Brain
Appetite and fullness signals
Incretin pathways influence areas of the brain involved in appetite regulation, which can reduce hunger and food-seeking between meals.
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Doctor-supervised weight management · Singapore
A medically supervised programme combining metabolic screening, individualised prescription decisions, sustainable nutrition and resistance training. The goal is to reduce biological barriers to weight management while preserving muscle and building habits that can last.

Quick answer
Semaglutide and tirzepatide are prescription-only treatments that act on gut-hormone pathways involved in appetite, satiety and glucose regulation. Tirzepatide, marketed in Singapore under the brand name Mounjaro, also acts on GIP receptors. Medication is considered only after a doctor reviews metabolic health, medical history, contraindications and treatment goals.1
Related conditions: Medical Weight Loss in Singapore, and Diabetes Care in Singapore.
Measurements, medical history, medicines, metabolic blood work and contraindication review come before any prescription.
Protein, fibre, resistance training, sleep and realistic meal structure are planned around your life.
Dose progression follows response and tolerability. Weight, waist, strength, nutrition and metabolic markers guide follow-up.
Treatment approach
Semaglutide acts on GLP-1 receptors. Tirzepatide acts on GIP and GLP-1 receptors. Both are used alongside nutrition and physical activity.
Glucose control, lipids, liver, kidney, thyroid and other relevant markers help define suitability and what to monitor.
Adequate protein, fibre, hydration and practical meal structure support satiety, training and lean-mass retention.
Progressive strength work helps preserve function and muscle while body weight changes.
Interactive assessment
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Your BMI
28.4
Obese
High risk of obesity-related conditions7
At your height, the healthy weight range is about 53 to 66 kg. This is a population screening category, not a medical diagnosis. A doctor also reviews waist measurement, medical history and metabolic results.
Eligible based on this initial screening guide
The educational threshold shown is BMI 27.5 for the selected profile. It is not a diagnosis or prescription decision. Waist measurement, metabolic markers, medical history and contraindications also matter.2
Research illustration
Trial
STEP 1
semaglutide
12.2 kg
14.9% mean reduction at 68 weeks, 1,961 adults, versus 2.4% with placebo, alongside lifestyle intervention.3
Trial
SURMOUNT-1
tirzepatide
12.3 to 17.1 kg
15.0% to 20.9% dose-group means at 72 weeks, 2,539 adults without diabetes, versus 3.1% with placebo, alongside lifestyle intervention.4
These calculations translate study-group averages into kilograms. They are not a personal forecast, target or promised range. Individual outcomes vary.
Protect the result by protecting muscle
Adequate protein, resistance training and a sustainable rate of loss support lean-mass retention. Dose progression is reviewed according to response and tolerability, not increased quickly by default.
Treatment decisions follow a doctor’s review of medical history, contraindications and baseline metabolic markers.
Waist, blood pressure, glucose, lipids, liver health, strength and body composition inform the plan.
Protein, resistance training, tolerable dose progression and maintenance planning are built into care.
In depth
These medicines act on the same receptor pathways your body uses after a meal. Select a point to see what happens where.
Brain
Incretin pathways influence areas of the brain involved in appetite regulation, which can reduce hunger and food-seeking between meals.
Stomach
Food leaves the stomach more gradually, so a meal can feel satisfying for longer. This is also why early nausea or fullness can occur.
Pancreas
Insulin release is supported when blood glucose is raised, and the response settles as glucose falls.
Gut
The gut releases incretin hormones after a meal. These medicines act on the same receptor pathways that those natural signals use.
Semaglutide acts on the GLP-1 receptor pathway. Tirzepatide acts on both the GIP and GLP-1 receptor pathways. Neither is a stimulant, and both are used alongside nutrition, activity and sleep.1
Both formats are prescription-only and are chosen with your doctor. The difference is routine and practicality, not a ranking.
One week
One week
Treatment starts low and moves only when review supports it.
Starting dose
Chosen to let the body adjust, not to produce fast change.
First review step
Adjusted only if response and tolerability support it.
Maintained dose
The lowest dose that gives a steady, workable result.
Higher doses
Considered case by case, and not an automatic goal.
The aim is the lowest dose that works for you. Dose progression follows response and tolerability rather than a fixed schedule, because a higher step is not automatically a better one. A sustainable dose still allows adequate protein, resistance training and normal daily function, which is also what supports lean-mass retention while weight changes.3
Singapore uses lower BMI action points for Asian populations because metabolic risk can rise at a lower BMI. Product-label eligibility and individual prescribing decisions remain separate, so waist circumference, related conditions and metabolic results also matter.
Weight reduction can include both fat and lean tissue. Adequate protein, progressive resistance training, a sustainable rate of loss and body-composition or strength review help keep the programme focused on function as well as scale weight.
STEP 1 and SURMOUNT-1 report averages from controlled study populations receiving structured lifestyle support. They show what happened across groups, not what any one person should expect. Starting weight, health, adherence, dose exposure and tolerability all influence outcomes.
Appetite can return after treatment stops. The STEP 1 extension found substantial regain during the following year, which supports treating weight management as long-term care rather than a short course. Maintenance planning begins before treatment starts.
Review goals, prior attempts, symptoms, medicines, eating patterns, activity, sleep and relevant history. Complete measurements and clinically indicated blood tests.
Review tolerability, nutrition, hydration, strength training, weight trajectory, waist and metabolic markers. Adjust only when the overall plan remains sustainable.
The programme starts with medical context, not a prescription request. Your doctor determines whether treatment is appropriate, your Personal Health Concierge coordinates tests and follow-ups, and the plan keeps nutrition, resistance training, sleep and long-term maintenance in view. The aim is sustainable health change with careful monitoring and no pressure to escalate quickly.
Are these medicines prescription-only?
Yes. A doctor must assess suitability before prescribing.
Is BMI enough to decide?
No. Waist, related conditions, metabolic markers, history and contraindications also matter.
Will a higher dose always work better?
Not necessarily. Response, tolerability, nutrition and function guide dose review.
Can muscle loss be prevented completely?
No guarantee is possible, but protein, resistance training and a sustainable rate of loss can support lean-mass retention.
Clear answers, written by our clinical team. Tap any question for its direct permalink, or reach out to your Personal Concierge for anything else.
As an educational guide, treatment may be considered for Asian adults at BMI 27.5 or above without a related condition, or BMI 25 or above with a condition such as diabetes or fatty liver disease. For non-Asian adults, the corresponding guide is BMI 30 or above, or BMI 27 or above with a related condition. A doctor must still assess medical history, contraindications and baseline results before any prescription.
Assessment usually covers weight, waist circumference, blood pressure, previous weight-management attempts, current medicines and relevant medical history. Blood tests may include glucose or HbA1c, lipids, liver and kidney function, and thyroid markers. The doctor also screens for contraindications and discusses pregnancy plans where relevant.
In STEP 1, adults receiving semaglutide plus lifestyle intervention lost 14.9% of starting weight on average at 68 weeks, compared with 2.4% with placebo. In SURMOUNT-1, tirzepatide dose groups lost 15.0% to 20.9% on average at 72 weeks, compared with 3.1% with placebo. These are group averages from controlled studies, not a forecast for an individual.
Semaglutide acts on the GLP-1 receptor. Tirzepatide acts on both GIP and GLP-1 receptors. Both are prescription-only, once-weekly treatments used alongside nutrition and physical activity. The appropriate option depends on medical history, treatment goals, tolerability and the doctor’s assessment.
Nausea, vomiting, diarrhoea, constipation and abdominal discomfort are among the common effects. Gradual clinician-led dose progression, smaller meals and hydration can support tolerability. Severe or persistent abdominal pain, repeated vomiting or an inability to keep fluids down requires medical review.
Treatment may be unsuitable during pregnancy or breastfeeding and for people with certain endocrine cancer histories, previous pancreatitis, severe gastrointestinal disease or other relevant contraindications. This is not a complete list, so suitability must be determined by a doctor rather than a BMI result alone.
Some lean tissue loss can occur with any meaningful weight reduction. Adequate protein, regular resistance training, a sustainable rate of loss and clinician-led dose review can support lean-mass retention. Body composition, strength and food intake should be reviewed alongside scale weight.
No. Dose progression should be individualised according to response and tolerability. A higher dose is not automatically the right goal. The clinical priority is a sustainable plan that supports nutrition, activity, muscle preservation and manageable side effects.
Appetite can return and weight regain is common after treatment stops. In the STEP 1 extension, participants regained about two-thirds of their prior loss within a year of stopping semaglutide. This is why maintenance planning, nutrition, resistance training and follow-up are discussed from the beginning.
These are prescription-only medicines. Singapore’s Ministry of Health and Health Sciences Authority advise against buying them from unknown or unregulated online sellers because products may be unregistered, substandard or counterfeit. Treatment should follow a medical assessment and be supplied through regulated channels.
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Your next step
Understand your metabolic baseline, treatment eligibility and a sustainable path forward with an SMC-registered doctor.
Book a consultationHisential Orchard Clinic
333A Orchard Road, #04-13 Mandarin Gallery
Singapore 238897
Weekdays 10am-7pm · Sat-Sun 10am-5pm
Related conditions: Medical Weight Loss in Singapore, Diabetes Care in Singapore, and Cardiac Care & Heart Screening in Singapore.
Medically reviewed by Dr. Julian Ng, MBBS (University of Sydney), MSc Microbiology (NUS), Cert. Men's Health (SMHS)
Last reviewed 1 May 2026 · Next review 1 November 2026