Page last checked
Symptom question · incretin class
Does a GLP-1 cause diarrhea?
Yes. 6 of the 36 compounds here list diarrhea as a reported side effect. The rate differs by drug and study. The table below gives each source’s figure.
Source: checked against 36 compound guides; rates are shown exactly as reportedFDA label
The label gives a frequency measured in a trial. FDA data shows the share of later reports that mentioned diarrhea. The two sources use different methods, but here they point in the same direction.
Neither of them tells you whether it will happen to you, and neither is a probability for any one person. What they establish is that this is an expected, documented reaction rather than a surprise. That is a smaller claim than the one most pages on this question make.
Information checked 2026-08-20
At a glance
Compounds that list it
7 of 36
Only in a combined category
1
No published human safety data
11
Best available source
FDA label
Which compounds list diarrhea
We checked every covered compound for this one reaction. Three sources name it directly, and one includes it in a combined stomach-and-gut figure. The others either do not list it or have no human safety data. We keep those answers separate so a missing result is never mistaken for proof that a reaction cannot happen.
| Compound | How it appears | Frequency reported | Source type |
|---|---|---|---|
| TirzepatideZepbound, Mounjaro | Diarrhea | Very common (≥10%) | FDA label |
| SemaglutideWegovy, Ozempic, Rybelsus | Diarrhea | Very common (≥10%) | FDA label |
| LiraglutideVictoza, Saxenda | Diarrhea | Reported in Victoza trials (≥5%) | FDA label |
| Retatrutide | Diarrhea | Reported in trials (dose-dependent) | Human trial |
| Cagrilintide | Stomach and gut events overall (nausea, constipation, diarrhea)counted inside a grouped figure, not on its own | Reported in 41–63% across trial doses (vs 32% placebo) | 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 | Diarrhea | Reported by 39.4% on 9 mg weekly (vs 6.5% on placebo) | 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 | Diarrhea | In RECLAIM, the sponsor reported 20% with pemvidutide versus 10% with placebo | 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 | 9.0% of Ozempic reports | 66,161 reports |
| Rybelsussemaglutide | 7.9% of Rybelsus reports | 7,379 reports |
| Victozaliraglutide | 7.1% of Victoza reports | 44,086 reports |
| Trulicitydulaglutide | 6.9% of Trulicity reports | 88,332 reports |
| Mounjarotirzepatide | 6.3% of Mounjaro reports | 93,975 reports |
| Zepboundtirzepatide | 6.2% of Zepbound reports | 70,141 reports |
| Saxendaliraglutide | 5.5% of Saxenda reports | 10,040 reports |
| Wegovysemaglutide | 5.5% of Wegovy reports | 21,044 reports |
3Read deeper
Why the gut is where this class shows up
These compounds act on receptors that are not confined to the pancreas. The same signaling that slows how fast the stomach empties also acts along the intestine. The gut is dense with the nerves and muscle that signaling reaches. So a change in bowel habit is close to the drug’s known action rather than off to one side of it.
That is also why the same class produces both constipation and diarrhea, which sounds contradictory and is not. Motility can move in either direction, and which way it moves differs between people and between doses. Both reactions appear on the same labels, at the same frequency band, from the same trials.
This paragraph is general pharmacology rather than a value read off a record. It is here because the alternative invites the reader to supply their own account. The ones in circulation are worse.
The opposite reaction is on the same records
What neither document says about how long it lasts
A label frequency band answers how many people in a trial reported something. It does not answer when it started, how long it went on, or whether it settled. A share of FDA side-effect reports does not answer those either — a report records that something was filed, with no follow-up attached.
Neither source reports how long it lasted. That means there is no reliable duration to quote from them. A precise timeline from elsewhere would be based on a different source or on an estimate.
What this page does and does not establish
Diarrhea is the reaction where the evidence is strongest in this section, which makes it the easiest place to overclaim. Each row separates what the two documents support from what gets built on top of them.
| The claim | What the evidence shows |
|---|---|
| Diarrhea is a documented reaction of this class. | Established. Three sources name it and one includes it in a combined figure. FDA reports include it for all eight brands. |
| Roughly one in ten people taking it get diarrhea. | Not what the label says. A frequency band is the rate observed in a specific trial population on a specific schedule. Reading it as a personal probability drops the population, the dose and the comparison group. |
| Ozempic causes more diarrhea than Wegovy. | Not established by FDA reports. A larger share of reports does not mean a higher rate among everyone who used the product. The data does not include people who filed nothing, and report shares also change with market age and prescribing patterns. |
| It means the dose is too high. | Not established here, and not a judgment this page makes. Nothing in either document ties a reaction to a dose decision, and a dose decision belongs to the prescribing clinician. |
When this stops being a nuisance
Most of what is described above is uncomfortable rather than dangerous. Two things on these sources turn it into something to raise promptly, and both are on the labels.
Acute pancreatitis
UrgentAcute kidney injury from dehydration
PromptCommon questions
Is diarrhea listed on the Ozempic and Wegovy labels?
The semaglutide label used for both brand names lists it in its highest frequency range.
That record is a transcribed extract of the reactions its cited label reports most prominently, not a complete copy of the document. The full label, read by a pharmacist or clinician alongside the rest of a medicine list, is where a complete list belongs.
How long does it last?
No label or trial reports a set duration.
That is a real limit rather than an evasion. A frequency band counts people, not days, and an FDA side-effect report has no follow-up attached to it. A page giving you an exact week count is quoting something other than these two documents.
Why does the same drug cause both diarrhea and constipation?
Both are on the same labels, at the same frequency band, from the same trials.
Motility can shift in either direction, and these sources do not say what decides which. What they do establish is that neither reaction is the characteristic one, and a page reporting only whichever fits its argument is choosing.
Does it mean the medicine is working?
Nothing in these sources connects a reaction to whether the treatment is achieving anything.
No study shows that a side effect means the drug is working. Treating discomfort as a progress signal can encourage people to ignore symptoms they should report.
Why does the report-stream table have no dashed rows?
Because every one of the eight brands carries this term among its twenty-five most-reported, so every row is a measurement rather than a ceiling.
Most terms in this section are not like that. Where a term is missing from a product’s stored list, the honest statement is a bound. It sits at or below the twenty-fifth term’s count. That is what a dashed row means. This table has none, which is itself worth noticing.
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.
Every tirzepatide reaction, not only diarrhea
The full semaglutide profile behind its diarrhea entry
Which pages list constipation, beyond the diarrhea question
The nausea question, alongside diarrhea
The pages each diarrhea row is read from
How long diarrhea lasts, and why nobody says
What else mazdutide lists besides diarrhea
The full pemvidutide profile behind its diarrhea entry
Every cagrilintide reaction, not only diarrhea
- Zepbound (tirzepatide) — FDA-approved Prescribing Informationretrieved 2026-07-22FDA label
- Wegovy (semaglutide) — FDA-approved Prescribing Information (DailyMed)retrieved 2026-08-20FDA 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
- 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
- Altimmune SEC exhibit — RECLAIM phase 2 topline results in alcohol use disorderretrieved 2026-08-17Phase 2 results in a company SEC filing