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

Mounjaro (tirzepatide) is a dual GIP and GLP-1 receptor agonist licensed in the UK for treating type 2 diabetes in adults. Whilst common side effects include nausea, vomiting, and gastrointestinal discomfort, some patients wonder whether Mounjaro can cause nightmares or sleep disturbances. Nightmares are not listed as a recognised adverse effect in the MHRA Summary of Product Characteristics or clinical trial data. However, individual experiences vary, and understanding potential indirect factors—such as blood glucose fluctuations, gastrointestinal symptoms, or concurrent medications—is important for patients and healthcare professionals managing diabetes treatment safely and effectively.
Summary: Nightmares are not a recognised side effect of Mounjaro (tirzepatide) according to MHRA and EMA regulatory data or clinical trials.
Mounjaro (tirzepatide) is a prescription medicine licensed in the UK for the treatment of type 2 diabetes mellitus in adults. It belongs to a class of medications known as dual glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptor agonists. By mimicking the action of these naturally occurring hormones, Mounjaro helps to regulate blood sugar levels, enhance insulin secretion when glucose is elevated, and slow gastric emptying. This mechanism improves glycaemic control and may contribute to weight loss in many patients with type 2 diabetes.
As with all medications, Mounjaro can cause side effects, though not everyone will experience them. The most commonly reported adverse effects according to the MHRA Summary of Product Characteristics (SmPC) include:
Gastrointestinal effects: nausea, vomiting, diarrhoea, constipation, abdominal pain, decreased appetite, dyspepsia (indigestion), eructation (belching)
Injection site reactions: redness, swelling or irritation
Fatigue
These symptoms are typically mild to moderate and often diminish as the body adjusts to the medication, particularly during the initial dose-escalation phase.
More serious side effects can include pancreatitis, gallbladder problems, and hypoglycaemia (especially when used alongside other glucose-lowering medications such as sulphonylureas or insulin).
Important safety information: Seek urgent medical attention if you experience severe, persistent abdominal pain (with or without vomiting), yellowing of the skin or eyes (jaundice), signs of a severe allergic reaction (rash, swelling, difficulty breathing), or persistent vomiting/diarrhoea causing dehydration.
The MHRA SmPC and patient information leaflet do not list nightmares or vivid dreams as recognised side effects of Mounjaro. However, patients may report a wide range of experiences during treatment, and understanding the broader context of sleep disturbances is essential for both patients and healthcare professionals.

Nightmares are not a recognised adverse effect in the MHRA SmPC or European Medicines Agency (EMA) assessment report for Mounjaro (tirzepatide) as of May 2024. The SURPASS clinical trial programme, which evaluated tirzepatide in thousands of patients with type 2 diabetes, did not report nightmares as a significant treatment-emergent adverse event.
That said, individual patient experiences can vary, and some people taking Mounjaro may report changes in their sleep patterns or dream content. It is important to distinguish between a direct pharmacological effect of the medication and other factors that might influence sleep quality. Sleep disturbances, including nightmares, can arise from numerous causes unrelated to a specific medication, such as stress, anxiety, concurrent illness, or other medications.
Post-marketing surveillance and patient feedback continue to inform our understanding of any medication's safety profile. If a pattern of sleep-related side effects were to emerge in real-world use, regulatory authorities such as the MHRA and the EMA would investigate and update guidance accordingly.
For patients concerned about nightmares or unusual dreams while taking Mounjaro, it is crucial to discuss these symptoms with a GP or diabetes specialist. A thorough assessment can help determine whether the sleep disturbance is coincidental, related to another factor, or potentially linked to the medication.
While nightmares are not a recognised side effect of Mounjaro, several indirect mechanisms could potentially contribute to sleep disturbances in some individuals. Understanding these factors can help patients and clinicians identify and address potential causes.
Gastrointestinal side effects, particularly nausea and abdominal discomfort, are common with Mounjaro, especially during the initial weeks of treatment or following dose increases. Persistent nausea or discomfort at night may disrupt sleep quality and potentially influence dream recall. Individuals who experience significant gastrointestinal symptoms may find their sleep fragmented, leading to more frequent awakenings during REM (rapid eye movement) sleep—the stage most associated with vivid dreaming.
Blood glucose fluctuations may also play a role. Although Mounjaro is designed to improve glycaemic control, some patients—particularly those on combination therapy—may experience episodes of hypoglycaemia (low blood sugar). According to Diabetes UK resources, nocturnal hypoglycaemia can cause night sweats, palpitations, and may be associated with disturbed sleep or vivid dreams. Conversely, hyperglycaemia (high blood sugar) can also affect sleep quality.
Weight loss and metabolic changes associated with Mounjaro treatment may influence sleep patterns. Changes in diet, energy balance or weight may sometimes affect sleep quality, though direct effects on dream intensity are not well established.
Finally, it is worth considering concurrent medications. Many individuals with type 2 diabetes take multiple medications, some of which may affect sleep. For example, certain beta-blockers have been reported to cause sleep disturbances or nightmares in some patients according to their SmPCs, while some statins have rare reports of sleep effects. A comprehensive medication review can help identify potential contributors to sleep-related symptoms.
If you are taking Mounjaro and experiencing nightmares or other sleep disturbances, there are several practical steps you can take to address the issue and ensure your safety and wellbeing.
Contact your GP or diabetes specialist to discuss your symptoms. They can conduct a thorough assessment to explore possible causes and determine the most appropriate course of action. Generally, you should not stop taking Mounjaro without consulting your healthcare professional, as abrupt discontinuation of diabetes medication can lead to poor glycaemic control.
However, seek urgent medical attention (call 999 or go to A&E) if you experience:
Severe, persistent abdominal pain (with or without vomiting) – which could indicate pancreatitis
Signs of a severe allergic reaction (rash, swelling, difficulty breathing)
Severe, persistent vomiting or diarrhoea causing dehydration
Yellowing of the skin or eyes (jaundice)
For less urgent concerns, your healthcare provider may:
Review your current medications to identify any other drugs that might contribute to sleep disturbances
Assess your blood glucose control, including checking for nocturnal hypoglycaemia
Evaluate gastrointestinal symptoms and consider dose adjustments or supportive treatments to minimise nausea and discomfort
Screen for co-existing conditions such as sleep apnoea, anxiety, or depression that may require separate management
If you suspect nocturnal hypoglycaemia (symptoms include sweating, trembling, confusion upon waking), check your blood glucose if possible. Treat low blood glucose (below 4 mmol/L) with a fast-acting carbohydrate such as glucose tablets or fruit juice, following NHS guidance. Discuss with your healthcare team if you need adjustment of insulin or sulphonylurea doses.
Practical self-care measures can also support better sleep quality:
Maintain good sleep hygiene: establish a regular sleep schedule, create a comfortable sleep environment, and avoid screens before bedtime
Keep a symptom diary noting when nightmares occur, their frequency, and any associated factors
Avoid heavy meals close to bedtime to reduce gastrointestinal discomfort
If nightmares are severe, persistent, or significantly affecting your quality of life, your doctor may consider adjusting your Mounjaro dose or switching to an alternative medication.
Safety reporting: You can report any suspected side effects via the MHRA Yellow Card Scheme at www.mhra.gov.uk/yellowcard, contributing valuable information to ongoing drug safety monitoring.
No, nightmares are not listed as a recognised adverse effect in the MHRA Summary of Product Characteristics or clinical trial data for Mounjaro (tirzepatide).
Contact your GP or diabetes specialist to discuss your symptoms. They can assess potential causes such as blood glucose fluctuations, gastrointestinal discomfort, or other medications, and determine the most appropriate course of action.
Yes, nocturnal hypoglycaemia (low blood sugar) can cause night sweats, palpitations, and disturbed sleep or vivid dreams, particularly in patients taking Mounjaro alongside insulin or sulphonylureas.
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.
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