Mounjaro®
Dual-agonist support that helps curb appetite, hunger, and cravings to drive substantial, sustained weight loss.
- ~22.5% average body weight loss
- Significant weight reduction
- Improves blood sugar levels
- Clinically proven weight loss

GLP-1 receptor agonists, such as semaglutide and liraglutide, are increasingly prescribed in the UK for type 2 diabetes and weight management. Many patients with irritable bowel syndrome (IBS) wonder whether these medications might help their digestive symptoms. However, GLP-1 medications are not licensed or recommended for treating IBS. Whilst they affect gut function by slowing gastric emptying and influencing motility, their gastrointestinal side effects—including nausea, diarrhoea, constipation, and bloating—may overlap with or potentially worsen existing IBS symptoms. Understanding how GLP-1 medications interact with IBS is essential for safe, effective management of both conditions.
Summary: GLP-1 receptor agonists are not licensed or recommended for treating IBS and may worsen symptoms due to gastrointestinal side effects.
Glucagon-like peptide-1 (GLP-1) receptor agonists are a class of medications originally developed for managing type 2 diabetes and, more recently, some have been approved for weight management. In the UK, commonly prescribed GLP-1 medications include semaglutide (Ozempic for diabetes, Wegovy for weight management), liraglutide (Victoza for diabetes, Saxenda for weight management), and dulaglutide (Trulicity for diabetes). It's important to note that GLP-1 medications are not licensed or recommended for treating irritable bowel syndrome (IBS).
These medicines work by mimicking a naturally occurring hormone produced in the intestine that plays several important roles in metabolic regulation. The primary mechanism of action involves stimulating insulin secretion from the pancreas in a glucose-dependent manner, meaning they only work when blood sugar levels are elevated. This reduces the risk of hypoglycaemia compared to some other diabetes medications. GLP-1 receptor agonists also suppress glucagon release, a hormone that raises blood glucose, and slow gastric emptying—the rate at which food leaves the stomach and enters the small intestine. This delayed gastric emptying contributes to increased satiety and reduced appetite, which explains their effectiveness in weight management.
Additionally, GLP-1 medications have effects throughout the gastrointestinal tract, as GLP-1 receptors are widely distributed in the gut. They influence gut motility, intestinal secretions, and may affect the gut-brain axis—the bidirectional communication system between the digestive system and the central nervous system. These medications should be used with caution in people with severe gastrointestinal disease, including severe gastroparesis. Whilst these medications have proven benefits for glycaemic control and weight loss, their effects on gastrointestinal function mean they can influence digestive symptoms, which is particularly relevant for individuals with pre-existing bowel conditions such as IBS.
Irritable bowel syndrome (IBS) is a common functional gastrointestinal disorder affecting approximately 10-20% of the UK population. According to NICE guidelines (CG61), IBS is diagnosed based on clinical criteria when patients experience abdominal pain or discomfort that has been present for at least 6 months, is associated with defecation or a change in bowel habit, and with at least two of the following: altered stool frequency, altered stool form, altered stool passage, mucus in stool, or bloating/distension.
IBS presents in several subtypes, often classified using the Bristol Stool Chart:
IBS with constipation (IBS-C): Predominant hard or lumpy stools
IBS with diarrhoea (IBS-D): Predominant loose or watery stools
IBS with mixed bowel habits (IBS-M): Alternating constipation and diarrhoea
IBS unclassified (IBS-U): Insufficient abnormality of stool consistency
Common symptoms include bloating, abdominal distension, urgency, and a sensation of incomplete evacuation. Many patients also report that symptoms worsen after eating, particularly following large meals or specific trigger foods. The exact cause of IBS remains incompletely understood, but contributing factors include visceral hypersensitivity (increased pain perception in the gut), altered gut motility, changes in the gut microbiome, low-grade inflammation, and psychological factors such as stress and anxiety.
Diagnosis involves a positive symptom-based approach after excluding 'red flag' indicators. Initial investigations typically include full blood count, inflammatory markers (CRP/ESR), and coeliac serology. Faecal calprotectin testing may be used to help distinguish IBS from inflammatory bowel disease when there is diagnostic uncertainty.
Dietary triggers vary considerably between individuals but commonly include fatty foods, caffeine, alcohol, artificial sweeteners, and fermentable carbohydrates (FODMAPs). Stress, hormonal changes, and certain medications can also exacerbate symptoms. The heterogeneous nature of IBS means that treatment must be individualised, focusing on the predominant symptom pattern and identified triggers. Understanding your specific IBS subtype and triggers is crucial when considering how any new medication, including GLP-1 receptor agonists, might affect your symptoms.
Gastrointestinal side effects are the most commonly reported adverse reactions with GLP-1 receptor agonists, occurring in a significant proportion of patients, particularly during treatment initiation and dose escalation. According to product information, the most frequent symptoms include nausea, vomiting, diarrhoea, constipation, abdominal pain, and bloating. The frequency varies by medication and dose. These effects are directly related to the medication's mechanism of slowing gastric emptying and affecting gut motility.
For individuals with pre-existing IBS, these gastrointestinal effects may overlap with or potentially worsen existing symptoms. There is currently no official link established between GLP-1 medications and the development or exacerbation of IBS specifically, as IBS is a functional disorder rather than a structural disease. However, the symptomatic overlap means that patients with IBS may find it challenging to distinguish between their baseline condition and medication-related side effects.
Patients with IBS-D (diarrhoea-predominant) may be particularly concerned about GLP-1-induced diarrhoea, whilst those with IBS-C (constipation-predominant) might experience either improvement or worsening depending on individual response. The delayed gastric emptying caused by GLP-1 medications can lead to feelings of fullness, bloating, and nausea—symptoms that many IBS patients already experience.
Important safety considerations include:
Pancreatitis risk: If you develop severe, persistent abdominal pain that may radiate to your back, with or without vomiting, stop taking the medication and seek urgent medical attention
Gallbladder disease: Sudden pain in the upper right abdomen, fever, or yellowing of the skin/eyes requires urgent medical review
GLP-1 medications are not recommended in people with severe gastrointestinal disease, including severe gastroparesis
Clinical considerations include:
Starting with the lowest available dose and titrating slowly
Monitoring symptom patterns carefully during initiation
Distinguishing between temporary side effects (which often lessen over weeks) and persistent symptom changes
Adjusting dietary intake, particularly meal size and composition
Most gastrointestinal side effects of GLP-1 medications are dose-dependent and tend to diminish over time as the body adapts. However, if you have IBS and are considering or currently taking a GLP-1 medication, close monitoring and communication with your healthcare team is essential to optimise both conditions effectively. Suspected side effects can be reported via the MHRA Yellow Card scheme (yellowcard.mhra.gov.uk).
NICE recommends a stepwise approach to IBS management, beginning with lifestyle modifications and progressing to pharmacological interventions based on symptom severity and predominant subtype. First-line management focuses on patient education, reassurance, and identifying individual triggers through dietary and lifestyle assessment.
Dietary interventions form a cornerstone of IBS management:
General dietary advice: Regular meal patterns, adequate hydration (8 glasses of fluid daily), limiting caffeine and alcohol, and reducing fatty or spicy foods
Fibre modification: Soluble fibre (such as ispaghula/psyllium) may help, whilst insoluble fibre (bran) can worsen symptoms
Low FODMAP diet: A structured elimination and reintroduction protocol, supervised by a registered dietitian, can identify specific carbohydrate triggers
Probiotics: Certain strains may provide benefit, though evidence varies
Pharmacological treatments are tailored to predominant symptoms:
For IBS-D: Loperamide (antimotility agent) for diarrhoea; low-dose tricyclic antidepressants (e.g., amitriptyline 10mg at night, with gradual titration) for pain and altered motility
For IBS-C: Laxatives such as macrogols (polyethylene glycol); linaclotide (guanylate cyclase-C agonist) for refractory cases; note that lactulose is not recommended as it may worsen bloating
For abdominal pain: Antispasmodics (mebeverine, peppermint oil) taken before meals
For global symptoms: Tricyclic antidepressants at low doses, with selective serotonin reuptake inhibitors (SSRIs) considered if TCAs are ineffective or not tolerated
Psychological therapies have robust evidence in IBS management, including cognitive behavioural therapy (CBT), gut-directed hypnotherapy, and mindfulness-based interventions. These address the gut-brain axis and can significantly improve quality of life. The NHS offers access to psychological therapies through NHS Talking Therapies for anxiety and depression services.
Complementary approaches such as acupuncture and reflexology should not be routinely offered for IBS treatment according to NICE guidance. The key to successful IBS management is individualised treatment, often requiring trial of multiple strategies to identify what works best for each person.
Proactive communication with your GP is essential if you have IBS and are considering GLP-1 medication, or if you develop new or worsening gastrointestinal symptoms whilst taking these medications. Several scenarios warrant medical review to ensure safe and effective management of both conditions.
Before starting GLP-1 medication, discuss your IBS history with your prescribing clinician. Inform them about:
Your IBS subtype (constipation, diarrhoea, or mixed)
Current symptom severity and frequency
Existing IBS treatments and their effectiveness
Previous responses to medications affecting gut motility
Impact of IBS on your quality of life
This information helps clinicians make informed decisions about whether GLP-1 therapy is appropriate and how to monitor you effectively.
During GLP-1 treatment, contact your GP if you experience:
Severe or persistent abdominal pain, particularly if different in character from your usual IBS symptoms or if radiating to your back (which may indicate pancreatitis—stop the medication and seek urgent medical attention)
Significant worsening of diarrhoea or constipation that doesn't improve with standard measures
Persistent nausea or vomiting affecting your ability to maintain adequate nutrition and hydration
New symptoms such as rectal bleeding, unintentional weight loss (beyond expected therapeutic effect), or nocturnal symptoms waking you from sleep
Difficulty distinguishing between IBS symptoms and medication side effects
Sudden pain in the upper right abdomen, fever, or yellowing of the skin/eyes (possible gallbladder disease—seek urgent medical attention)
Red flag symptoms requiring urgent medical attention include:
Severe, unremitting abdominal pain
Rectal bleeding or black, tarry stools
Unexplained weight loss
Persistent vomiting with inability to keep fluids down
Signs of dehydration
Your GP may arrange appropriate investigations such as blood tests (full blood count, inflammatory markers, coeliac serology) or faecal calprotectin testing to distinguish IBS from inflammatory bowel disease where appropriate. For women aged 50 or over with new IBS-type symptoms, ovarian cancer should be considered and CA125 testing may be arranged.
Your GP can assess whether symptoms represent expected medication side effects, IBS exacerbation, or potentially a different condition requiring investigation. They may adjust your GLP-1 dose, optimise your IBS management, or arrange specialist referral to a dietitian or gastroenterologist if symptoms are refractory. Regular review appointments during the first few months of GLP-1 treatment are advisable for patients with pre-existing IBS to ensure both conditions are optimally managed and to maintain quality of life.
No, GLP-1 receptor agonists are not licensed or recommended for treating IBS. They are approved only for type 2 diabetes and weight management in the UK.
GLP-1 medications commonly cause gastrointestinal side effects such as nausea, diarrhoea, constipation, and bloating, which may overlap with or potentially worsen existing IBS symptoms. Close monitoring with your GP is essential.
Contact your GP if you experience significant worsening of diarrhoea or constipation, persistent nausea or vomiting, or severe abdominal pain. Your doctor can adjust your treatment or arrange appropriate investigations.
The health-related content published on this site is based on credible scientific sources and is periodically reviewed to ensure accuracy and relevance. Although we aim to reflect the most current medical knowledge, the material is meant for general education and awareness only.
The information on this site is not a substitute for professional medical advice. For any health concerns, please speak with a qualified medical professional. By using this information, you acknowledge responsibility for any decisions made and understand we are not liable for any consequences that may result.
Lorem ipsum dolor sit amet, consectetur adipiscing elit, sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. Ut enim ad minim veniam, quis nostrud exercitation ullamco laboris nisi ut aliquip ex ea commodo consequat. Duis aute irure dolor in reprehenderit in voluptate velit esse cillum dolore eu fugiat nulla pariatur.
Block quote
Ordered list
Unordered list
Bold text
Emphasis
Superscript
Subscript