Product image of Gonasi Set (Human Chorionic Gonadotropin) supplied by GNH India

Gonasi Set

Active Ingredient:
Human Chorionic Gonadotropin
Origin:
EU

Gonasi Set (Human Chorionic Gonadotropin)

Gonasi Set is a prescription injectable solution that contains the active ingredient human chorionic gonadotropin (hCG). It is supplied in a dosage form intended for intramuscular or subcutaneous administration and is marketed in the European Union. As a gonadotropin, Gonasi Set mimics luteinizing hormone activity to support ovulation and the luteal phase in assisted reproductive protocols. It is prescribed for infertility treatments and should be handled according to the instructions.

Manufacturer / TM Owner

Ibsa Farmaceutici Italia

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Indications & Clinical Uses

Gonasi Set is indicated for several fertility‑related purposes in assisted reproductive technology.

  • Induction of ovulation in women with anovulatory or oligo‑ovulatory disorders.
  • Luteal phase support following ovulation induction or assisted conception cycles.
  • Treatment of infertility associated with inadequate endogenous hCG production.
  • Use in combination with gonadotropin‑releasing hormone (GnRH) protocols to trigger final oocyte maturation.
  • Support of spermatogenesis in selected male infertility cases (off‑label in some regions).

Side Effects

Side effects reported with Gonasi Set vary in frequency and severity; they are generally related to the injection site or hormonal activity.

Common

  • Injection‑site pain, redness, or swelling.
  • Mild headache or fatigue.
  • Nausea or mild abdominal discomfort.
  • Temporary ovarian enlargement or cyst formation.
  • Breast tenderness or mild edema.

Serious

  • Ovarian hyperstimulation syndrome (OHSS) with rapid weight gain, ascites, or respiratory distress.
  • Allergic reactions such as rash, itching, or anaphylaxis.
  • Thromboembolic events including deep‑vein thrombosis.
  • Ectopic pregnancy in the setting of assisted conception.

Precautions & Warnings

Before prescribing Gonasi Set, clinicians should evaluate patient history and monitor for conditions that could be worsened by hCG therapy.

  • Confirm absence of active ovarian cysts or severe endometriosis.
  • Assess risk factors for ovarian hyperstimulation syndrome, especially in polycystic ovary syndrome.
  • Review personal or family history of thromboembolic disease.
  • Ensure appropriate timing within the menstrual cycle to avoid premature luteinization.
  • Monitor serum estradiol and hCG levels during treatment.
  • Use caution in patients with uncontrolled thyroid disease due to hCG’s thyrotropic effect.

Avoid Interactions

Gonasi Set may interact with other medications or hormonal agents, influencing efficacy or safety.

Avoid

  • Concurrent use of other gonadotropins or hCG products, which can cause excessive hormonal stimulation.
  • High‑dose estrogen therapy that may mask ovarian response.

Use with caution

  • Anticoagulant or antiplatelet drugs, due to increased risk of thrombosis in OHSS.
  • Thyroid hormone replacement, as hCG can affect thyroid function tests.
  • Assisted reproductive protocols involving GnRH agonists or antagonists, requiring dose adjustments.

Frequently Asked Questions

Gonasi Set contains hCG, which mimics luteinizing hormone and stimulates ovulation and supports the luteal phase by promoting progesterone production.

It is given as an injectable solution either intramuscularly or subcutaneously, typically under the supervision of a fertility specialist.

Gonasi Set is supplied as a sterile liquid for injection; specific strength details are defined by the prescribing information.

Women with anovulatory disorders, those undergoing assisted reproductive technology, and patients requiring luteal phase support may benefit.

Common reactions include injection‑site pain, mild headache, fatigue, nausea, abdominal discomfort, and temporary ovarian enlargement.

Signs include rapid weight gain, abdominal distension, shortness of breath, and fluid accumulation; patients should seek medical attention promptly.

Contraindications include known hypersensitivity to hCG, active ovarian cysts, severe endometriosis, and uncontrolled thyroid disease.

In some regions it is used off‑label to support spermatogenesis, but this use should be evaluated by a specialist.

Serial measurements of serum estradiol, hCG levels, and ultrasound monitoring of ovarian response are commonly performed.

The product should be kept refrigerated according to the label, protected from light, and not frozen.

Concurrent high‑dose estrogen from oral contraceptives may interfere with the intended hormonal effect and is generally avoided.

They should stop the medication immediately and seek emergency medical care, as anaphylaxis can be life‑threatening.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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