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Gonadorelin Acetate – GnRH Peptide

Gonadorelin Acetate – GnRH Peptide

Price range: د.إ1,125.00 through د.إ4,500.00

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Hypothalamic GnRH peptide used in hormone-axis assessment and targeted reproductive support programs.
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    Performance
  • Hormone support - 9/10
    Hormone support
  • Gonadorelin is a synthetic form of gonadotropin-releasing hormone (GnRH) – the signal the brain sends from the hypothalamus to the pituitary to tell it to release LH and FSH. These pituitary hormones then act on the ovaries or testes to regulate sex hormone production, fertility and aspects of reproductive function. Instead of adding testosterone, oestrogen or other downstream hormones directly, Gonadorelin works right at the top of this axis, briefly stimulating GnRH receptors in the pituitary to create a pulse of LH and FSH, which can then be used diagnostically or, in some programs, as part of an approach to support the body’s own reproductive hormone signalling.

    In conventional medicine, Gonadorelin is used in diagnostic testing (e.g. to assess pituitary function) and, in some cases, to help stimulate ovulation. In advanced wellness and hormone-optimisation settings, it may be used off-label in carefully selected adults as part of programs aimed at supporting endogenous testosterone or oestrogen production, evaluating hypothalamic–pituitary–gonadal (HPG) axis responsiveness, or helping re-establish signalling after suppression (for example, post certain medications or exogenous hormones). It is not a simple libido shot or cosmetic hormone tweak; its primary value lies in how it can test and support the communication between brain, pituitary and gonads under close supervision.

    Because Gonadorelin sits so high in the hormone cascade, it must be used thoughtfully. It’s only appropriate when a clinician has taken a thorough history, ordered the right pathology and decided that acting at the GnRH level is both safe and potentially useful. It is best viewed as a specialist hormone-axis tool within a structured plan, not a general wellness peptide or self-prescribed hormone solution.

  • When used as directed and as part of a specialist-designed plan, Gonadorelin is typically used to help support or assess:

     

    HPG axis function (brain–pituitary–gonadal communication)

    Gonadorelin can help clinicians understand how well the hypothalamus–pituitary–gonadal axis is working by provoking a controlled LH/FSH response.

     

    Endogenous sex hormone production

    In some contexts, short-term or pulsed use may assist in stimulating the body’s own production of testosterone or oestrogen/progesterone via LH and FSH signalling, where appropriate.

     

    Reproductive and fertility pathways

    Under specialist care, Gonadorelin or GnRH analogues may be integrated into protocols to support ovulation or fertility-related assessment and management.

     

    Transition and recovery phases in hormone programs

    In select individuals, Gonadorelin may be considered as part of post-cycle or transition plans to help re-engage the axis, always under endocrinology or experienced prescriber supervision.

     

    *Individual results vary. Gonadorelin is not a replacement for full endocrine management and is not a stand-alone treatment for infertility, hypogonadism or any hormone disorder. It must be integrated into a medically supervised hormone plan.

  • UAE MadeVegan FriendlyGluten FreeCorn Free
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    Ingredient nameDescription
    Gonadorelin acetate100mcg/mL

     

     

    Active Ingredient

    Gonadorelin acetate – 100 mcg/mL

     

    Presentation – Injectable Vial

    Strength: 100 mcg/mL

    Volume: 5 mL multidose vial

    Total peptide content per vial: 100 mcg/mL × 5 mL = 500 mcg per vial

     

    Excipients

    Sterile diluent (e.g., bacteriostatic saline) and standard compounding excipients as specified by the partner pharmacy (may include buffering agents and preservatives).

  • Protocol & Standard Dosing

     

    Low-range test/support dose: e.g. 10–25 mcg per dose

     0.10–0.25 mL per injection

     

    Moderate-range test/support dose: e.g. 25–50 mcg per dose, depending on body size and protocol

     0.25–0.50 mL per injection

     

    Frequency patterns will depend entirely on the purpose:

    • For axis assessment / stimulation testing:
      Often a single dose given at a specific time, followed by timed blood draws for LH/FSH and possibly sex steroids.
    • For supportive / pulsed use in optimisation programs (off-label):
      May be used on a short-term, intermittent schedule (e.g. a few times per week, or in specific cycle phases), always defined by the prescriber.

     

    Administration Instructions

    Route: Subcutaneous injection (SC) into fatty tissue (e.g. lower abdomen or outer thigh), unless your prescriber specifies IV use in a diagnostic setting.

     

    Technique:

    Clean skin, pinch a fold of fat, inject as shown by your nurse or clinician, rotate injection sites and dispose of sharps safely.

     

    Timing:

    For diagnostic testing, timing is tightly linked to blood test timing.

    Dosing is highly individual and depends on whether Gonadorelin is being used diagnostically or as part of a hormone-support program. Your prescribing clinician will specify exact dose (mcg), volume (mL) and schedule on your prescription and nursing instructions.

     

     

    Side Effects, Reactions & Medical Contraindications

     

    Use is generally not recommended in:

    • Known allergy or hypersensitivity to Gonadorelin, GnRH analogues or any component of the vial.
    • Pregnancy or breastfeeding, unless under specialist reproductive/endocrine care for a very specific indication.
    • Known hormone-sensitive tumours (e.g. certain breast, ovarian, uterine or prostate cancers) unless under direct oncology/endocrinology supervision.
    • Uncontrolled pituitary pathology or known pituitary tumours without endocrinologist involvement.
    • Severe, unstable systemic illness where hormone-provocation testing would be unsafe.
    • A detailed endocrine, reproductive and oncological history plus appropriate pathology/imaging should be reviewed before Gonadorelin is used.

     

    Common Side Effects and Adverse Reactions

    • Most reported side effects with Gonadorelin are mild and often short-lived, especially when used for single diagnostic doses. These can include:
    • Flushing or warmth, transient headache or light-headedness around the time of injection.
    • Mild nausea or abdominal discomfort in some individuals.
    • Local injection-site reactions such as redness, itching or small bruises.
    • In therapeutic or repeated-use settings, hormonal fluctuation symptoms may appear (e.g. temporary changes in mood, libido, breast tenderness, cycle timing or testicular sensation) depending on underlying physiology and treatment goals. Any persistent, uncomfortable or worrying symptoms should be discussed with the prescribing clinician.

     

    Reactions Requiring Medical Attention – Stop injections and seek medical help (or emergency care if severe) if there are:

    • Signs of a serious allergic reaction – widespread rash, hives, swelling of face/lips/tongue or difficulty breathing or swallowing.
    • Severe or persistent headache, visual disturbance, chest pain, marked shortness of breath or palpitations.
    • Any sudden, significant change in menstrual bleeding, pelvic pain, testicular pain or other reproductive symptoms that feels serious or out of character.
    • Any new or rapidly worsening symptom that feels serious, unusual or concerning.

     

    Safety Note

    • Gonadorelin is a core hypothalamic hormone analogue and should never be treated like a generic wellness supplement. It directly interacts with the HPG axis, which regulates fertility, sex hormones and aspects of long-term health. For that reason:
    • It must only be used under qualified medical supervision, ideally involving an endocrinologist or experienced hormone clinician.
    • It should be part of a clear diagnostic or therapeutic plan, with pre- and post-treatment testing where appropriate.
    • It should always be framed as one tool in the broader work of managing endocrine and reproductive health, not a quick fix for libido, fertility or energy.
    • Informed consent is essential so clients understand why it is being used, how long for, what will be monitored and what alternatives exist.
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