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Symptom question · incretin class
Does GLP-1 medication cause hair loss?
None of the 36 compound guides checked lists hair loss 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
That describes these sources, not the compounds themselves. A gap can mean nobody saw the effect, nobody tied it to treatment, or the source reported it elsewhere. Those are different situations. A reaction table cannot tell them apart.
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 hair loss
None of the labels or studies checked lists hair loss as a reported side effect. The table keeps that result blank instead of turning stories or assumptions into a percentage.
| 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 |
| Zepboundtirzepatide | 2.3% of Zepbound reports | 70,141 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 |
| Saxendaliraglutide | below 1.9% of Saxenda reports | 10,040 reports |
| Mounjarotirzepatide | below 1.7% of Mounjaro reports | 93,975 reports |
| Victozaliraglutide | below 1.7% of Victoza reports | 44,086 reports |
3Read deeper
Why the question arises at all
Hair grows on a cycle. Each follicle spends a long stretch growing and a short stretch at rest before the hair sheds. Shedding that shows up weeks or months after a physical stress is a recognized pattern in general medicine. The stress can be a big, fast change in body weight, an illness, surgery, or a sharp change in what someone eats. The pattern is about the stress, not about any particular cause of it.
That is why people ask about hair loss after fast weight loss, however the weight came off. But none of the studies in this comparison measured whether that explains one person’s shedding.
This is general physiology, not a measured result for these compounds. It explains why the question is reasonable without inventing a rate.
What it would take to answer this properly
A publishable answer would need a defined group, an untreated comparison group, a set way to measure shedding, and enough follow-up time. Those features separate a reaction rate from an impression. They also explain why a weight-loss trial cannot be read as a hair-loss study.
Reports gathered outside such a structure are real experiences and they are not nothing — but they cannot be counted. There is no denominator. People who did not experience it never post, so what you can see is skewed from the start. No amount of it adds up to a rate.
No cited study has published a measurement. If that changes, the result should be shown with its sample size, comparison group and citation rather than replaced with an estimate.
Four readings of the same absence
An empty cell invites interpretation, and most of the interpretations in circulation run in whichever direction the writer already favored. Each row below is a claim that gets made in both directions from the same non-result.
| The claim | What the evidence shows |
|---|---|
| These compounds do not cause hair loss. | Not supported. Nothing here looked for it and reported a null result. A gap in a reaction table is not a measured finding of no effect. Citing it as one is the same mistake as citing it the other way. |
| These compounds cause hair loss. | Not supported by these labels or trials. None lists hair loss or gives a rate for it. |
| The label would say so if it happened. | Overstated. A label lists what trials recorded and what later monitoring pinned on the drug. Effects that arrive late, or that get put down to weight change rather than to the drug, are the hardest kind to capture that way. |
| It is caused by the weight loss, not the medicine. | Plausible and unestablished. It is the general pattern the section above describes. Separating a consequence of fast weight change from an effect of the drug causing it needs a study design nobody cited here used. |
Taking this to a clinician
Shedding has a long list of causes that have nothing to do with these compounds. Thyroid problems and iron levels are among the ones usually checked first. Several of them can be found and treated.
Common questions
Is hair loss listed as a side effect of Ozempic or Wegovy?
Not in the semaglutide side-effect summary used for both brand names.
That summary is an extract, not the full prescribing label. A pharmacist or clinician can check the complete label for a specific product.
Is it the medication or the weight loss?
The cited sources cannot separate the two causes.
Hair shedding can follow rapid weight change. Separating that from a direct drug effect would require a trial designed for the question, and none of these trials was.
How long does it last, and does hair grow back?
No label or trial in this comparison reports a duration or recovery rate.
That is a real limit rather than an evasion. What happens next depends on the cause, and finding the cause is a clinical assessment rather than a search result. That is why this question routes to a clinician.
Do the different GLP-1 compounds differ on this?
The available labels and trials do not support a ranking because none reports hair loss as a measured side effect.
A comparison needs two measurements. With none, any claim that one compound is gentler on hair than another has no source underneath it. Confidence in the phrasing does not change that.
Would supplements or a higher protein intake prevent it?
No cited trial evaluates a treatment or supplement for this purpose, so none is recommended.
Several labels list decreased appetite as a side effect. Eating less can make it harder to get enough protein and other nutrients, but the right plan depends on the person. A clinician or dietitian can help set one.
Why do so many pages give a percentage for this?
Because a number performs better than an absence, and nothing stops a page from printing one.
Figures in this area are usually lifted from a study of different people, a different treatment or a different question. They then get repeated without the qualifier that made them mean anything. This site’s build gate blocks any clinical value with no citation attached. That is why this page has an empty table rather than a plausible one.
Is muscle loss a different question from this one?
Yes, and the reason the two absences are different is worth stating.
A side-effect table is designed to capture hair loss, and these sources do not list it. Lean mass is not a side effect. It is a body-composition measurement, taken with different instruments for a different purpose. It would not appear in that table even if someone had measured it. That distinction is set out on the muscle-loss page in this section.
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 hair loss
The full semaglutide profile behind its hair loss entry
The constipation question, alongside hair loss
The nausea question, alongside hair loss
The pages each hair loss row is read from
How long hair loss lasts, and why nobody says
From a hair loss page to an exact syringe draw
All the cross-compound reads, including hair loss
Tirzepatide beyond its hair loss listing
- 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