LOSE WEIGHT WITH MEDICAL SUPPORT — BUILT FOR MEN
- Your personalised programme is built around medical care, not willpower.
- No generic diets. No guesswork.
- Just science-backed results and expert support.
Find out if you’re eligible

Rybelsus (semaglutide) is an oral GLP-1 receptor agonist licensed in the UK for type 2 diabetes mellitus. Does Rybelsus cause gas? Yes, gastrointestinal side effects including gas and bloating are recognised adverse reactions, though severity varies between individuals. These symptoms relate to semaglutide's mechanism of action—slowing gastric emptying and altering gut motility. According to the UK Summary of Product Characteristics, abdominal distension and dyspepsia (which encompass gas and bloating) are common adverse reactions. Most gastrointestinal symptoms occur during initial treatment weeks and often improve as the body adjusts, though individual experiences differ considerably.
Quick Answer: Rybelsus (semaglutide) commonly causes gas and bloating as recognised gastrointestinal adverse reactions, classified as common side effects affecting up to 1 in 10 patients.
Rybelsus (semaglutide) is an oral glucagon-like peptide-1 (GLP-1) receptor agonist licensed in the UK for the treatment of type 2 diabetes mellitus. Gastrointestinal side effects, including gas and bloating, are recognised adverse reactions associated with this medication, though the frequency and severity vary considerably between individuals.
The mechanism by which Rybelsus may contribute to gas and bloating relates to its pharmacological action. Semaglutide works by mimicking the naturally occurring hormone GLP-1, which slows gastric emptying—the rate at which food moves from the stomach into the small intestine. This delayed gastric emptying can lead to a sensation of fullness and abdominal distension. Additionally, GLP-1 receptor agonists affect gut motility throughout the gastrointestinal system, which may alter the normal transit of intestinal contents and contribute to symptoms of bloating and gas.
According to the UK Summary of Product Characteristics (SmPC) for Rybelsus, gastrointestinal disorders are very common adverse reactions, with nausea, diarrhoea, and vomiting specifically listed as very common (affecting ≥1/10 patients). Abdominal pain, constipation, dyspepsia, gastritis, and abdominal distension are classified as common adverse reactions (affecting ≥1/100 to <1/10 patients).
Patients starting Rybelsus should be aware that gastrointestinal symptoms typically occur during the initial weeks of treatment and often improve as the body adjusts to the medication, though the timeframe for improvement varies between individuals.

Gastrointestinal adverse effects are the most frequently reported side effects associated with Rybelsus therapy. According to the UK SmPC and European Public Assessment Report (EPAR), the following frequencies are observed:
Nausea: Very common (≥1/10 patients)
Diarrhoea: Very common (≥1/10 patients)
Vomiting: Very common (≥1/10 patients)
Abdominal pain: Common (≥1/100 to <1/10 patients)
Constipation: Common (≥1/100 to <1/10 patients)
Dyspepsia and abdominal distension: Common (≥1/100 to <1/10 patients)
Whilst gas (flatulence) is not always separately quantified in pivotal trials, it falls within the broader category of abdominal distension and dyspepsia, which are classified as common adverse reactions. Clinical experience suggests that bloating and flatulence may be particularly noticeable during dose escalation, though individual responses vary considerably.
The incidence of gastrointestinal side effects appears to be dose-dependent. Rybelsus is initiated at 3 mg once daily for 30 days, then increased to 7 mg daily, with a possible further increase to 14 mg daily if additional glycaemic control is required. Higher doses are associated with increased rates of gastrointestinal symptoms. Many patients report that symptoms tend to diminish over time, though the precise timeframe for improvement varies.
It is worth noting that gastrointestinal side effects are a class effect of GLP-1 receptor agonists, observed across all medications in this therapeutic category, including injectable formulations such as Ozempic and Victoza. When Rybelsus is used in combination with insulin or sulfonylureas, there is an increased risk of hypoglycaemia, which should be monitored.
For patients experiencing gas and bloating whilst taking Rybelsus, several evidence-based strategies may help minimise discomfort and improve tolerability:
Dietary modifications can play a significant role in reducing gastrointestinal symptoms:
Eat smaller, more frequent meals rather than large portions, as this reduces the burden on delayed gastric emptying
Avoid foods known to produce gas, including beans, lentils, cruciferous vegetables (broccoli, cauliflower, cabbage), carbonated beverages, and high-fat foods
Reduce intake of artificial sweeteners (sorbitol, mannitol) which can ferment in the gut
Chew food thoroughly and eat slowly to minimise air swallowing (aerophagia)
Stay well hydrated to support normal digestive function
Lifestyle adjustments may also prove beneficial:
Regular physical activity, such as walking after meals, can promote gut motility and help disperse trapped gas
Avoid lying down immediately after eating, as this can exacerbate bloating when gastric emptying is already delayed
Keep a food and symptom diary to identify specific triggers
Medication timing and adherence are crucial. According to the SmPC, Rybelsus must be taken on an empty stomach with no more than 120 mL of water, at least 30 minutes before the first food, drink, or other oral medications of the day. The tablet should be swallowed whole; do not split, crush or chew. If a dose is missed, the missed dose should be skipped, and the next dose taken the following day.
Over-the-counter remedies such as simeticone (an anti-foaming agent) may provide symptomatic relief for gas, though patients should consult their GP or pharmacist before adding any new medication. Evidence for probiotics in managing GLP-1-related gastrointestinal symptoms remains limited, and there is no official recommendation for their routine use.
Patients should not discontinue Rybelsus without medical advice, as abrupt cessation may lead to deterioration in glycaemic control.
Whilst mild gastrointestinal symptoms are common and often self-limiting, certain situations warrant prompt medical review. Patients should contact their GP or diabetes specialist nurse if:
Symptoms are severe or persistent despite management strategies
Bloating is accompanied by severe abdominal pain, particularly if localised or progressively worsening
There is persistent vomiting or diarrhoea that may lead to dehydration and subsequent risk of acute kidney injury
Signs of dehydration develop, including reduced urine output, dizziness, or excessive thirst
Persistent right upper abdominal pain, fever or jaundice occurs, which may indicate gallbladder problems (cholelithiasis or cholecystitis), which have been reported with GLP-1 receptor agonists
New or unexplained symptoms emerge, such as blood in stools or unintentional weight loss beyond expected therapeutic effect
Serious gastrointestinal complications, though rare, have been reported with GLP-1 receptor agonists. According to the SmPC, acute pancreatitis is an uncommon but serious adverse reaction that presents with severe, persistent abdominal pain often radiating to the back, and may be accompanied by nausea and vomiting. Patients experiencing such symptoms should seek urgent medical attention via NHS 111 or 999/A&E if symptoms are severe.
The SmPC advises that Rybelsus is not recommended in patients with severe gastrointestinal disease, including severe gastroparesis. Patients with significant gastrointestinal symptoms should be monitored closely, particularly for signs of dehydration which may worsen renal function.
If gastrointestinal side effects significantly impair quality of life despite management strategies, healthcare professionals may consider dose adjustment or switching to an alternative glucose-lowering therapy. Patients should never adjust their dose independently. A structured approach to side effect management, in partnership with the diabetes care team, optimises both treatment adherence and clinical outcomes.
Patients are encouraged to report any suspected adverse reactions to Rybelsus via the MHRA Yellow Card Scheme (yellowcard.mhra.gov.uk or the Yellow Card app).
Gastrointestinal symptoms including gas and bloating typically occur during the initial weeks of Rybelsus treatment and often improve as the body adjusts to the medication, though the timeframe for improvement varies considerably between individuals.
Over-the-counter remedies such as simeticone may provide symptomatic relief for gas, though patients should consult their GP or pharmacist before adding any new medication. Dietary modifications and lifestyle adjustments are first-line management strategies.
Patients should not discontinue Rybelsus without medical advice, as abrupt cessation may lead to deterioration in glycaemic control. Contact your GP if symptoms are severe or persistent, as dose adjustment or alternative therapy may be considered.
All medical content on this blog is created based on reputable, evidence-based sources and reviewed regularly for accuracy and relevance. While we strive to keep content up to date with the latest research and clinical guidelines, it is intended for general informational purposes only.
DisclaimerThis content is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare professional with any medical questions or concerns. Use of the information is at your own risk, and we are not responsible for any consequences resulting from its use.