Product image of Gonal-F (Follitropin Alfa) supplied by GNH India

Gonal-F

Active Ingredient:
Follitropin Alfa
Origin:
EU

Gonal-F (Follitropin Alfa)

Gonal‑F is a prescription medication that contains the recombinant hormone follitropin alfa, supplied as a sterile solution for subcutaneous injection. It belongs to the follicle‑stimulating hormone (FSH) class and is used in reproductive medicine to support ovarian follicle development. Manufactured for the European market, Gonal‑F provides a standardized source of FSH for fertility treatment protocols. It is administered by a healthcare professional and requires individualized dosing based on patient response.

Manufacturer / TM Owner

Merck Europe B.V.

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Indications & Clinical Uses

Gonal‑F is indicated for several fertility‑related conditions where stimulation of the ovaries is required.

  • Treatment of infertility caused by anovulation, such as in polycystic ovary syndrome.
  • Controlled ovarian stimulation in assisted reproductive technology cycles, including in vitro fertilisation (IVF) and intracytoplasmic sperm injection (ICSI).
  • Induction of ovulation for women with hypogonadotropic hypogonadism.
  • Use in combination with other gonadotropins or luteinising hormone preparations as part of a comprehensive fertility protocol.

Side Effects

Side effects reported with Gonal‑F vary in frequency and severity; they are generally related to the drug’s action on ovarian tissue and the hormonal changes it induces.

Common

  • Mild abdominal discomfort or bloating.
  • Local injection site reactions such as redness, swelling, or itching.
  • Headache or mild fatigue.
  • Ovarian hyperstimulation syndrome (OHSS) in its mild form, presenting with abdominal distension and mild nausea.
  • Nausea or mild vomiting.

Serious

  • Severe OHSS, characterized by rapid weight gain, significant abdominal pain, and shortness of breath.
  • Ovarian cyst formation that may require surgical intervention.
  • Allergic reactions including rash, urticaria, or anaphylaxis.
  • Thromboembolic events, though rare, have been observed in patients with severe OHSS.

Precautions & Warnings

When prescribing Gonal‑F, clinicians consider several safety factors to minimise risks and optimise treatment outcomes.

  • Evaluate baseline ovarian reserve and monitor follicular response throughout therapy.
  • Use the lowest effective dose and adjust based on ultrasound and estradiol measurements.
  • Counsel patients about the signs of ovarian hyperstimulation syndrome and advise prompt medical attention if symptoms develop.
  • Avoid use in patients with known hypersensitivity to any component of the formulation.
  • Exercise caution in women with uncontrolled thyroid disease, adrenal insufficiency, or pituitary disorders.
  • Consider postponing treatment in pregnancy or while breastfeeding, as safety has not been established.

Avoid Interactions

Gonal‑F may interact with other medications or substances that affect hormone levels, ovarian response, or fluid balance.

Avoid

  • Concurrent use of high‑dose estrogen‑containing oral contraceptives, which can blunt the ovarian response to FSH.
  • Co‑administration of drugs that significantly increase the risk of thromboembolism in patients predisposed to severe OHSS.

Use with caution

  • Gonadotropin‑releasing hormone (GnRH) agonists or antagonists used in assisted reproduction protocols; dosing may need adjustment.
  • Anticoagulants, because severe OHSS can predispose to clot formation.
  • Diuretics, which may mask early signs of fluid shift associated with OHSS.
  • Thyroid hormone replacement, requiring monitoring of thyroid function during stimulation.

Frequently Asked Questions

Gonal‑F contains recombinant follicle‑stimulating hormone that binds to FSH receptors on ovarian granulosa cells, promoting follicular growth and estrogen production, which facilitates ovulation.

Gonal‑F is used for anovulatory infertility, controlled ovarian stimulation in assisted reproductive technology such as IVF or ICSI, and ovulation induction in women with hypogonadotropic hypogonadism.

Gonal‑F is supplied as a sterile solution for subcutaneous injection, typically given by a healthcare professional according to an individualized dosing schedule.

Common side effects include mild abdominal discomfort, injection‑site reactions, headache, fatigue, mild ovarian hyperstimulation syndrome, and occasional nausea or vomiting.

Serious reactions may involve severe ovarian hyperstimulation syndrome with rapid weight gain, intense abdominal pain, shortness of breath, ovarian cysts requiring surgery, allergic reactions such as rash or anaphylaxis, and rare thromboembolic events.

Gonal‑F is not recommended during pregnancy or while breastfeeding because safety in these conditions has not been established.

Patients are typically monitored with serial transvaginal ultrasounds and serum estradiol measurements to assess follicular development and adjust dosing as needed.

High‑dose estrogen‑containing oral contraceptives and medications that markedly increase thromboembolic risk should be avoided during Gonal‑F therapy.

The product should be stored in a refrigerator (2‑8 °C) and protected from light; it should not be frozen. Once in use, follow the manufacturer’s guidance on stability at room temperature.

Patients should contact their fertility specialist immediately if they experience rapid weight gain, severe abdominal pain, persistent nausea, vomiting, or shortness of breath, as these may signal ovarian hyperstimulation syndrome.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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