Semaglutide side effects and risks
A GLP-1 medicine with strong weight, glucose, heart and kidney evidence; dose and formulation matter.
Also called: Ozempic, Wegovy, Wegovy HD, Wegovy FlexTouch, Rybelsus, oral semaglutide, NN9535, NN9924.
GLP-1 / GIP / glucagon agonists · GLP-1 receptor agonist · Evidence: Approved drug.
Reported side effects
- US boxed warning: thyroid C-cell tumors: Semaglutide caused thyroid C cell tumors in rodents. Whether it causes these tumors in humans is unknown., serious. Avoid with personal or family MTC or MEN2. Report a neck lump, trouble swallowing or persistent hoarseness. (source)
- Nausea: 2.4 mg injection: 44% versus 16% placebo., moderate. Smaller meals and fluids may help; persistent or severe symptoms need review. (source)
- Diarrhea: 2.4 mg injection: 30% versus 16% placebo., moderate. Smaller meals and fluids may help; persistent or severe symptoms need review. (source)
- Vomiting: 2.4 mg injection: 24% versus 6% placebo., moderate. Smaller meals and fluids may help; persistent or severe symptoms need review. (source)
- Constipation: 2.4 mg injection: 24% versus 11% placebo., moderate. Smaller meals and fluids may help; persistent or severe symptoms need review. (source)
- Abdominal pain: 2.4 mg injection: 20% versus 10% placebo., moderate. Smaller meals and fluids may help; persistent or severe symptoms need review. (source)
- Headache: 2.4 mg injection: 14% versus 10% placebo., moderate. Smaller meals and fluids may help; persistent or severe symptoms need review. (source)
- Fatigue: 2.4 mg injection: 11% versus 5% placebo., moderate. Smaller meals and fluids may help; persistent or severe symptoms need review. (source)
- Burping, reflux or indigestion: 2.4 mg: burping 7%, reflux 5%, indigestion 9%; placebo <1%, 3%, 3%., moderate (source)
- Hair loss: 2.4 mg: 3% versus 1% placebo; 7.2 mg: 6% versus 1% placebo., moderate (source)
- Altered or painful skin sensation: Pooled 7.2/2.4 mg/placebo: 22%/6%/0.3%., moderate. Report lasting burning, numbness or painful touch; a dose change may be needed. (source)
- Gallstones: 2.4 mg injection: 1.6% versus 0.7% placebo; oral Wegovy: 2.5% versus 1%., serious (source)
- Gallbladder inflammation: 2.4 mg injection: 0.6% versus 0.2% placebo., serious (source)
- Low blood sugar: Wegovy in diabetes, without insulin: 6.2% versus 2.5% placebo below 54 mg/dL., serious. Risk rises with insulin or sulfonylureas; those medicines may need adjustment. (source)
Stop and get help if
- Severe lasting upper abdominal pain, with or without vomiting: Stop semaglutide and get urgent assessment for pancreatitis.
- Face or throat swelling, breathing trouble or fainting: Stop the drug and call emergency services for possible severe allergy.
- Sudden vision loss or rapidly worsening sight: Get urgent eye care today; confirmed NAION requires stopping semaglutide.
- Confusion, seizure, unconsciousness or low sugar that will not resolve: Call emergency services; severe low blood sugar needs immediate care.
- Repeated vomiting, inability to drink, or very little urine: Get urgent care for dehydration, kidney injury or overdose.
- Severe bloating, vomiting, and no stool or gas: Get urgent care for possible bowel obstruction.
- Right upper abdominal pain with fever, jaundice or pale stool: Get urgent assessment for gallbladder or bile-duct disease.
- Chest pain, fainting or persistent racing heart at rest: Seek urgent care; call emergency services for chest pain or collapse.
Who should avoid it
- mtcOrMen2: US labels contraindicate use with personal or family medullary thyroid cancer or MEN2.
- pregnant: Stop weight-loss use when pregnancy is recognized; diabetes or MASH needs a separate clinician benefit-risk decision.
- tryingToConceive: Stop at least 2 months before planned pregnancy because the drug clears slowly.
- breastfeeding: Oral labels advise against breastfeeding; eight injection users cannot establish infant safety.
- under18: Wegovy injection is also approved for selected ages 12+; this is not a universal pediatric drug contraindication.
- eatingDisorderHistory: Assess nutrition and specialist support.
- other: Do not use after serious allergy to semaglutide or product ingredients.
- pancreatitisHistory: Past pancreatitis needs review. Stop and assess immediately if pancreatitis is suspected.
- gallbladderDisease: Gallstones and gallbladder inflammation can occur, including during rapid weight loss.
- gastroparesis: US labels do not recommend use with severe gastroparesis; review persistent vomiting or very slow stomach emptying.
- diabeticRetinopathy: Rapid glucose improvement can worsen existing diabetic eye disease; arrange eye monitoring.
- kidneyDisease: Dehydration can injure kidneys. US labels do not require routine renal dose adjustment; EU Wegovy restricts severe impairment.
- liverDisease: US labels do not require routine liver dose adjustment. Cirrhosis is outside the approved MASH population.
- heartCondition: Resting heart rate can rise; assess persistent racing, fainting or severe dizziness.
- diabetes: Review glucose medicines and eye history; semaglutide does not replace required insulin.
- surgeryPlanned: Slow stomach emptying can cause aspiration under anesthesia. Tell the team the formulation, dose and last dose date.
- other: Prior NAION needs eye-specialist review; new vision loss needs urgent care. Stop semaglutide if NAION is confirmed.
- depressionOrSuicidalThoughts: Seek help for new suicidal thoughts. FDA found no increased drug-related risk and requested warning removal January 13, 2026.
- testedAthlete: WADA monitors semaglutide markers in and out of competition in 2026; monitoring is not prohibition.
Interactions
- Insulin: Raises low-sugar risk. Insulin changes need glucose-guided adjustment; do not abruptly stop required insulin.
- Sulfonylureas and insulin releasers: These medicines release insulin and can cause low blood sugar with semaglutide.
- Other semaglutide or GLP-1 medicines: Avoid duplicate GLP-1 activity. Wegovy label does not recommend other semaglutide or GLP-1 medicines.
- Levothyroxine: Oral semaglutide increased thyroxine exposure by 33% in a PK study; review timing and thyroid tests.
- Warfarin and coumarins: No important warfarin PK change shown; EU guidance recommends frequent INR checks when starting semaglutide.
- Oral medicines needing close monitoring: Slower stomach emptying may alter absorption. Review drug levels where used; an interaction is not established for every listed drug.
- Oral contraceptives: Tested contraceptive exposure was not reduced. Vomiting or severe diarrhea still needs the pill’s missed-dose advice.
- Other morning tablets with oral semaglutide: Take oral semaglutide first; wait ≥30 minutes before other oral medicines. These tested drugs showed no major PK effect.
Product quality risks
- A 2024 test-purchase study received 3 of 6 online orders. Tested products had 7–14% purity and 29–39% more semaglutide than claimed.
- One sample had elevated endotoxin; no viable microbes were found. A small negative sterility sample does not establish safe production.
- FDA found counterfeit Ozempic in the legitimate US supply chain; authentic lot numbers alone do not prove authenticity.
- FDA reports compounded-vial mistakes of 5–20 times the intended dose. Milligrams, milliliters and syringe units differ.
- Semaglutide sodium and acetate differ from approved semaglutide; FDA does not know that they have the same properties.
Related to Semaglutide
- Tirzepatide: A weekly GIP/GLP-1 injection with strong diabetes and weight-loss evidence and common stomach side effects.
- Retatrutide: An experimental weekly injection with phase 3 weight-loss results.
- Liraglutide: A daily GLP-1 injection approved for weight management and type 2 diabetes.
- Dulaglutide: A weekly GLP-1 medicine approved for type 2 diabetes and lower heart-event risk.
- Exenatide: An older GLP-1 with twice-daily and weekly forms, now widely discontinued.
- Cagrilintide: An unapproved weekly amylin analogue with weight-loss trials and common stomach symptoms.
Sources
- Canada approves first generic semaglutide for weight loss, 2026
- FDA clarifies policies for compounders as national GLP-1 supply begins to stabilize, FDA · 2026
- FDA Proposes to Exclude Semaglutide, Tirzepatide, and Liraglutide on 503B Bulks List, FDA · 2026
- FDA Requests Removal of Suicidal Behavior and Ideation Warning from Glucagon-Like Peptide-1 Receptor Agonist (GLP-1 RA) Medications, FDA · 2026
- FDA Warns 30 Telehealth Companies Against Illegal Marketing of Compounded GLP-1s, 2026
- FDA’s Concerns with Unapproved GLP-1 Drugs Used for Weight Loss, FDA · FDA · 2026
- First GLP-1 tablet for weight loss approved in the UK, 2026
- Ozempic injection US prescribing information, July 2026; DailyMed Set ID 42bdd912-2393-44c4-b7e0-47672ca28991, 2026
- Rybelsus, INN-semaglutide, 2026
- Single-dose 7.2mg semaglutide (Wegovy) pen approved to treat adult patients with obesity, 2026
- The 2026 Monitoring Program, World Anti-Doping Agency · 2026
- These 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 (semaglutide) tablets, for oral use OZEMPIC (semaglutide) tablets, for oral use Initial U.S. Approval: 2017, 2026
- Wegovy semaglutide prescribing information: injection strengths, DailyMed · 2026
- WEGOVY- semaglutide injection, solution WEGOVY- semaglutide tablet, DailyMed · DailyMed · 2026
- Wegovy, INN-semaglutide, 2026
Sources checked: 2026-10-18.
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