Who may be considered
Eligibility depends on current FDA labeling, BMI, weight-related conditions, prior treatment, medications and risks. A prescriber must confirm that benefits outweigh risks and that the product and indication are appropriate.
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Semaglutide is a GLP-1 receptor agonist. FDA-approved Wegovy products are indicated for chronic weight management in eligible patients alongside reduced-calorie nutrition and increased physical activity, with additional labeled cardiovascular and liver-related indications depending on the current product labeling.
Eligibility depends on current FDA labeling, BMI, weight-related conditions, prior treatment, medications and risks. A prescriber must confirm that benefits outweigh risks and that the product and indication are appropriate.
Semaglutide is contraindicated with a personal or family history of medullary thyroid carcinoma or MEN 2 and with serious hypersensitivity to semaglutide. Pregnancy, pancreatitis history, severe gastrointestinal disease, gallbladder disease, diabetic retinopathy and interacting diabetes medicines require careful review.
These are practical planning ranges, not promises. Your consultation determines the exact plan.
The clinician reviews weight history, health conditions, medications, pregnancy plans and prior attempts, and orders appropriate labs.
If eligible, an FDA-approved product is prescribed when accessible and clinically appropriate. Dose escalation follows product labeling and tolerability.
Nutrition, activity, adverse effects and objective outcomes are monitored. Treatment is changed or stopped when risks, intolerance or lack of benefit outweigh benefit.
Common effects include nausea, vomiting, diarrhea, constipation and abdominal pain. Important risks include pancreatitis, gallbladder disease, dehydration-related kidney injury, severe gastrointestinal reactions, allergic reaction and low blood sugar with certain diabetes drugs. Current labeling includes a boxed warning related to thyroid C-cell tumors.
Prescribing is only one part of safe obesity care. Experienced medical oversight verifies the product source, screens contraindications, manages titration and side effects, preserves lean mass and monitors when treatment should change.
Consultations and follow-up may be in-office or by telehealth for patients physically located in Texas, North Carolina or South Carolina, subject to eligibility and law. Labs or in-person assessment may be required.
Pricing: Consultation required. Medication price varies by FDA-approved product, insurance coverage, pharmacy and dose. Identity Aesthetics does not promise coverage or a fixed medication cost.
When a prescription or compounded preparation is clinically appropriate, the dispensing pharmacy, facility classification and current license status matter. Compounded medications are not FDA-approved drug products.
Medical-content evidence review: September 3, 2026. Content is written for patient education and structured from current primary regulatory, labeling and professional sources. It has not been individualized to your medical history. Product labeling and guidance can change; a licensed Identity Aesthetics provider confirms current suitability, informed consent and treatment details before care.
Bring your goals, questions, medication list and prior treatment history. We will help you decide whether Semaglutide for Medical Weight Management—or an alternative—makes sense.
Explore connected treatment guidance, meet the clinical team or begin a personalized consultation.
Patient education developed from primary regulatory, labeling and professional sources.
Physician review across metabolic, hormone and weight-management care.
