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Medical Weight Management  ·  Healthy Aging & Longevity

Tesamorelin

Egrifta (FDA-approved brand), Egrifta SV (FDA-approved brand)

A growth-hormone-releasing hormone (GHRH) analog. FDA-approved only for reducing excess abdominal fat in adults with HIV-associated lipodystrophy; any other use is off-label.

Baseline Labs Required FDA-Approved (Different Indication) Subcutaneous injection (daily) Prescription Consultation Required
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What Is It?

Tesamorelin is a synthetic analog of growth-hormone-releasing hormone (GHRH). By stimulating the pituitary to release growth hormone in a physiologic pattern, it may influence body composition. The FDA-approved tesamorelin product (Egrifta / Egrifta SV) is specifically indicated for the reduction of excess abdominal fat in adults with HIV-associated lipodystrophy. It is not FDA-approved for general weight loss, athletic performance, or anti-aging use. Any other use represents an off-label decision that requires careful provider review.

What May It Support?

  • Body composition (being evaluated in select settings)
  • Reduction of excess abdominal fat in FDA-approved patient population
  • Adjunctive support in a broader provider-directed plan

Which Programs May Include It?

Where It Fits

Binds pituitary GHRH receptors to stimulate endogenous growth hormone release in a pulsatile, physiologic pattern.

Beginner
Not typical
Intermediate
Not typical
Advanced
Provider-directed use

Do I Need Bloodwork?

Baseline Labs Required

Regular follow-up with IGF-1 monitoring and periodic metabolic labs at intervals determined by the provider.

Likely baseline panel may include: CBC, CMP, A1c, Lipid panel, IGF-1, TSH, Pregnancy test when applicable

Important Safety Information

Common side effects may include:

  • Injection-site reactions
  • Joint pain (arthralgia)
  • Muscle pain (myalgia)
  • Fluid retention or peripheral edema
  • Numbness or tingling in the extremities
  • Elevated blood glucose
Serious WarningsMay increase IGF-1; excess IGF-1 signaling has been associated with cancer risk
May cause or worsen glucose intolerance and hyperglycemia
Fluid retention, including carpal tunnel syndrome
Hypersensitivity reactions have been reported

Drug interactions: May interact with corticosteroids, thyroid hormone, insulin, and other medications that affect glucose metabolism. Provider should review the complete medication list before prescribing.

Contraindications:

  • Active malignancy
  • Disruption of the hypothalamic-pituitary axis (e.g., hypophysectomy, hypopituitarism, pituitary tumor or surgery, head irradiation, or head trauma)
  • Pregnancy
  • Known hypersensitivity to tesamorelin or mannitol
Pregnancy & BreastfeedingNot recommended during pregnancy or while breastfeeding. Discuss reproductive plans with your provider before starting.
Cancer-Related ConsiderationsNot for patients with active malignancy. Because tesamorelin can raise IGF-1, any personal or family history of cancer must be discussed with your provider before considering therapy.

Regulatory Status

Tesamorelin (Egrifta / Egrifta SV) is FDA-approved for the reduction of excess abdominal fat in adults with HIV-associated lipodystrophy. It is specifically not indicated for weight-loss management. Any other use is off-label.

Compounded MedicationIf a compounded tesamorelin product is prescribed, please note that compounded medications are not FDA-approved and are not reviewed by FDA for safety, effectiveness, or quality before marketing.

Frequently Asked Questions

Is tesamorelin FDA-approved for weight loss?
No. The FDA-approved tesamorelin product is indicated only for the reduction of excess abdominal fat in adults with HIV-associated lipodystrophy. Use for general weight loss or anti-aging is off-label and requires careful provider review.
Do I need bloodwork before starting?
Yes. Baseline laboratory testing is required because tesamorelin affects the growth-hormone axis and can influence blood sugar and IGF-1 levels.
Can I take tesamorelin if I have a history of cancer?
Tesamorelin is contraindicated in patients with active cancer. Any personal or family cancer history must be disclosed and reviewed by your provider before this therapy is considered.
How long is treatment continued?
Duration is determined by the provider based on response, laboratory findings, and tolerability. Regular follow-up and monitoring are required throughout treatment.

Consultation

Treatment is not automatically provided. A licensed medical provider must review your history, symptoms, medications, laboratory results, and treatment goals before determining eligibility.

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Not Medical Advice

The information provided on this website is for general educational purposes and is not medical advice, a diagnosis, or a prescription. Treatment recommendations are not final until a licensed medical provider completes a live consultation, reviews your medical history and medications, evaluates relevant laboratory results, and determines that treatment is medically appropriate.

Compounded Medication Disclosure

Certain treatments may be prepared by a compounding pharmacy pursuant to an individual prescription. Compounded medications are not FDA-approved, and FDA does not review them for safety, effectiveness, or quality before marketing.

Results

Your results identify subjects to discuss with a provider. They do not establish medical eligibility or guarantee that any medication will be prescribed.

Emergencies

This website is not intended for emergencies. Call 911 or seek immediate medical attention for urgent or severe symptoms.