Tesamorelin Peptide Screening Form Template

Tesamorelin is a growth hormone-releasing hormone (GHRH) analogue approved by the FDA for HIV-associated lipodystrophy and used off-label for visceral fat reduction, body composition improvement, and metabolic health. It stimulates pituitary GH release in a physiologic, pulsatile manner. This screening form documents body composition symptoms and screens for metabolic, endocrine, and oncologic contraindications before initiating tesamorelin therapy.

4 sections
17 fields
HIPAA-ready
3 citations

Free Template

Tesamorelin Peptide Screening Form

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Your Practice Name

Tesamorelin Peptide Screening Form

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1

General Patient Information

Please provide your personal information.

First Name

Jane

Last Name

Smith

Date of Birth

Can you confirm you are 18 years or older?

Height

e.g. 5'8"

Weight

e.g. 170 lbs

2

Medical History

Please answer all questions as accurately as possible. Your provider will review this information.

Are you actively taking any medications? If so, please list them.

List all current medications, dosages, and frequencies

Do you have any medication allergies? If so, please list them.

List all known drug allergies and reactions

Are you currently being treated or have you been treated for any medical conditions? If so, please list them.

List all current and past medical conditions

Have you had any past surgeries? If so, please list them.

List all surgeries and approximate dates

What is/was your sex assigned at birth?

Male

Emergency contact name and phone number

Name — (555) 000-0000

Mailing address

123 Main St, City, State, ZIP

Any other questions or concerns?

Optional — share anything else you'd like your provider to know

3

Symptoms

Select all symptoms that currently apply to you.

Which of the following symptoms are you experiencing?
4

Medical Conditions

Select all conditions that currently apply to you.

Do any of the following apply to you?

Preview only. Your live form will include your branding and e-signature capture.

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Compliance & Regulatory Notes

Review these notes before deploying this form in your practice.

Tesamorelin is FDA-approved for HIV-associated lipodystrophy. Off-label use for body composition requires documented informed consent. See FSMB: https://www.fsmb.org

Tesamorelin may increase insulin resistance and blood glucose. Monitor HbA1c and fasting glucose in patients with metabolic disorders.

Active malignancy is a contraindication due to the mitogenic properties of growth hormone. Patients with cancer history require specialist evaluation.

Tesamorelin must be dispensed by a licensed compounding pharmacy for off-label use. See FDA: https://www.fda.gov/drugs/human-drug-compounding

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Sources & References

  1. FDA - Egrifta (Tesamorelin) Prescribing Information
  2. FSMB Off-Label Prescribing Guidelines
  3. Endocrine Society Clinical Practice Guidelines

Frequently Asked Questions

Is Tesamorelin FDA-approved?

Tesamorelin (Egrifta) is FDA-approved for the reduction of excess abdominal fat in HIV-infected patients with lipodystrophy. Off-label use for general body composition requires additional informed consent disclosures.

How does Tesamorelin differ from direct growth hormone injections?

Tesamorelin stimulates the pituitary to release GH in a natural, pulsatile pattern, avoiding the supraphysiologic levels associated with direct GH administration. This generally results in a more favorable side effect profile.