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Tesamorelin Peptide - Dragon Pharma

Dragon Pharma

Tesamorelin Peptide - Dragon Pharma

Injection · 5 mg · vial

In stock · ships within 24h Out of stock Ships from International · U.S Domestic
CompoundTesamorelin
ClassGHRH analog peptide
Half-life8-38 minutes
DetectionBanned at all times, S2
Liver toxicityLow
Water retentionLow to moderate
A single 5 mg lyophilised vial of a stabilised growth hormone releasing hormone analog. The approved injectable form is used daily for visceral fat in lipodystrophy, and the clinical schedule is long rather than a short cycle. Elimination is measured in minutes, from an average near 8 minutes on the SV label to 26-38 minutes in general reference data, so one 5 mg vial does not cover a week at the approved daily dose.
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Tesamorelin Peptide - Dragon Pharma
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$80.00
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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.

Buy Tesamorelin by Dragon Pharma at Best Anabolic Steroids. The pack holds one lyophilised vial with 5 mg of tesamorelin, a stabilised analogue of growth hormone releasing hormone, so the strength you actually work with depends on how much solvent you add rather than on a fill line. The approved injectable form of this molecule - sold as Egrifta for excess visceral fat in lipodystrophy - is the reason human data exist for it at all; the vial on this page is a research material rather than that pharmaceutical presentation, and this description keeps the two apart throughout.

It is a peptide for a sustained routine, not a short push, and the numbers further down explain why.

Product Overview

What arrives is a single glass vial of lyophilised powder: 5 mg of tesamorelin peptide, sealed, produced under GMP conditions, with the mass of active material stated on the label. It is not a ready-to-inject solution and there is no solvent in the box, so the buyer supplies bacteriostatic water and calculates the concentration from the volume added. A 5 mg vial reconstituted with a stated volume gives a fixed number of doses at a fixed strength, which is why the arithmetic matters more here than the label figure.

Tesamorelin is a GHRH analogue, which puts it in the signalling layer above growth hormone rather than in the hormone itself. The stabilised version is what separates it from older GHRH peptides: the same family, but a different stability profile and a very different evidence base. Its approved clinical use - reduction of visceral adipose tissue in patients with lipodystrophy - is what makes it unusual among research peptides, because that approval required human trials rather than anecdote.

Two limits belong in the same paragraph as the strengths. The approved population is narrow, and transferring those results to healthy trained users is not confirmed by any source behind this page. And one 5 mg vial does not cover a week at the approved 2 mg daily step, which is arithmetic rather than a comment on quality.

Mechanism of Action

The peptide binds the GHRH receptor on pituitary somatotrophs and drives release of the body's own growth hormone in pulses, which in turn lifts hepatic IGF-1. That is the opposite approach to supplying recombinant hormone from outside, the route taken by Dragontropin HGH, and it is also different from secretagogues that act on the ghrelin receptor, such as Ipamorelin and Hexarelin. Same end signal, three different doors.

Exposure time is the practical constraint. General reference data put the elimination half-life between 26 and 38 minutes; the label for the SV presentation reports an average of about 8 minutes after a 1.4 mg subcutaneous dose, and the older WR form is listed near 11 minutes. Nothing in that range supports infrequent administration, so the protocol is daily by necessity.

The clinical endpoint was fat, and specifically visceral fat, measured over long daily programmes rather than weeks. IGF-1 rises within hours of a dose while the fat change accumulates over months, so the two markers move on completely different clocks and only one of them is useful for judging a single injection.

What to Expect from a Tesamorelin Routine

  • Growth hormone and IGF-1 rise within hours of a subcutaneous dose, and the response is read on the IGF-1 axis rather than felt.
  • Visceral fat is the endpoint that moved in clinical work, and it moved over months of daily use, not over a single week.
  • Consistency beats escalation. Because the peptide clears in minutes, timing discipline matters more than pushing the amount up.
  • Supply planning is part of the protocol: a 5 mg vial runs out well inside a week at the approved 2 mg daily step.
  • Class effects are dose related: edema, fluid retention, joint aches and injection site reactions are described for GH peptides generally.
  • Tesamorelin is banned at all times under WADA class S2, where it is named directly, which matters to any tested athlete.

Dosing Steps and What One 5 mg Vial Covers

There is no separate research dosing convention for this compound, so the table keeps approved clinical steps apart from what a single vial can deliver.

Approved step 2 mg subcutaneously once daily in the original Egrifta label
Lower approved step 1.4 mg once daily for the SV presentation, with an average half-life near 8 minutes
Frequency Daily; elimination runs from about 8 minutes to 38 minutes, so a weekly injection is not supported
One 5 mg vial Does not cover a week at 2 mg per day - arithmetic, not a statement about potency
Female No verified protocol for women appears anywhere in the source material behind this page
Administration Subcutaneous; the approved site is the abdomen and the injection point moves with every dose

Readers who want a GHRH signal with far fewer injections look at CJC-1295 DAC, whose release profile is measured in days rather than minutes. Readers whose target is fat mass through a different mechanism altogether look at a GLP-1 material such as Tirze-Pep 5mg, or at the 176-191 fragment in AOD 9604 5mg.

Combining Tesamorelin with Other Peptides

Three arrangements come up in the sources and in the way this class is studied. The pattern in all of them is daily use over a long window rather than a four-week block.

Daily GHRH phase
Tesamorelin 5 mg vial - research material + Bacteriostatic water for reconstitution
Daily injections over weeks to months, mirroring the long clinical programmes rather than a fixed vendor cycle
GHRH plus ghrelin pathway
Different receptors, so the pair is a mechanistic combination; the sources give no fixed combined schedule
Longer-acting GHRH option
Tesamorelin - short release, 8-38 minutes + CJC-1295 DAC - slow release
Both are GHRH analogues, but the release profiles differ so widely that schedules are not interchangeable

One comparison is not a stack and is worth stating plainly: recombinant HGH supplies the hormone itself, while this peptide only asks the pituitary for more of it, and IGF-1 LR3 sits one step further downstream entirely.

Reconstitution Arithmetic and IGF-1 Follow-Up

There is no reset step to plan for this compound. Tesamorelin drives growth hormone release through the pituitary and leaves the gonadal axis untouched, so no SERM protocol exists for it; what has to be planned instead is the vial and the monitoring.

ReconstitutionAdd bacteriostatic water and recalculate concentration from the volume added; a 5 mg vial does not map onto the approved milligram steps by default
Vial coverageOne 5 mg vial does not cover a week at the approved 2 mg daily dose
Recovery stepNot applicable: no gonadal suppression, so no PCT route is documented for this peptide
DiscontinuationNo separate withdrawal protocol for the research format was found in the sources
Intended follow-upIGF-1 plus fasting glucose; clinical programmes tracked metabolic panels rather than how the user felt
Sport contextWADA class S2, banned at all times; the listing names tesamorelin directly

Tesamorelin Side Effects and Management

The profile follows the GH peptide class more than the molecule itself, and most entries respond to dose adjustment.

Injection site reactionsRotate sites and use clean technique; expected with daily subcutaneous injections.
Edema and fluid retentionReduce the dose or slow the escalation; described for the class and dose dependent.
Joint and muscle achesLower the dose or pause; reported across GH secretagogues.
Glucose handlingTrack fasting glucose and tolerance; growth hormone signalling can shift both.
Headache and flushingUsually transient and dose related; reduction is the documented step.
Reconstitution errorsThe most common avoidable problem: measure the solvent, write the resulting concentration on the vial, and work from that.

Storing the Tesamorelin Vial and the Mixed Solution

Keep the lyophilisate cold, dry and in its carton, and give the reconstituted solution the refrigerator rather than the shelf: the sources describe no long room temperature window for a mixed peptide solution. Because the peptide clears in minutes, the bottle is the fragile part of the routine, not the molecule. Add the solvent gently down the wall of the vial instead of shaking it, mark the mixing date on the label, and do not refreeze a thawed or mixed vial. Draw each dose with a fresh needle, wipe the stopper with an alcohol swab before entry, keep the vial away from light and out of the reach of children, and dispose of used vials and sharps as medicinal waste under local rules.

Buying Tesamorelin Online

Because the useful facts about this peptide are short and unglamorous - a real approval, a real population, a half-life measured in minutes and a 5 mg vial that does not last a week - and this page states them instead of promising a transformation. The vial is Dragon Pharma tesamorelin at 5 mg of lyophilised powder. Packaging is lab tested and delivery follows the site's usual international and US terms, and the description tells you what the clinical work actually measured so you can decide whether a daily routine fits.

The information on this page is reference material for research and educational purposes and is not medical advice, a prescription or a treatment recommendation. Tesamorelin is described here as a research peptide; the approved pharmaceutical presentations are named only to explain where the published data come from, and this vial is not that product. Amounts, timings and laboratory figures quoted elsewhere in this catalogue do not transfer to this compound automatically. Handle as a laboratory item, keep it away from children, and follow the law where you live.
What is Dragon Pharma Tesamorelin?
It is a single 5 mg lyophilised vial of tesamorelin, a stabilised growth hormone releasing hormone analog, sold as a research material. The molecule acts on the GHRH receptor in the pituitary and drives release of the body's own growth hormone, which then lifts IGF-1. The approved injectable medicine built on the same molecule is used for visceral fat in lipodystrophy, and that approval is where the human dosing data come from.
Is Tesamorelin the same as Egrifta?
The active molecule is the same, the presentation is not. Egrifta and Egrifta SV are approved pharmaceutical products with labelled doses of 2 mg and 1.4 mg daily and a documented manufacturing chain. The Dragon Pharma item is a research vial, so the approved pharmacokinetic and dosing data describe the medicine rather than this presentation.
How often is Tesamorelin injected, given the short half-life?
Once daily, subcutaneously. General reference data give an elimination half-life of 26 to 38 minutes, the SV label reports an average near 8 minutes after a 1.4 mg dose, and the WR form is listed around 11 minutes. Exposure that short cannot be stretched across a week, and the clinical programmes that produced the visceral fat results were daily and long.
How do you reconstitute a 5 mg Tesamorelin vial?
Add bacteriostatic water to the lyophilised powder and divide the stated 5 mg by the volume you added to get the concentration per unit on the syringe. Keep the lyophilisate cold and the mixed solution refrigerated. One vial does not cover a week at the approved 2 mg daily dose, so plan supply before starting.
Tesamorelin vs Ipamorelin - what is the difference?
They work through different receptors. Tesamorelin is a GHRH analog that binds the GHRH receptor, while Ipamorelin acts on the ghrelin receptor. Tesamorelin carries human trial data for visceral fat in a specific patient group; ipamorelin is shorter acting still and is used as a secretagogue in research settings without an approved indication.
Does Tesamorelin reduce visceral fat?
That is the indication it was approved for. Reductions in visceral adipose tissue were recorded in long daily programmes in patients with lipodystrophy, and the effect builds over months rather than days. The population studied was a clinical one, so the result cannot be assumed to transfer unchanged to healthy trained users.
What are Tesamorelin side effects?
Injection site reactions are the most frequent complaint and follow from daily subcutaneous use. Fluid retention and edema, joint and muscle aches, and headache or flushing are the class effects described for GH peptides, all dose related. Because growth hormone signalling can affect glucose handling, the sources also flag glucose and tolerance monitoring.
Do I need post-cycle therapy after Tesamorelin?
No SERM protocol applies. Tesamorelin acts on the pituitary and leaves the gonadal axis alone, so there is nothing for Nolvadex or Clomid to restart, and the source material holds no withdrawal protocol. IGF-1 and glucose are the markers to watch instead.

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