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Can you inject Saxenda in your bum? This is a common question among patients prescribed this GLP-1 receptor agonist for weight management. Saxenda (liraglutide 3.0 mg) is a once-daily subcutaneous injection licensed in the UK for adults with obesity or overweight with comorbidities. Proper injection technique and site selection are essential for treatment safety and effectiveness. The buttocks are not an approved injection site according to UK prescribing information. This article explains the recommended injection sites, correct administration technique, and why following manufacturer guidance matters for optimal therapeutic outcomes.
Summary: No, the buttocks are not an approved injection site for Saxenda according to UK prescribing information and manufacturer guidance.
Saxenda (liraglutide 3.0 mg) is a once-daily subcutaneous injection licensed in the UK for weight management in adults with a body mass index (BMI) of 30 kg/m² or greater, or 27 kg/m² or greater in the presence of weight-related comorbidities. It is also approved for adolescents aged 12 years and older with a body weight above 60 kg and obesity. As a glucagon-like peptide-1 (GLP-1) receptor agonist, Saxenda works by mimicking the action of the naturally occurring hormone GLP-1, which regulates appetite and food intake. The medication slows gastric emptying, increases feelings of fullness, and reduces hunger signals to the brain, thereby supporting calorie reduction when combined with a reduced-calorie diet and increased physical activity.
The effectiveness and safety of Saxenda depend not only on consistent daily administration but also on proper injection technique. Subcutaneous injections deliver medication into the fatty tissue layer beneath the skin, where it is gradually absorbed into the bloodstream. The choice of injection site matters because different areas of the body have varying amounts of subcutaneous fat, blood flow patterns, and sensitivity levels. Using the correct injection sites as specified by the manufacturer and the Medicines and Healthcare products Regulatory Agency (MHRA) helps ensure predictable drug absorption, minimises discomfort, and reduces the risk of injection-site reactions such as bruising, redness, or itching.
Understanding where and how to inject Saxenda is fundamental to treatment success. Patients should receive comprehensive training from their prescribing healthcare professional or practice nurse before starting treatment. This training typically covers injection technique, site rotation, needle safety, and storage requirements. Proper education empowers patients to self-administer their medication confidently and safely at home.

The short answer is no — the buttocks are not a recommended injection site for Saxenda according to the manufacturer's instructions and UK prescribing information. Whilst the buttocks contain subcutaneous tissue and are used for some other types of injections, they are not included in the recommended sites for Saxenda administration in the Summary of Product Characteristics (SmPC).
The approved injection sites for Saxenda have been specifically studied during clinical development. Using alternative sites that haven't been evaluated could potentially alter how the medication is absorbed. Additionally, the buttocks can be difficult to reach for self-injection, increasing the risk of incorrect technique or inadequate subcutaneous depth. Patients may also have difficulty visualising the injection site on their buttocks, making proper site rotation and inspection for adverse reactions more challenging.
Using injection sites not recommended in the SmPC would constitute off-label use. Patients who find the approved injection sites uncomfortable or unsuitable should discuss their concerns with their GP or prescribing clinician rather than experimenting with alternative sites. Healthcare professionals can provide guidance on technique refinement, site rotation strategies, or address any underlying issues that may be making injections difficult.
Importantly, do not inject Saxenda into a vein or muscle, as this has not been studied and may affect how the medication works or increase side effects.
Saxenda should be injected subcutaneously in one of three approved body areas: the abdomen (tummy), the front of the thighs, or the upper arms. These sites have been specifically validated through clinical research and are recommended in the Summary of Product Characteristics (SmPC) approved by the MHRA and European Medicines Agency (EMA).
The abdomen is often the most convenient and commonly used site. Injections should avoid the area directly around the belly button. The abdomen typically has good subcutaneous fat coverage and is easily accessible for self-injection. Patients should avoid injecting into areas with scars, bruises, or skin abnormalities.
The front of the thighs provides another suitable option, particularly the outer and front aspects of the upper thigh. This area is easily accessible when sitting and offers adequate subcutaneous tissue in most individuals. Patients should avoid the inner thigh and areas too close to the knee or groin.
The upper arms can be used, specifically the outer back portion of the upper arm where there is sufficient subcutaneous fat. However, this site can be more challenging for self-injection and may require assistance from a family member or carer to ensure proper technique. Some patients find it difficult to pinch the skin adequately in this area.
Site rotation is essential to reduce injection-site reactions such as redness, itching, bruising, or pain. Patients should rotate between different areas and, within each area, use different spots for each injection. A systematic rotation pattern — for example, using the abdomen for morning injections one week, then switching to the thighs the following week — helps distribute the injection load across multiple sites. Keeping a simple diary or using the same site on the same day of the week can help establish a rotation routine.
Proper injection technique is crucial for ensuring Saxenda's effectiveness and minimising adverse effects. Before each injection, patients should wash their hands thoroughly with soap and water. The Saxenda pen should be inspected to ensure the solution is clear and colourless; any cloudiness, discolouration, or particles indicate the medication should not be used.
Preparing the injection site involves cleaning the chosen area with an alcohol wipe if recommended by your healthcare provider, though this is not always necessary for home injections if the skin is visibly clean. Allow the skin to dry completely before injecting. Attach a new needle to the pen for each injection — needles should never be reused as this increases infection risk and can damage the pen mechanism.
The injection process involves the following steps:
Select your injection site and ensure you're using a different spot from your last injection
Pinch a fold of skin gently between your thumb and forefinger to lift the subcutaneous tissue away from underlying muscle
Insert the needle at a 90-degree angle (straight in) with a quick, dart-like motion
Press the dose button fully and hold it down whilst keeping the needle in the skin
Count slowly to six to ensure the full dose is delivered
Release the dose button and withdraw the needle at the same angle it was inserted
Do not rub the injection site afterwards
After injection, use the outer needle cap to safely remove the needle from the pen and dispose of it immediately in a sharps container. Do not recap with the inner cap as this increases needlestick injury risk. The Saxenda pen should be stored without a needle attached, with the pen cap replaced to protect from light, and kept in a refrigerator (2°C to 8°C) before first use. Once in use, the pen can be stored below 30°C or in a refrigerator for up to one month. Never freeze Saxenda and never share your pen with others.
For sharps disposal, contact your local council's clinical waste service or ask your community pharmacy about their sharps disposal scheme. Perform a flow check before using a new pen for the first time.
Patients experiencing persistent pain, difficulty injecting, or injection-site reactions should contact their GP or practice nurse for technique review and support. Report any suspected side effects via the MHRA Yellow Card Scheme (yellowcard.mhra.gov.uk).
Using an unapproved injection site for Saxenda, such as the buttocks, may lead to several potential issues, though the severity and likelihood vary between individuals. The primary concern is altered drug absorption, which could possibly affect how much liraglutide enters your bloodstream and how quickly it does so. Different body areas have varying blood flow, fat distribution, and tissue characteristics that influence subcutaneous medication absorption. This could potentially result in unpredictable therapeutic effects.
Injection into muscle tissue (intramuscular injection) rather than subcutaneous fat is more likely when using sites not designed for self-administered subcutaneous injections. Intramuscular injection of Saxenda could possibly cause more rapid absorption than intended, which might affect the medication's action. It may also cause localised pain or muscle irritation.
Injection-site reactions may occur when using inappropriate sites. These can include redness, swelling, itching, bruising, or pain at the injection site. The risk of such reactions with unapproved sites is unknown as these have not been systematically studied.
If you have accidentally injected Saxenda in an unapproved site on one occasion, do not panic. Monitor yourself for any unusual symptoms, particularly increased gastrointestinal side effects or injection-site reactions. For your next dose, return to using an approved injection site. If you experience severe pain, significant swelling, signs of infection (warmth, redness, pus), or concerning systemic symptoms, contact your GP or NHS 111 for advice. Seek urgent medical help if you experience signs of a severe allergic reaction.
Going forward, ensure you understand and follow the correct injection technique. If you're finding the approved sites difficult to use, speak with your healthcare provider about strategies to make injections more comfortable or whether Saxenda remains the most suitable treatment option for you. Never modify your injection technique without professional guidance, as adherence to evidence-based administration methods is essential for both safety and treatment effectiveness.
The approved injection sites for Saxenda are the abdomen (avoiding the area around the belly button), the front of the thighs, and the upper arms. These sites have been validated through clinical research and are specified in the UK Summary of Product Characteristics.
Site rotation is essential to reduce injection-site reactions such as redness, itching, bruising, and pain. Patients should rotate between different approved areas and use different spots within each area for consecutive injections to distribute the injection load and minimise tissue irritation.
If you accidentally inject Saxenda in an unapproved site, monitor yourself for unusual symptoms or injection-site reactions. Return to using an approved site for your next dose. Contact your GP or NHS 111 if you experience severe pain, significant swelling, signs of infection, or concerning symptoms.
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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