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

Can you take Wegovy and Adderall together? Many patients prescribed semaglutide for weight management alongside stimulant medications for ADHD have this important question. In the UK, Adderall is not licensed; instead, lisdexamfetamine (Elvanse) and dexamfetamine are the approved ADHD stimulants. Whilst there is no known clinically significant pharmacokinetic interaction between semaglutide and amphetamine-based medications, combining these treatments requires careful medical supervision. Both medications affect appetite, cardiovascular function, and metabolic processes in distinct ways. This article explores how these medications work, potential considerations when used together, and essential monitoring guidance to help you understand your treatment safely.
Summary: There is no known clinically significant pharmacokinetic interaction between Wegovy (semaglutide) and ADHD stimulants, but combining them requires careful medical supervision due to overlapping effects on appetite and cardiovascular function.
Many patients prescribed both Wegovy (semaglutide) for weight management and stimulant medications for attention deficit hyperactivity disorder (ADHD) understandably question whether these medications can be taken safely together. It's important to note that Adderall (mixed amphetamine salts) is not licensed in the UK; instead, UK-licensed ADHD stimulants include lisdexamfetamine (Elvanse) and dexamfetamine.
According to UK medicines information sources, there is no known clinically significant pharmacokinetic interaction between semaglutide and amphetamine-based medications. However, this does not mean these medications can be combined without careful consideration. Both drugs affect different physiological systems and can influence appetite, cardiovascular function, and metabolic processes in distinct ways. Additionally, semaglutide's effect on delaying gastric emptying may potentially affect the absorption of oral medications, including modified-release stimulant formulations.
Wegovy is a glucagon-like peptide-1 (GLP-1) receptor agonist used for chronic weight management in adults with obesity or overweight with weight-related comorbidities. In the UK, NICE guidance (TA875) recommends semaglutide only within specialist weight management services for specific patient groups. ADHD stimulants are central nervous system stimulants prescribed according to NICE guidance (NG87).
The decision to use these medications together should always be made by your prescribing clinician, who can assess your individual medical history, current health status, and treatment goals. Self-adjusting doses or combining medications without medical supervision can lead to unforeseen complications. Your GP or specialist will consider factors such as your cardiovascular health, psychiatric history, and response to each medication individually before determining whether concurrent use is appropriate for you.
This article provides educational information about how these medications work, potential considerations when used together, and guidance on monitoring your health if prescribed both treatments.
Understanding the distinct mechanisms of action for Wegovy and ADHD stimulants helps clarify why careful monitoring is important when these medications are used together.
Wegovy (semaglutide) is a long-acting GLP-1 receptor agonist administered via weekly subcutaneous injection. It mimics the action of naturally occurring GLP-1, a hormone released by the intestine in response to food intake. Semaglutide works through several mechanisms:
Appetite regulation: It acts on receptors in the brain's appetite centres, particularly the hypothalamus, reducing hunger and increasing feelings of fullness
Gastric emptying: It slows the rate at which food leaves the stomach, prolonging satiety
Glucose regulation: It enhances insulin secretion when blood glucose is elevated and suppresses inappropriate glucagon release
The medication reaches steady-state concentrations after approximately 4–5 weeks of regular dosing, with a half-life of about one week.
ADHD stimulants such as lisdexamfetamine and dexamfetamine (UK-licensed alternatives to Adderall) act as central nervous system stimulants. Their mechanisms include:
Neurotransmitter release: They increase the release of dopamine and noradrenaline in the brain
Reuptake inhibition: They block the reuptake of these neurotransmitters, prolonging their activity
Cognitive enhancement: In ADHD, they improve attention, focus, and impulse control
Appetite suppression: As a secondary effect, they typically reduce appetite through central mechanisms
Cardiovascular stimulation: They increase heart rate and blood pressure through sympathetic nervous system activation
Lisdexamfetamine is a prodrug that is converted to dexamfetamine in the body and provides a longer duration of action (typically up to 14 hours), while dexamfetamine is available in immediate-release tablets (lasting 3-5 hours).
While these medications work through separate pathways, their effects can overlap, particularly regarding appetite suppression and cardiovascular stimulation. Additionally, semaglutide's delay of gastric emptying could potentially affect the absorption profile of oral medications, including modified-release stimulant formulations.

Whilst there is no known clinically significant pharmacokinetic interaction between semaglutide and amphetamine-based medications—meaning neither medication significantly affects how the other is metabolised or eliminated from the body—there are important pharmacodynamic considerations (how the drugs' effects may overlap or compound).
Appetite suppression represents the most significant overlapping effect. Both medications reduce appetite through different mechanisms: Wegovy through GLP-1-mediated satiety signals and delayed gastric emptying, and stimulants through central effects on appetite centres. When combined, patients may experience:
Markedly reduced food intake, potentially leading to inadequate nutrition
Difficulty consuming sufficient calories to maintain healthy body function
Increased risk of nutrient deficiencies if dietary intake becomes severely restricted
Challenges in maintaining adequate hydration
Cardiovascular considerations also warrant attention. ADHD stimulants increase heart rate and blood pressure as part of their stimulant profile, whilst Wegovy typically has a modest effect on heart rate (average increase of 1–4 beats per minute). The combined effect requires monitoring, particularly in patients with pre-existing cardiovascular conditions, hypertension, or arrhythmias.
Gastrointestinal effects may be compounded. Wegovy commonly causes nausea, particularly during dose escalation, whilst stimulants can cause gastrointestinal upset in some individuals. The combination might intensify these symptoms, though this varies considerably between patients.
Medication absorption may be affected. Semaglutide's delay of gastric emptying could potentially alter the absorption profile of oral medications, including modified-release stimulant formulations. This might affect the onset or duration of the stimulant's effects, requiring clinical monitoring and possible dose timing adjustments.
Weight loss trajectory may be affected when both medications are used together, as their combined appetite-suppressant effects could lead to more rapid weight reduction than with Wegovy alone. Whilst this might seem desirable, excessively rapid weight loss (generally defined as more than 0.5–1 kg per week after the initial period) can be associated with gallstone formation, muscle loss, and nutritional deficiencies. Your healthcare provider should monitor your weight loss rate and adjust treatment accordingly.
When taking Wegovy and ADHD stimulants together, awareness of each medication's side effect profile becomes particularly important, as some adverse effects may be more pronounced or difficult to distinguish.
Common side effects of Wegovy include:
Nausea and vomiting (particularly during dose titration)
Diarrhoea or constipation
Abdominal pain or discomfort
Fatigue and dizziness
Injection site reactions
Common side effects of ADHD stimulants include:
Decreased appetite and weight loss
Insomnia and sleep disturbances
Dry mouth
Increased heart rate and blood pressure
Anxiety, nervousness, or restlessness
Headache
Practical safety measures when using both medications:
Monitor nutritional intake carefully: Keep a food diary to ensure you're consuming adequate calories and nutrients. Aim for nutrient-dense foods even if appetite is reduced.
Stay well hydrated: Both medications can affect fluid balance. Aim for at least 1.5–2 litres of water daily unless otherwise advised.
Regular cardiovascular monitoring: Have your blood pressure and heart rate checked regularly, particularly in the first few months of combined therapy.
Gradual dose titration: Wegovy is initiated at a low dose (0.25 mg weekly) and gradually increased. This titration schedule should be followed carefully when taking stimulants concurrently.
Timing considerations: Some patients find taking stimulants earlier in the day and Wegovy at a consistent time each week helps manage side effects, though there's no pharmacological requirement for specific timing.
Serious but rare risks requiring immediate medical attention (call 999 or go to A&E if severe) include:
Severe, persistent abdominal pain (potential pancreatitis)
Signs of gallbladder problems (pain in upper right abdomen, fever, yellowing of skin or eyes)
Chest pain, severe palpitations, or shortness of breath
Severe mood changes or psychotic symptoms (more commonly associated with stimulants)
Signs of severe dehydration or acute kidney injury
Patients with pre-existing conditions require particular caution, including those with cardiovascular disease, history of pancreatitis, gallbladder disease, eating disorders, psychiatric conditions, or substance use history. People with diabetes using semaglutide should be aware of potential diabetic retinopathy complications and follow ophthalmological monitoring recommendations.
Pregnancy and breastfeeding: Semaglutide should not be used during pregnancy and should be discontinued at least two months before a planned pregnancy. Effective contraception is advised for women of childbearing potential using semaglutide. Discuss family planning with your healthcare provider if taking either medication.
Open communication with your healthcare team is essential when taking multiple medications that affect weight, appetite, and metabolism. You should contact your GP or prescriber if:
You experience significant difficulty eating or maintaining adequate nutrition
Your weight loss exceeds 0.5–1 kg per week consistently after the initial treatment period
You develop persistent nausea, vomiting, or abdominal pain
You notice significant changes in heart rate, palpitations, or blood pressure readings
Sleep disturbances worsen or become unmanageable
You experience mood changes, increased anxiety, or depression
Side effects from either medication become intolerable
You're considering adjusting the dose of either medication
You are planning a pregnancy or become pregnant
Before starting combined therapy, ensure your prescriber is aware of:
Your complete medication list, including over-the-counter medicines and supplements
Your full medical history, particularly cardiovascular, gastrointestinal, and psychiatric conditions
Any history of eating disorders or disordered eating patterns
Previous responses to appetite-suppressant medications
Your weight management goals and expectations
Family planning and contraception needs
Regular monitoring appointments are important for assessing:
Weight loss trajectory and body composition changes
Nutritional status and dietary adequacy
Cardiovascular parameters (blood pressure, heart rate)
Mental health and wellbeing
Effectiveness of ADHD management
Blood glucose levels (particularly if you have diabetes or prediabetes)
Liver and kidney function as clinically indicated
NICE guidance on obesity management (TA875) and ADHD (NG87) emphasises the importance of comprehensive care. If you're taking Wegovy on the NHS, you should be enrolled in a specialist weight management service that includes dietary advice, physical activity support, and behavioural strategies. Discuss with your healthcare team how your ADHD medication might affect your engagement with these lifestyle components.
If you experience any suspected adverse reactions to either medication, you can report them through the MHRA Yellow Card scheme (yellowcard.mhra.gov.uk or the Yellow Card app).
Finally, never discontinue either medication abruptly without medical guidance. Wegovy can be stopped without tapering, but sudden cessation may lead to return of appetite and potential weight regain. Stimulant discontinuation should be discussed with your prescriber, as abrupt cessation can cause withdrawal symptoms. Your healthcare team can provide personalised advice on managing your treatment regimen safely and effectively.
There is no known clinically significant pharmacokinetic interaction between semaglutide and amphetamine-based ADHD medications. However, both medications suppress appetite and may affect cardiovascular function, requiring careful medical supervision and monitoring when used together.
You should monitor your nutritional intake, hydration, weight loss rate (ideally 0.5–1 kg per week after initial treatment), blood pressure, heart rate, and any gastrointestinal or cardiovascular symptoms. Regular appointments with your prescriber are essential for comprehensive monitoring.
Yes, the combined appetite-suppressant effects may lead to more rapid weight reduction than with Wegovy alone. Excessively rapid weight loss can increase risks of gallstones, muscle loss, and nutritional deficiencies, so your healthcare provider should monitor your weight loss trajectory and adjust treatment accordingly.
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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