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Tesamorelin (10mg)

Table of Contents

Tesamorelin (10mg)

Quickstart Highlights

Tesamorelin (a GHRH analog) is administered as a once-daily subcutaneous injection. Two clinically referenced daily regimens appear in the literature and labeling history.

Dosing & Reconstitution Guide

Educational guide for reconstitution and dosing protocol

Standard / Gradual Approach — Label‑Based (3 mL = ≈3.33 mg/mL)

WEEK DAILY DOSAGE UNITS (mL) PER INJECTION
Weeks 1–12 1.4 mg (1400 mcg) once daily (7×/week) 42 units (0.42 mL)
Weeks 13–16 (Optional) 1.4 mg once daily (7×/week) 42 units (0.42 mL)

Reconstitute a 10 mg vial with 3.0 mL to yield ≈3.33 mg/mL. Each 1.4 mg dose equals ~0.42 mL (42 units) on a 100‑unit insulin syringe.

Advanced / Aggressive Approach — Legacy Trials (3 mL = ≈3.33 mg/mL)

WEEK RANGE DAILY DOSAGE (MG) UNITS (PER INJECTION)
Weeks 1–12 2 mg (2000 mcg) once daily (7×/week) 60 units (0.60 mL)
Weeks 13–16 (Optional) 2 mg once daily (7×/week) 60 units (0.60 mL)

With 3.0 mL reconstitution (≈3.33 mg/mL), each 2 mg dose equals ~0.60 mL (60 units) — well within a standard 1 mL insulin syringe and comfortably above the ~10‑unit minimum guideline.

Note: Two evidence‑based daily regimens are described: 1.4 mg once daily (current label) and 2 mg once daily (legacy trials). Select one; do not combine. This educational guide is not medical advice.

Protocol Overview

Evidence supports once‑daily subcutaneous dosing of tesamorelin for ≥8–12 weeks.

Dosing Protocol

Choose one daily regimen and remain consistent.

Storage Instructions

Follow formulation‑specific instructions; do not refrigerate reconstituted tesamorelin.

Suppilies Needed

Estimate vials based on your chosen regimen and cycle length (daily injections, 7×/week).

Important Notes

Key considerations when working with tesamorelin.

How This Works

Tesamorelin is a synthetic analog of growth hormone–releasing hormone (GHRH) that binds pituitary GHRH receptors, increasing pulsatile GH secretion and raising IGF‑1. Clinical studies demonstrated reductions in visceral adipose tissue and favorable effects on certain metabolic markers in indicated populations.

Potential Benefits & Side Effects

Observed in clinical research; individual responses vary.

Lifestyle Factors

Support favorable outcomes with fundamentals:

Injection Technique

General subcutaneous administration considerations.

Recommended Source

We recommend Go Alpha Labs  for high‑purity Tesamorelin (10 mg).

 

Why Go Alpha Labs?​

 Important Note:

This guide is for educational and research use only. It does not provide medical advice or directions for patient care. Always follow applicable regulations and consult qualified professionals.

 

 
 

References:

 

Source Link
EGRIFTA WR™ Prescribing Information (2025) – multi-dose with BAC; one reconstituted vial provides daily doses for 7 consecutive days; room-temperature storage (no refrigeration) View Source
EGRIFTA SV® Prescribing Information – daily 1.4 mg; reconstitute and use immediately; do not refrigerate reconstituted solution View Source
EGRIFTA SV® HCP — Reconstitution – “Once reconstituted, administer immediately” View Source
EGRIFTA SV® HCP — Storage – non-reconstituted vials stored at room temperature; keep out of light View Source
Drugs.com — Tesamorelin / EGRIFTA WR – patient storage note: discard unused after 7 days; room-temperature storage View Source
EMPR (2025) – new WR formulation approved; WR and SV not substitutable; room-temperature storage after reconstitution View Source
Falutz et al., N Engl J Med (2007) – randomized trial showing VAT reduction with daily tesamorelin (2 mg) View Source
Stanley et al., JAMA (2014) – effects on visceral and hepatic fat metrics over 6 months View Source
JCEM (2010) – pooled/extension analyses of efficacy and safety View Source
Fourman et al., Metab & Inflammation (2017) – VAT reduction associations; open-access review View Source
FDA Original Label (2010) – immediate use after mixing; do not refrigerate reconstituted solution View Source
Sigma-Aldrich – general peptide handling & storage guidance for research use View Source
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