Semaglutide Side Effects: What Studies and Users Report
What FDA labels and clinical studies report for Semaglutide, how strong that evidence is, and what is still unknown.
Side effects reported in studies
Adverse reactions from the FDA label come first, then side effects reported in individual studies. Frequencies are quoted as the source gives them; animal results are labelled.
| Side effect | How common | Study type | Source |
|---|---|---|---|
| Most common adverse reactions (5% or more) | 5% or more of patients | FDA label | FDA label (Ozempic) |
| Nausea (placebo, 0.5 mg, 1 mg) | placebo 6.1%; 0.5 mg 15.8%; 1 mg 20.3% | FDA label | FDA label (Ozempic) |
| Discontinuation due to gastrointestinal adverse reactions | 3.1% (0.5 mg), 3.8% (1 mg) vs 0.4% placebo | FDA label | FDA label (Ozempic) |
| Nausea (placebo, 2.4 mg) | placebo 16%; 2.4 mg 44% | FDA label | FDA label (Wegovy) |
| Diarrhea (placebo, 2.4 mg) | placebo 16%; 2.4 mg 30% | FDA label | FDA label (Wegovy) |
| Vomiting (placebo, 2.4 mg) | placebo 6%; 2.4 mg 24% | FDA label | FDA label (Wegovy) |
| Discontinuation due to adverse reactions | 6.8% vs 3.2% placebo | FDA label | FDA label (Wegovy) |
| Nausea (placebo, 7 mg, 14 mg) | placebo 6%; 7 mg 11%; 14 mg 20% | FDA label | FDA label (Rybelsus, Ozempic tablets) |
| Abdominal pain (placebo, 7 mg, 14 mg) | placebo 4%; 7 mg 10%; 14 mg 11% | FDA label | FDA label (Rybelsus, Ozempic tablets) |
| Discontinuation due to gastrointestinal adverse reactions | 8% (14 mg), 4% (7 mg) vs 1% placebo | FDA label | FDA label (Rybelsus, Ozempic tablets) |
| Treatment-emergent adverse events | 91·2% vs 84·8% placebo | Human RCTn = 3808 | Lancet 2026, PMID 41865758 |
| Gastrointestinal events“Gastrointestinal adverse events were more common in the semaglutide group.” | Frequency not stated | Human RCTn = 1197 | The New England journal of medicine 2025, PMID 40305708 |
| Gastrointestinal events | 74.0% vs 42.2% placebo | Human RCTn = 307 | The New England journal of medicine 2025, PMID 40934115 |
| Gastrointestinal events and dysaesthesia | 70·8% (7·2 mg), 61·2% (2·4 mg), 42·8% (placebo) | Human RCTn = 1407 | The lancet. Diabetes & endocrinology 2025, PMID 40961952 |
| Gastrointestinal events | 30 vs 15 participants | Human RCTn = 101 | Nature medicine 2025, PMID 39455729 |
| Serious adverse events | 49.6% vs 53.8% placebo | Human RCTn = 3533 | The New England journal of medicine 2024, PMID 38785209 |
| Discontinuation due to adverse events | 6.7% vs 3.0% placebo | Human RCTn = 407 | The New England journal of medicine 2024, PMID 39476339 |
| Discontinuation due to adverse events | 16.6% vs 8.2% placebo | Human RCTn = 17604 | The New England journal of medicine 2023, PMID 37952131 |
| Serious adverse events | 13.3% vs 26.7% placebo | Human RCTn = 529 | The New England journal of medicine 2023, PMID 37622681 |
| Gastrointestinal events | 84.1% vs 82.7% liraglutide | Human controlled trialn = 338 | JAMA 2022, PMID 35015037 |
| Nausea and diarrhea | most common | Human RCTn = 1961 | The New England journal of medicine 2021, PMID 33567185 |
| Discontinuation for gastrointestinal events | 4.5% vs 0.8% placebo | Human RCTn = 1961 | The New England journal of medicine 2021, PMID 33567185 |
| Gastrointestinal events | 49.1% vs 26.1% placebo | Human RCTn = 803 | JAMA 2021, PMID 33755728 |
| Gastrointestinal events | 63·5% (2·4 mg), 57·5% (1·0 mg) vs 34·3% placebo | Human RCTn = 1210 | Lancet 2021, PMID 33667417 |
| Gastrointestinal events | 82.8% vs 63.2% placebo | Human RCTn = 611 | JAMA 2021, PMID 33625476 |
| Nausea, constipation, vomiting | nausea 42% vs 11%; constipation 22% vs 12%; vomiting 15% vs 2% (placebo) | Human RCTn = 320 | The New England journal of medicine 2021, PMID 33185364 |
| Gastrointestinal events“Gastrointestinal adverse events leading to discontinuation of oral semaglutide or placebo were more common with oral semaglutide.” | Frequency not stated | Human RCTn = 3183 | The New England journal of medicine 2019, PMID 31185157 |
| Gastrointestinal disorders | 43% and 44% (semaglutide 0·5, 1·0 mg) vs 33% and 48% (dulaglutide) | Human controlled trialn = 1201 | The lancet. Diabetes & endocrinology 2018, PMID 29397376 |
| Retinopathy complications | hazard ratio 1.76 (95% CI 1.11 to 2.78) | Human RCTn = 3297 | The New England journal of medicine 2016, PMID 27633186 |
| Gastrointestinal events | similar | Human observationaln = 18386 | JAMA internal medicine 2024, PMID 38976257 |
| Adverse effects | most evaluated adverse effects | Meta-analysis | International journal of obesity 2025, PMID 39396098 |
What is not known
- How common each effect is at the doses people use outside of studies.
- Effects that take longer to appear than the length of the published studies.
- How Semaglutide interacts with other medicines and supplements.
- Whether research-grade products, which are not checked by the FDA, behave like the material used in studies.
When to get medical help
This is not a complete list. A doctor or pharmacist can help you judge whether a symptom is related.
Common questions
What are the side effects of Semaglutide?
The FDA label lists most common adverse reactions (5% or more), nausea (placebo, 0.5 mg, 1 mg), discontinuation due to gastrointestinal adverse reactions among others. The table on this page gives how often each happened and links each source.
Is Semaglutide safe?
Semaglutide has an FDA-approved label that lists its known risks. That label covers the approved product used as prescribed, not compounded or research-chemical versions.
More on Semaglutide
Sources
- 1These highlights do not include all the information needed to use OZEMPIC ® safely and effectively. See full prescribing information for OZEMPIC. OZEMPIC (semaglutide) injection, for subcutaneous use FDA label (Ozempic), DailyMed · current labeldailymed.nlm.nih.govAccessed 2 Oct 2026
- 2These highlights do not include all the information needed to use WEGOVY ® safely and effectively. See full prescribing information for WEGOVY. WEGOVY (semaglutide) injection, for subcutaneous use WEGFDA label (Wegovy), DailyMed · current labeldailymed.nlm.nih.govAccessed 2 Oct 2026
- 3These highlights do not include all the information needed to use RYBELSUS ® and OZEMPIC ® tablets safely and effectively. See full prescribing information for RYBELSUS and OZEMPIC tablets. RYBELSUS (FDA label (Rybelsus, Ozempic tablets), DailyMed · current labeldailymed.nlm.nih.govAccessed 2 Oct 2026
- 4Efficacy and safety of oral semaglutide 14 mg (flexible dose) in early-stage symptomatic Alzheimer's disease (evoke and evoke+): two phase 3, randomised, placebo-controlled trials.Lancet (London, England) · 2026PMID 41865758Accessed 2 Oct 2026
- 5Phase 3 Trial of Semaglutide in Metabolic Dysfunction-Associated Steatohepatitis.The New England journal of medicine · 2025PMID 40305708Accessed 2 Oct 2026
- 6Oral Semaglutide at a Dose of 25 mg in Adults with Overweight or Obesity.The New England journal of medicine · 2025PMID 40934115Accessed 2 Oct 2026
- 7Once-weekly semaglutide 7·2 mg in adults with obesity (STEP UP): a randomised, controlled, phase 3b trial.The lancet. Diabetes & endocrinology · 2025PMID 40961952Accessed 2 Oct 2026
- 8Semaglutide in patients with overweight or obesity and chronic kidney disease without diabetes: a randomized double-blind placebo-controlled clinical trial.Nature medicine · 2025PMID 39455729Accessed 2 Oct 2026
- 9Effects of Semaglutide on Chronic Kidney Disease in Patients with Type 2 Diabetes.The New England journal of medicine · 2024PMID 38785209Accessed 2 Oct 2026
- 10Once-Weekly Semaglutide in Persons with Obesity and Knee Osteoarthritis.The New England journal of medicine · 2024PMID 39476339Accessed 2 Oct 2026
- 11Semaglutide and Cardiovascular Outcomes in Obesity without Diabetes.The New England journal of medicine · 2023PMID 37952131Accessed 2 Oct 2026
- 12Semaglutide in Patients with Heart Failure with Preserved Ejection Fraction and Obesity.The New England journal of medicine · 2023PMID 37622681Accessed 2 Oct 2026
- 13Effect of Weekly Subcutaneous Semaglutide vs Daily Liraglutide on Body Weight in Adults With Overweight or Obesity Without Diabetes: The STEP 8 Randomized Clinical Trial.JAMA · 2022PMID 35015037Accessed 2 Oct 2026
- 14Once-Weekly Semaglutide in Adults with Overweight or Obesity.The New England journal of medicine · 2021PMID 33567185Accessed 2 Oct 2026
- 15Effect of Continued Weekly Subcutaneous Semaglutide vs Placebo on Weight Loss Maintenance in Adults With Overweight or Obesity: The STEP 4 Randomized Clinical Trial.JAMA · 2021PMID 33755728Accessed 2 Oct 2026
- 16Semaglutide 2·4 mg once a week in adults with overweight or obesity, and type 2 diabetes (STEP 2): a randomised, double-blind, double-dummy, placebo-controlled, phase 3 trial.Lancet (London, England) · 2021PMID 33667417Accessed 2 Oct 2026
- 17Effect of Subcutaneous Semaglutide vs Placebo as an Adjunct to Intensive Behavioral Therapy on Body Weight in Adults With Overweight or Obesity: The STEP 3 Randomized Clinical Trial.JAMA · 2021PMID 33625476Accessed 2 Oct 2026
- 18A Placebo-Controlled Trial of Subcutaneous Semaglutide in Nonalcoholic Steatohepatitis.The New England journal of medicine · 2021PMID 33185364Accessed 2 Oct 2026
- 19Oral Semaglutide and Cardiovascular Outcomes in Patients with Type 2 Diabetes.The New England journal of medicine · 2019PMID 31185157Accessed 2 Oct 2026
- 20Semaglutide versus dulaglutide once weekly in patients with type 2 diabetes (SUSTAIN 7): a randomised, open-label, phase 3b trial.The lancet. Diabetes & endocrinology · 2018PMID 29397376Accessed 2 Oct 2026
- 21Semaglutide and Cardiovascular Outcomes in Patients with Type 2 Diabetes.The New England journal of medicine · 2016PMID 27633186Accessed 2 Oct 2026
- 22Semaglutide vs Tirzepatide for Weight Loss in Adults With Overweight or Obesity.JAMA internal medicine · 2024PMID 38976257Accessed 2 Oct 2026
- 23Semaglutide effects on safety and cardiovascular outcomes in patients with overweight or obesity: a systematic review and meta-analysis.International journal of obesity (2005) · 2025PMID 39396098Accessed 2 Oct 2026
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