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Tesamorelin 2-10 mg Vials - Generic Peptides Tesamorelin 2-10 mg Vials - Generic Peptides Tesamorelin 2-10 mg Vials - Generic Peptides

Generic Peptides

Tesamorelin 2-10 mg Vials - Generic Peptides

Injection · 2 mg · vial

In stock · ships within 24h Out of stock Ships from International · U.S Domestic
CompoundTesamorelin
ClassGHRH analogue
Half-life8-38 minutes
DetectionWADA S2, prohibited
Liver toxicityLow
Water retentionLow
Three freeze-dried vials of the one GHRH analogue in this range that reached pharmacy shelves, sold as Egrifta for excess visceral fat in lipodystrophy. Its action is measured in minutes, so the approved product is a daily injection, and the clinical amounts of 2 mg and 1.4 mg mean a 5 mg research vial does not cover a full week. Nothing on this page is the approved medicine.
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Tesamorelin 2-10 mg Vials - Generic Peptides
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Quality First

All products are manufactured under strict quality standards and independently tested before release. By purchasing, the buyer agrees to use these products in compliance with all applicable laws.

Product Overview

Tesamorelin is a stabilised analogue of growth hormone releasing hormone, and it is unusual in this catalogue for having a licence. The approved injectable is used for excess visceral fat in patients with lipodystrophy, and that narrow indication is the only population in which the clinical numbers were generated. Generic Peptides offers 2 mg, 5 mg and 10 mg lyophilised vials for laboratory use.

Mechanically it is straightforward. The peptide asks the pituitary for a transient rise in endogenous growth hormone, which lifts IGF-1 as a consequence; it does not introduce hormone from outside. What makes it practical in the clinic is the stabilisation, because unmodified GHRH is destroyed in minutes. Even so, the numbers remain short: the label for the SV form gives an average elimination half-life of about eight minutes once 1.4 mg has been injected under the skin, the WR form about eleven minutes, and general references quote 26 to 38 minutes. That is why the approved schedule is daily rather than weekly, unlike CJC-1295 DAC, a different analogue engineered for a much longer stay in the body.

Two caveats belong up front. The clinical population was people with lipodystrophy, so carrying those findings across to healthy users is an assumption rather than a result. And Sermorelin, the older GHRH fragment, shares the receptor but not the evidence base. In sport the peptide is named directly in class S2 and is prohibited at all times.

Dosage Protocol

The table separates what the licence says from what a research vial can actually deliver. No separate female protocol for this material appears in the sources checked.

Item Figure Basis
Approved Egrifta dose 2 mg daily, subcutaneous Licensed product
Approved Egrifta SV dose 1.4 mg daily, subcutaneous Licensed product
Vial coverage A 5 mg vial falls short of one week Arithmetic at the approved amount
Length in clinic Long term, daily Consultation of the clinical programme
Female No confirmed protocol Nothing found outside the licensed population

Reconstitution arithmetic decides how usable a vial is. One millilitre of bacteriostatic water in the 5 mg vial gives 5 mg per millilitre, where the approved 2 mg amount works out at 0.4 ml, or 40 marks on a U-100 barrel. Two millilitres halves the strength, so 2 mg becomes 0.8 ml. The 2 mg vial at 1 ml gives a single day of the licensed amount, and the 10 mg vial at 2 ml reproduces the middle strength at a lower cost per milligram.

Suggested Protocols

In the clinic this peptide is used alone, every day, for as long as the indication lasts. The combinations below describe how it is read beside other peptides rather than a tested schedule.

Fat-focused reading
Tesamorelin - visceral fat endpoint vs AOD 9604 - lipolysis fragment
One has a clinical endpoint behind it, the other a research idea; they are alternatives to compare, not a stack to run together
Growth hormone shelf
Receptor pairing on one side, the growth factor downstream on the other; neither is part of the licensed protocol

Adjacent reading includes HGH Frag 176-191 and Adipotide on the fat-loss shelf, and Somatropin for supplied growth hormone. The clinic did not cycle this peptide on and off the way bodybuilding protocols cycle steroids, so short blocks are a departure from how the data were generated.

What to Expect

  • Growth hormone and IGF-1 answer within hours. The rise after an injection is prompt, but it fades fast and needs repeating the next day.
  • Visceral fat moves over months. The clinical reduction in deep abdominal fat was recorded with long-term daily use, not with a short block.
  • Nothing accumulates. Half-lives of roughly 8 to 38 minutes depending on the form mean the level is back to baseline quickly.
  • The evidence comes from one population. Adults with lipodystrophy were studied; healthy users are extrapolation.
  • Vial arithmetic is limiting. A 5 mg vial does not stretch to a week at the licensed amount, which is a practical constraint rather than a question of potency.
  • Class reactions still apply. Fluid retention, joint aches and injection site effects are described for growth hormone peptides as a group.
  • Doping status is absolute. Class S2 names the compound directly and applies at all times.

Side Effects and Management

What is reported is mostly local and metabolic rather than dramatic, and the clinical programme monitored glucose because of the growth hormone route.

Injection site reactionsRotate the site, keep the technique clean, use bacteriostatic water. Common with daily shots.
Joint and muscle achesLower the amount or pause. Reported across growth hormone peptides.
Fluid retentionReduce the amount and monitor. A class feature rather than a specific finding.
Glucose tolerance changesTrack blood glucose, since growth hormone and IGF-1 both influence it. The clinic followed metabolic markers.
Headache and flushingSmaller amounts and a settled daily routine usually manage it. Uncommon.

Post-Cycle Therapy (SERM Protocol Not Applicable)

There is nothing to restart. The peptide raises endogenous growth hormone and leaves the gonadal axis alone, so tamoxifen, clomiphene and hCG have no role, and the clinical material contains no withdrawal protocol of that kind.

OnsetNot applicable: no suppression of natural testosterone production
Option ANot applicable
Option BNot applicable
StoppingNo tapering regimen is described for the research format
Follow-upIGF-1 and blood glucose, which is what the clinical programme tracked

Keep the powder refrigerated and dark, and hold the mixed solution in the fridge without freezing it. The consumer shelf life of these specific vials after dilution has not been confirmed.

This material is published for educational and research reference purposes only. The compounds described are research-grade materials supplied for laboratory work and are not presented here as medicines or as a treatment for any condition. Dosing information reflects published clinical and reference data for the active substances, not a recommendation or a prescription. Nothing on this page should be read as medical advice. Keep all products out of reach of children and follow the regulations that apply in your country.
What is tesamorelin and what is it approved for?
A stabilised growth hormone releasing hormone analogue, licensed as Egrifta for excess visceral fat in patients with lipodystrophy. It raises endogenous growth hormone rather than supplying any, and the vials on this page are not that medicine.
How long does tesamorelin last after an injection?
Minutes, not hours. The SV label reports roughly eight minutes of elimination half-life after 1.4 mg subcutaneously, the WR form about eleven minutes, and general references give 26 to 38 minutes. That is the reason for a daily injection.
What amounts are used in the clinical programme?
2 mg daily for the original product and 1.4 mg daily for the SV version, both injected under the skin. Those are licensed amounts for a specific patient group and not a recommendation for research material.
Does a 5 mg vial cover a week?
No. Seven days at 2 mg needs 14 mg of powder, and at 1.4 mg it needs just under 10 mg, so a 5 mg vial supplies only a few days. This is arithmetic, not a statement about potency.
How does tesamorelin differ from sermorelin?
Both are GHRH analogues working at the same receptor, but they are not interchangeable. Tesamorelin is stabilised, has a licensed version and clinical data in lipodystrophy, while sermorelin is the older fragment whose pharmacy product was discontinued.
What does tesamorelin do to visceral fat?
The fall in deep abdominal fat was measured over long-term daily use in the licensed group, which is why the molecule is known for that endpoint. The result belongs to that population and that schedule, not to a short block in healthy users.
Which side effects are reported?
Injection site reactions, joint and muscle aches, fluid retention, headache and flushing, plus changes in glucose handling that require monitoring. The clinical programme followed metabolic markers for exactly that reason.
Is tesamorelin prohibited in sport?
Yes. Growth hormone releasing hormone and its analogues fall under class S2, where tesamorelin is named explicitly, and the prohibition applies at all times including out of competition.

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Tesamorelin 2-10 mg Vials - Generic Peptides
2 mg · International

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