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Symptom question · incretin class
Does Mounjaro cause fatigue?
Yes. 4 of the 36 compounds here list fatigue 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
Being listed means fatigue was reported during the trials behind the label. It does not prove what caused one person’s tiredness, how long it will last, or how much may come from other changes happening at the same time.
Information checked 2026-08-20
At a glance
Compounds that list it
5 of 36
Only in a combined category
1
No published human safety data
11
Best available source
FDA label
Which compounds list fatigue
Fatigue appears in the FDA labels for two compounds. Most early trial reports do not mention it. That difference may reflect how the documents report side effects, so it should not be used to rank the compounds.
| Compound | How it appears | Frequency reported | Source type |
|---|---|---|---|
| TirzepatideZepbound, Mounjaro | Fatigue | Common (1–10%) | FDA label |
| SemaglutideWegovy, Ozempic, Rybelsus | Fatigue | Common (1–10%) | 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 | Fatigue | 3.2% vs 0.5% on placebo | 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 | Fatigue | Reported in human safety work that reaches this page only through a review — no rate is published | 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 | Drowsiness and tirednesscounted inside a grouped figure, not on its own | Graded moderate in one of the two subjects who reached 0.03 mg/kg — the finding that set the trial’s recommended dose one step lower | 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 |
|---|---|---|
| Saxendaliraglutide | 4.3% of Saxenda reports | 10,040 reports |
| Wegovysemaglutide | 4.2% of Wegovy reports | 21,044 reports |
| Ozempicsemaglutide | 4.2% of Ozempic reports | 66,161 reports |
| Rybelsussemaglutide | 4.0% of Rybelsus reports | 7,379 reports |
| Zepboundtirzepatide | 3.5% of Zepbound reports | 70,141 reports |
| Victozaliraglutide | 3.2% of Victoza reports | 44,086 reports |
| Trulicitydulaglutide | 2.8% of Trulicity reports | 88,332 reports |
| Mounjarotirzepatide | 2.7% of Mounjaro reports | 93,975 reports |
3Read deeper
Why tiredness is plausible on this class, and why plausible is not proven
Several routes to tiredness sit on these sources already, without needing a new mechanism. Energy intake falls, sometimes sharply — decreased appetite is a listed reaction. Stomach and gut reactions cost fluid. And for anyone taking one of these compounds alongside insulin or a sulfonylurea, low blood sugar is a labeled risk. It shows up as weakness, shakiness and trouble concentrating rather than announcing itself as a blood sugar problem.
None of that is an attribution. Someone starting one of these compounds is usually changing several things at once: what they eat, how much, when, and often how they sleep. A reaction table cannot separate the compound from everything else going on around it. What the labeled records establish is that fatigue was recorded and reported at the band the table prints. Everything past that is a clinical question about one person.
Fatigue is also the reaction most likely to have another explanation entirely, several of which are worth finding. That is the practical argument for raising it rather than absorbing it.
The labeled cause of weakness that is not fatigue
What the split between labeled and investigational records tells you
A prescribing document is assembled from trials that recorded every event occurring to every participant, related or not, and reported them against a control group. That machinery is why a reaction as unspecific as fatigue reaches a label at all: it survives the comparison with placebo.
A phase 2 paper may only highlight the side effects that differed most between groups. For these drugs, that usually means stomach and gut problems. If fatigue is missing from an early trial report, that does not prove the drug causes less fatigue.
The practical consequence is narrow. Only the labeled rows in the table above support a comparison, and even they only support one between the two drugs that carry a band.
What the evidence shows—and what remains unknown
Fatigue is the reaction where the gap between what a table shows and what a reader wants from it is widest.
| The claim | What the evidence shows |
|---|---|
| Fatigue is a recognized reaction on these compounds. | Supported for the two FDA-labeled records, at the band each label states. It is not supported as a class-wide statement, because the investigational records here do not carry it. |
| My tiredness is caused by the medicine. | Not supported by any table. Pinning down a cause in one case is a clinical judgment. It weighs the medicine list, the timing, the diet and everything else that changed. A published frequency band sees none of that. |
| The investigational compounds are less tiring. | Not supported. Their trial reports emphasize the reactions that separated the arms. Silence in a paper is not a measurement of absence, and treating it as one compares documents rather than compounds. |
| It wears off as the body adjusts. | Not supported. Some sources say stomach and gut side effects ease while a dose is held, but they do not say the same about fatigue. |
| Feeling drained is just part of losing weight. | Unestablished, and a costly assumption. Several listed causes of weakness on these same records can be found and named. One of them is tied to a specific medicine combination. That is exactly the sort of thing that gets missed when a symptom is filed under expected. |
When tiredness is a reason to make contact
Fatigue on its own is rarely urgent. This section exists for a reason. Two of the serious reactions listed on these sources show up as weakness, dizziness or trouble concentrating, and nothing more specific. Both are worth catching early.
Acute kidney injury from dehydration
PromptHypoglycemia when combined with insulin or a sulfonylurea
PromptCommon questions
Is fatigue listed on the Mounjaro label?
The tirzepatide label lists fatigue as a common side effect. The table above shows the reported frequency.
Mounjaro and Zepbound contain the same drug but have different approved uses and separate prescribing labels. Check the label for the specific product you use.
How long does Mounjaro fatigue last?
No label or trial reports a set duration for fatigue.
It is worth noticing what the sources do and do not commit to. They describe stomach and gut side effects as easing while a dose is held; they say nothing equivalent about fatigue. Pages that answer this with some number of weeks are extending a statement about one reaction onto another.
Does semaglutide cause fatigue as well?
Yes. The semaglutide and tirzepatide labels both list fatigue in the same frequency range.
The two labels agree, but they are not a head-to-head trial. Their frequency ranges cannot rank one drug as better than the other.
Is fatigue worse when the dose goes up?
The labeled records band this reaction without splitting it by dose, so they do not answer that question.
What the sources do describe is that reactions cluster around the start of treatment and around each increase. The approved schedules hold each step for a stated minimum before the next one is considered. That is a pattern, not a prediction, and pacing is a decision for the prescribing clinician.
Could the tiredness be low blood sugar rather than the compound?
It could. The pages here name the circumstance in which that is a labeled risk: taking one of these compounds alongside insulin or a sulfonylurea.
Low blood sugar presents as shakiness, sweating, sudden hunger, a racing heartbeat or difficulty concentrating, which overlaps almost entirely with what people describe as fatigue. The medicine list is what distinguishes them, and the prescriber holds it.
Should I stop taking it if I am exhausted?
Your prescribing clinician should decide whether to hold, change or stop a dose.
Bring specifics to that conversation: when it started relative to a dose change, what you are eating now, what else is on the medicine list, and whether anything else changed at the same time. A precise account is worth more at an appointment than a vague one. It is also the part only the person taking the compound can supply.
Is fatigue the same as the tiredness people report after eating less?
The studies do not separate those possible causes.
Energy intake falls on these compounds by design — decreased appetite is a listed reaction on several records here. Whether one person’s tiredness runs through that route, through the compound directly, or through something unrelated is a clinical question. The honest position is that a reaction table cannot settle 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 fatigue
What else semaglutide lists besides fatigue
Constipation read the same way as fatigue
Nausea across every page, as with fatigue
All source-checked pages, not only those listing fatigue
Every AOD-9604 reaction, not only fatigue
Every Melanotan II reaction, not only fatigue
Reading fatigue for a length nobody published
PT-141 reactions in full, including fatigue
Questions readers ask
How can I combat fatigue on Mounjaro?
What are four warning signs of fatigue?
How to get rid of fatigue on GLP-1?
- 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
- 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