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Victoza (liraglutide) is a GLP-1 receptor agonist licensed in the UK for managing type 2 diabetes in adults and adolescents aged 10 and above. Whilst its primary purpose is to improve blood glucose control, many patients experience modest weight loss as a secondary benefit. Clinical trials show that people taking Victoza 1.8 mg typically lose between 2 to 3 kg over 26 to 52 weeks. However, individual results vary considerably, and weight reduction should be viewed as an additional benefit rather than the main treatment goal. Understanding what to expect can help patients and healthcare professionals set realistic objectives for diabetes management.
Summary: Most people taking Victoza for type 2 diabetes experience modest weight loss, typically 2 to 3 kg over 6 to 12 months, though individual results vary considerably.
Victoza (liraglutide) is a prescription medicine licensed in the UK for the treatment of type 2 diabetes mellitus in adults and adolescents aged 10 years and above. It belongs to a class of medications called glucagon-like peptide-1 (GLP-1) receptor agonists, which work by mimicking the action of a naturally occurring hormone in the body.
The mechanism of action involves several complementary effects:
Stimulating insulin secretion when blood glucose levels are elevated, helping to lower blood sugar after meals
Suppressing glucagon release, which reduces glucose production by the liver
Slowing gastric emptying, meaning food moves more slowly from the stomach into the small intestine
Acting on appetite centres in the brain, which can reduce feelings of hunger and increase satiety
Victoza is administered as a once-daily subcutaneous injection using a pre-filled pen device. The dose is typically started at 0.6 mg daily and gradually increased to the maintenance dose of 1.2 mg or 1.8 mg, depending on individual response and tolerability. This gradual titration helps minimise gastrointestinal side effects.
Whilst Victoza's primary indication is glycaemic control in type 2 diabetes, many patients do experience weight loss as a secondary benefit. This occurs largely through the appetite-suppressing and gastric-slowing effects of the medication. It is important to note that in the UK, liraglutide is also available at a higher dose (3.0 mg) under the brand name Saxenda, which is specifically licensed for weight management in adults with a BMI ≥30 kg/m², or ≥27 kg/m² with weight-related comorbidities, and in adolescents with specific criteria. However, Victoza at diabetes doses (up to 1.8 mg) is not formally licensed as a weight-loss treatment, though weight reduction is a recognised clinical effect.
Clinical trial data suggests that modest weight loss is a common outcome for people taking Victoza for type 2 diabetes. However, the amount varies considerably between individuals, and it is important to maintain realistic expectations.
Clinical trial findings from the LEAD (Liraglutide Effect and Action in Diabetes) programme showed that patients taking Victoza 1.8 mg typically lost between 2 to 3 kg (approximately 4 to 7 pounds) over 26 to 52 weeks, compared to those on placebo or other diabetes medications. Some individuals experienced greater weight loss, whilst others saw minimal change or even slight weight gain.
Key points about weight loss on Victoza:
Weight loss tends to be gradual and modest rather than dramatic
Most weight loss occurs within the first 6 to 12 months of treatment
The effect appears to plateau after this initial period
Weight loss may be maintained while treatment continues, but can vary between individuals
Results are typically better when combined with lifestyle modifications including dietary changes and increased physical activity
It is crucial to understand that Victoza is not primarily a weight-loss medication at the doses used for diabetes management. The weight reduction observed is considered a beneficial side effect rather than the main therapeutic goal. Patients prescribed Victoza should focus primarily on its intended purpose: improving blood glucose control in type 2 diabetes. Any weight loss should be viewed as an additional benefit that may help improve overall metabolic health and diabetes management.
The degree of weight loss experienced on Victoza varies significantly between individuals due to multiple interacting factors. Understanding these variables can help set appropriate expectations and optimise outcomes.
Baseline characteristics play an important role:
Starting weight: People with higher initial body weight may experience greater absolute weight loss
Dose: Higher doses (1.8 mg vs 1.2 mg) are generally associated with slightly greater weight reduction
Duration of diabetes: Longer-standing diabetes may be associated with different metabolic responses
Concurrent medications: Some diabetes medications (such as insulin or sulphonylureas) can promote weight gain, potentially offsetting Victoza's weight-reducing effects and increasing hypoglycaemia risk
Lifestyle factors are equally critical:
Dietary habits: Victoza works synergistically with calorie reduction and healthier food choices
Physical activity levels: Regular exercise enhances weight loss and improves insulin sensitivity
Sleep quality and stress: Both can influence appetite hormones and weight regulation
Adherence to treatment: Consistent daily dosing is essential for optimal effect
Individual response variation also matters. People respond differently to the appetite-suppressing effects of Victoza, with some experiencing significant reduction in hunger or increased feelings of fullness, while others notice minimal impact on appetite.
Tolerability and side effects can indirectly affect weight outcomes. Gastrointestinal symptoms such as nausea, which are common especially during dose escalation, may temporarily reduce appetite and food intake. However, these effects typically diminish over time as the body adjusts to the medication.
When starting Victoza, it is essential to maintain a balanced perspective on treatment goals. Whilst weight loss can be a welcome benefit, the primary objective remains optimising glycaemic control and reducing long-term diabetes complications.
The primary purpose of Victoza in type 2 diabetes management is to:
Lower HbA1c (a measure of average blood glucose over 2-3 months)
Reduce fasting and post-meal blood glucose levels
Additionally, clinical evidence from the LEADER trial has shown that liraglutide can reduce the risk of major cardiovascular events in people with type 2 diabetes who have established cardiovascular disease.
According to NICE guidance (NG28), GLP-1 receptor agonists like Victoza are typically considered for adults with type 2 diabetes when:
Metformin and other oral medications have not achieved adequate glycaemic control
The person has a BMI of 35 kg/m² or higher (or lower with specific circumstances)
Weight loss would benefit other significant obesity-related comorbidities
Importantly, NICE recommends continuing GLP-1 receptor agonist treatment only if there is a beneficial metabolic response (a reduction in HbA1c of at least 11 mmol/mol [1%] and weight loss of at least 3% of initial body weight in 6 months).
Setting realistic expectations is crucial for treatment satisfaction and adherence. Patients should understand that:
Weight loss, if it occurs, will likely be modest (typically 2-5% of body weight)
The medication is not a substitute for lifestyle modifications
Blood sugar improvements may occur independently of weight changes
Some people may not lose weight at all, yet still achieve excellent diabetes control
Discontinuing the medication typically results in weight regain and worsening glycaemic control
Healthcare professionals should emphasise that successful diabetes management encompasses multiple outcomes beyond the number on the scales, including improved energy levels, better blood glucose stability, reduced medication burden, and decreased risk of long-term complications.
Regular communication with your healthcare team is essential when taking Victoza, particularly regarding weight changes and overall treatment response. Certain situations warrant prompt medical review.
Contact your GP or diabetes specialist nurse if you experience:
Unexpected or rapid weight loss (more than 1-2 kg per week) that seems excessive or is accompanied by other symptoms
No improvement in blood glucose control after 3-6 months of treatment at the maximum tolerated dose
Persistent gastrointestinal side effects (nausea, vomiting, diarrhoea) that interfere with eating, hydration, or quality of life
Signs of dehydration including dark urine, dizziness, or reduced urination, particularly if experiencing vomiting or diarrhoea
Seek urgent medical advice (call NHS 111, urgent care or emergency services) and stop taking Victoza if you experience:
Severe, persistent abdominal pain, especially if radiating to the back, which could indicate pancreatitis (a rare but serious side effect)
Right-sided upper abdominal pain, fever or yellowing of the skin/eyes, which could indicate gallbladder problems
Contact your healthcare team promptly if you experience:
Routine monitoring is also important. Your healthcare team will typically:
Review your HbA1c levels every 3-6 months to assess diabetes control
Monitor weight and BMI at regular appointments
Assess kidney function periodically (no dose adjustment is required in renal impairment, though caution is advised in severe renal impairment)
Discuss any changes in other medications that might affect weight or blood glucose
If weight loss is insufficient or you have concerns about your diabetes management, your GP may consider:
Reviewing your overall diabetes treatment plan
Referring you to a dietitian for specialist nutritional advice
Discussing whether alternative or additional medications might be appropriate
Assessing whether referral to specialist weight management services is suitable
Remember that diabetes management is individualised, and what works well for one person may differ for another. Open, ongoing dialogue with your healthcare team ensures your treatment remains optimally tailored to your needs.
If you suspect you've experienced a side effect from Victoza, you can report it through the MHRA Yellow Card Scheme at yellowcard.mhra.gov.uk.
Victoza (liraglutide up to 1.8 mg) is licensed in the UK for type 2 diabetes management, not specifically for weight loss. However, liraglutide at a higher dose (3.0 mg) is available as Saxenda, which is licensed for weight management in adults with a BMI ≥30 kg/m² or ≥27 kg/m² with weight-related comorbidities.
Most weight loss on Victoza occurs within the first 6 to 12 months of treatment. The effect is gradual and modest, typically plateauing after this initial period, though weight may be maintained whilst treatment continues.
Discontinuing Victoza typically results in weight regain and worsening glycaemic control. The medication's effects on appetite, gastric emptying, and blood glucose regulation diminish once treatment is stopped, so maintaining lifestyle modifications remains important.
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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