortisol secretion in humans. Eur J Endocrinol 2002;146(3):310-8retrieved 2026-08-12Human trial
- Induction of Antitumor Response in Melanoma Patients Using the Antimicrobial Peptide LL37 (NCT02225366) — MD Anderson Cancer Center, phase 1/2, completed, results postedretrieved 2026-08-12Human trial
- Dermatologic toxicity from novel therapy using antimicrobial peptide LL-37 in melanoma: a detailed examination of the clinicopathologic features (Journal of Cutaneous Pathology, 2018)retrieved 2026-08-12limited human data
- Wu J, et al. The efficacy and safety of thymosin alpha1 for sepsis (TESTS): multicentre, double blinded, randomised, placebo controlled, phase 3 trial. BMJ 2025;388:e082583retrieved 2026-08-12Human trial
- Wu J, et al. The efficacy of thymosin alpha 1 for severe sepsis (ETASS): a multicenter, single-blind, randomized and controlled trial. Crit Care 2013;17(1):R8retrieved 2026-08-12Human trial
- FORZINITY (elamipretide) injection, for subcutaneous use — FDA prescribing information, Stealth BioTherapeutics Inc., initial U.S. approval 2025 (NDA 215244). Source for the accelerated approval, the Barth syndrome indication, the 40 mg once-daily dose, the 20 mg renal reduction, the 280 mg/3.5 mL solution, and the reaction rates against placeboretrieved 2026-08-13FDA label
- Alekseeva GV, Bottaev NA, Goroshkova VV. [Use of semax at a follow-up of patients with posthypoxic encephalopathy]. Anesteziol Reanimatol. 1999;(1):40-3 — a follow-up of 73 patients recovering from oxygen starvation of the brain, fourteen of them in a persistent vegetative state. Reports paroxysmal activity on the electroencephalogram in some cases, and advises monitoring during the first injection. Russian; read through the indexed English abstractretrieved 2026-08-13limited human data
- Dorr RT, Lines R, Levine N, Brooks C, Xiang L. Evaluation of melanotan-II, a superpotent cyclic melanotropic peptide in a pilot phase-I clinical study. Life Sci. 1996;58(20):1777-84retrieved 2026-08-13limited human data
- Mallory CW, Lopategui DM, Cordon BH. Melanotan Tanning Injection: A Rare Cause of Priapism. Sex Med. 2021;9(1):100298retrieved 2026-08-13limited human data
- Nelson ME, Bryant SM, Aks SE. Melanotan II injection resulting in systemic toxicity and rhabdomyolysis. Clin Toxicol (Phila). 2012;50(10):1169-73retrieved 2026-08-13limited human data
- Peters B, Hadimeri H, Wahlberg R, Afghahi H. Melanotan II: a possible cause of renal infarction: review of the literature and case report. CEN Case Rep. 2020;9(3):219-222retrieved 2026-08-13limited human data
- Burian EA, Jemec GBE. Eruptive Melanocytic Nevi: A Review. Am J Clin Dermatol. 2019;20(5):669-682retrieved 2026-08-13limited human data
- Habbema L, Halk AB, Neumann M, Bergman W. Risks of unregulated use of alpha-melanocyte-stimulating hormone analogues: a review. Int J Dermatol. 2017;56(6):575-580retrieved 2026-08-13limited human data
- Gao L et al. Treatment With 9-mg Mazdutide for Weight Reduction in Chinese Adults With Obesity: The GLORY-2 Randomized Clinical Trial. JAMA 2026;336(5):377-388 — 60 weeks, ClinicalTrials.gov NCT06164873 (PMID 42251595)retrieved 2026-08-17Human trial
- Kamrul-Hasan ABM et al. Efficacy and Safety of the Dual GLP-1 and Glucagon Receptor Agonist Mazdutide in Predominantly Chinese Adults With Obesity and/or Type 2 Diabetes: A Systematic Review and Meta-Analysis. Diabetes Obes Metab 2026 — nine randomized trials, 2,292 participants, no manufacturer authorship (PMID 42410325)retrieved 2026-08-17Human trial
- Ji L et al. Once-Weekly Mazdutide in Chinese Adults with Obesity or Overweight. N Engl J Med 2025;392:2215-2225 (GLORY-1, NCT05607680, PMID 40421736)retrieved 2026-08-17Human trial
- Meshchaninov VN et al. [Effect of synthetic peptides on aging of patients with chronic polymorbidity and organic brain syndrome of the central nervous system in remission]. Adv Gerontol 2015;28(1):62-7 — 32 patients aged 41 to 83; reports prooxidant activity on chemiluminescence and a fall in CD34+ haematopoietic markers (PMID 26390612, in Russian)retrieved 2026-08-13limited human data
- Bays HE et al. Weekly Subcutaneous VK2735 for Weight Management: Phase 2 VENTURE Study. Obesity 2026;34:537-549 (NCT06068946, PMID 41508550)retrieved 2026-08-16Human trial
- Knop FK et al. Oral amycretin in adults with overweight or obesity: phase 1 trial (NCT05369390, PMID 40550229)retrieved 2026-08-17Human trial
- Jastreboff AM et al. Subcutaneous amycretin in adults with overweight or obesity: phase 1b/2a trial (NCT06064006, PMID 40550231)retrieved 2026-08-17Human trial
- Noureddin M et al. Pemvidutide in MASH: 24-week IMPACT phase 2b results (NCT05989711, PMID 41237796)retrieved 2026-08-17Human trial
- Altimmune SEC exhibit — RECLAIM phase 2 topline results in alcohol use disorderretrieved 2026-08-17Phase 2 results in a company SEC filing