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
 

Saxenda (liraglutide 3.0 mg) is a GLP-1 receptor agonist licensed in the UK for weight management in adults with obesity or overweight with comorbidities. Whilst there is no established causal link between Saxenda and mental health conditions, some patients have reported mood changes during treatment. The MHRA and EMA continue to monitor psychiatric adverse effects through post-marketing surveillance. This article examines the relationship between Saxenda and mental health, identifies patients who may require additional caution, and provides guidance on monitoring mental wellbeing throughout treatment. Understanding these considerations helps ensure safe, effective weight management that prioritises both physical and psychological health.
Summary: There is no established causal link between Saxenda (liraglutide) and mental health conditions, though some patients report mood changes during treatment, prompting ongoing regulatory monitoring by the MHRA and EMA.
Saxenda (liraglutide 3.0 mg) is a prescription-only injectable medicine licensed in the UK for weight management in adults with obesity (BMI ≥30 kg/m²) or overweight (BMI ≥27 kg/m²) with at least one weight-related comorbidity, such as type 2 diabetes or hypertension. It is administered once daily via subcutaneous injection and is intended to be used alongside a reduced-calorie diet and increased physical activity.
Saxenda belongs to a class of medicines called glucagon-like peptide-1 (GLP-1) receptor agonists. It works by mimicking the action of GLP-1, a naturally occurring hormone released by the intestine after eating. The mechanism of action involves several pathways: it slows gastric emptying, which prolongs the feeling of fullness after meals; it acts on appetite centres in the hypothalamus to reduce hunger and food cravings; and it helps regulate blood glucose levels by enhancing insulin secretion when blood sugar is elevated.
Clinical trials have demonstrated that Saxenda, when combined with lifestyle modifications, can lead to clinically significant weight loss. The treatment involves a weekly dose titration schedule, starting at a lower dose and gradually increasing to the full 3.0 mg dose to improve tolerability. According to NICE Technology Appraisal guidance, liraglutide 3.0 mg is recommended as an option for managing overweight and obesity in specific patient groups, typically within specialist weight management services. NHS availability is restricted to patients meeting strict eligibility criteria, with treatment reviewed after 12 weeks at the full dose and continued only if at least 5% of initial body weight has been lost.
Common side effects include gastrointestinal symptoms such as nausea, vomiting, diarrhoea, and constipation, which typically improve over time. Patients should report any suspected side effects to their healthcare professional or directly to the MHRA Yellow Card scheme (yellowcard.mhra.gov.uk). While there is no established causal link between Saxenda and mental health conditions, regulatory bodies continue to monitor reports of mood changes during treatment.
The relationship between Saxenda and mental health remains an area of ongoing clinical scrutiny. There is no established causal link between liraglutide and the development of depression or anxiety disorders, as confirmed by recent reviews by the MHRA and European Medicines Agency (EMA) Pharmacovigilance Risk Assessment Committee (PRAC). However, these regulatory bodies continue to monitor post-marketing surveillance data for potential psychiatric adverse effects.
Some patients have reported experiencing mood changes, low mood, anxiety, or depressive symptoms whilst taking Saxenda. These reports have prompted healthcare professionals to remain vigilant, particularly given that weight management itself can be emotionally challenging. It is important to recognise that individuals seeking weight loss treatment may already have underlying mental health vulnerabilities, and the process of significant lifestyle change can be psychologically demanding.
The Summary of Product Characteristics (SmPC) for Saxenda notes that mood disorders including depression have been reported in clinical practice, though with uncommon frequency. Factors that may potentially contribute to mood changes during treatment include:
The psychological impact of dietary restriction and lifestyle changes
Pre-existing mental health conditions that may fluctuate
Gastrointestinal side effects affecting quality of life and wellbeing
The emotional aspects of weight management
Individual psychological responses to body changes
Patients should be advised to monitor their mental wellbeing throughout treatment and report any concerning symptoms promptly. Healthcare professionals should conduct a thorough mental health assessment before initiating Saxenda and maintain regular follow-up. If significant mood disturbance, persistent low mood, anxiety, or suicidal ideation develops, patients should seek urgent medical advice. Treatment discontinuation should be considered while appropriate mental health support is arranged, in line with clinical judgement.
Whilst Saxenda is not absolutely contraindicated in individuals with mental health conditions, careful risk-benefit assessment is essential before prescribing to patients with current or previous psychiatric disorders. Healthcare professionals should exercise particular caution and consider alternative weight management strategies in certain circumstances.
Patients with active severe depression or those experiencing suicidal ideation would generally benefit from mental health stabilisation under appropriate psychiatric care before commencing Saxenda. The additional psychological demands of weight loss treatment may be challenging during periods of mental health vulnerability. Similarly, individuals with poorly controlled anxiety disorders or those in acute mental health crisis may require stabilisation before considering pharmacological weight management.
Those with a history of eating disorders, including anorexia nervosa, bulimia nervosa, or binge eating disorder, require specialist assessment in line with NICE guidance (NG69). The focus on weight loss and appetite suppression may potentially affect disordered eating patterns. A multidisciplinary approach involving mental health specialists, dietitians, and eating disorder services is advisable before considering Saxenda in this population.
Additional considerations include:
Patients taking psychotropic medications – while direct drug interactions are limited, Saxenda's effect on delaying gastric emptying may affect absorption of some oral medicines
Individuals with bipolar disorder, particularly during unstable phases
Those with substance use disorders, as weight loss medications require careful adherence
Patients lacking adequate mental health support networks
Before prescribing Saxenda, clinicians should:
Conduct a comprehensive mental health history
Screen for current mood disorders using validated tools
Assess suicide risk and self-harm history
Ensure appropriate mental health support is in place
Discuss potential risks openly with the patient
Arrange more frequent follow-up for vulnerable individuals
Patients should be empowered to make informed decisions, understanding that alternative weight management approaches, including psychological interventions, dietary support, and increased physical activity, may be more appropriate for their circumstances.
For patients deemed suitable for Saxenda treatment, proactive mental health monitoring is essential throughout the treatment course. A collaborative approach between the prescribing clinician, the patient, and where appropriate, mental health services, optimises both physical and psychological outcomes.
Before starting treatment, patients should be educated about potential mood-related side effects and encouraged to maintain open communication with their healthcare team. Establishing a baseline mental health assessment using standardised screening tools such as the PHQ-9 (Patient Health Questionnaire-9) for depression or GAD-7 (Generalised Anxiety Disorder-7) for anxiety provides a reference point for monitoring changes.
During treatment, patients should:
Monitor mood regularly and keep a symptom diary if helpful
Maintain regular contact with their GP or prescribing clinician, typically monthly initially
Report any concerning symptoms immediately, including persistent low mood, anxiety, irritability, or thoughts of self-harm
Continue existing mental health treatments and medications as prescribed
Engage with psychological support such as counselling or cognitive behavioural therapy (CBT) if needed
Prioritise self-care, including adequate sleep, stress management, and social connection
Ensure nutritional adequacy through balanced eating despite reduced appetite
Maintain physical activity, which has proven mental health benefits
Healthcare professionals should schedule regular review appointments to assess both weight loss progress and mental wellbeing. Treatment should be discontinued if a 5% weight loss has not been achieved after 12 weeks at the full 3.0 mg daily dose, in line with the SmPC and NICE guidance. If mood deterioration occurs, a thorough evaluation is required to determine whether symptoms are related to Saxenda, the weight loss process itself, or independent factors. Management options include:
Dose adjustment or temporary treatment pause
Enhanced psychological support or referral to mental health services
Optimisation of existing mental health treatments
Discontinuation of Saxenda if symptoms are severe or persistent
When to seek urgent help: Patients should call 999 if they are at immediate risk of harm to themselves or others. For urgent but non-life-threatening mental health concerns, they should contact NHS 111, their local NHS urgent mental health helpline, or their GP. The Samaritans (116 123) offer confidential emotional support.
Patients should report any suspected side effects to their healthcare professional or directly to the MHRA Yellow Card scheme (yellowcard.mhra.gov.uk). Successful weight management with Saxenda requires a holistic approach that prioritises mental health alongside physical health outcomes, ensuring patient safety and wellbeing remain paramount throughout treatment.
There is no established causal link between Saxenda and depression or anxiety, as confirmed by the MHRA and EMA. However, some patients report mood changes during treatment, and regulatory bodies continue to monitor psychiatric adverse effects through post-marketing surveillance.
Saxenda is not absolutely contraindicated in individuals with mental health conditions, but careful risk-benefit assessment is essential. Patients with active severe depression, suicidal ideation, poorly controlled anxiety, or eating disorders require specialist evaluation and mental health stabilisation before commencing treatment.
Report any concerning symptoms immediately to your GP or prescribing clinician, including persistent low mood, anxiety, or thoughts of self-harm. Treatment may need to be paused or discontinued whilst appropriate mental health support is arranged, and you should seek urgent help if you are at immediate risk of harm.
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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