Product image of Meriofert (Follicle-Stimulating Hormone, Luteinising Hormone) supplied by GNH India

Meriofert

Active Ingredient:
Follicle-Stimulating Hormone, Luteinising Hormone
Origin:
EU

Meriofert (Follicle-Stimulating Hormone, Luteinising Hormone)

Follicle-Stimulating Hormone, Luteinising Hormone, the active ingredient in Meriofert, is a gonadotropin presented as an injectable solution for intramuscular or subcutaneous use. It is employed to stimulate ovarian follicular development, ovulation and luteal function in patients with reproductive hormone deficiencies.

GNH India supplies Meriofert as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Ibsa Farmaceutici Italia

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Indications & Clinical Uses

Meriofert is a gonadotropin used in reproductive medicine to address disorders of follicular development and ovulation.

  • Infertility due to anovulation: promotes follicular growth and induces ovulation.
  • Assisted reproductive technology (ART): supports controlled ovarian stimulation for IVF cycles.
  • Hypogonadotropic hypogonadism: replaces deficient endogenous FSH and LH to restore normal gonadal function.

How It Works

  • Meriofert contains recombinant Follicle‑Stimulating Hormone and Luteinising Hormone that bind to their respective receptors on ovarian granulosa and theca cells. Activation of FSH receptors stimulates follicular maturation, while LH receptor activation triggers ovulation and luteal phase support, thereby facilitating normal reproductive cycling.

Side Effects

Adverse reactions may occur with any injectable gonadotropin therapy.

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Headache: transient, often resolves without intervention.
  • Nausea: occasional, usually mild.
  • Abdominal bloating: temporary abdominal distension.
  • Mood changes: mild emotional fluctuations.

Serious or Rare Side Effects

  • Ovarian hyperstimulation syndrome (OHSS): potentially severe fluid shift and organ involvement.
  • Thromboembolic events: rare clot formation in veins.
  • Allergic reaction: rash, urticaria, or anaphylaxis.
  • Ectopic pregnancy: rare occurrence during assisted reproduction.
  • Multiple pregnancy: increased risk of twins or higher-order gestations.

Precautions & Warnings

Meriofert should be used under specialist supervision with attention to patient‑specific risk factors.

  • Pregnancy testing: confirm non‑pregnant status before initiating therapy.
  • OHSS monitoring: assess for signs of ovarian hyperstimulation during treatment.
  • Thrombotic risk: evaluate personal or family history of clotting disorders.
  • Allergic history: screen for hypersensitivity to any component of the formulation.
  • Storage: Store at 2‑8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Potential drug interactions may modify the efficacy or safety of Meriofert.

Major Interactions (Avoid)

  • GnRH antagonists: may blunt the intended gonadotropin response.
  • High‑dose estrogen therapy: can suppress endogenous gonadotropin activity.

Moderate Interactions (Monitor Closely)

  • Anticoagulants: monitor for increased bleeding risk if OHSS occurs.
  • Corticosteroids: may affect fluid balance during ovarian stimulation.
  • Thyroid hormones: adjust dosing if thyroid dysfunction is present.

Frequently Asked Questions

Meriofert is an injectable gonadotropin containing Follicle‑Stimulating Hormone and Luteinising Hormone. It is used to treat infertility caused by anovulation, to support ovarian stimulation in assisted reproductive technology cycles, and to replace deficient hormones in hypogonadotropic hypogonadism.

The FSH component binds to receptors on ovarian granulosa cells, promoting follicular growth, while the LH component activates receptors on theca cells and the mature follicle, triggering ovulation and luteal phase support. Together they restore normal ovarian function.

The dose of Meriofert is individualized. A qualified prescriber determines the amount, frequency and duration based on the patient’s clinical condition, response to therapy and treatment protocol.

Meriofert is intended for use before conception to achieve pregnancy. It is not recommended for use during an established pregnancy or while breastfeeding, as safety data in these populations are limited.

Enquiries for Meriofert can be submitted on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain where required) and import documentation.

Meriofert combines both FSH and LH in a single formulation, which can simplify dosing compared with separate FSH‑only or LH‑only preparations. Clinical efficacy is comparable when used according to established reproductive protocols, while the combined product may reduce the number of injections required.

Meriofert must be stored refrigerated at 2‑8 °C. Keep the vials in the original packaging, protect them from light, and avoid freezing or shaking the product to maintain stability.

Meriofert is administered by a healthcare professional via intramuscular or subcutaneous injection, following the dosing schedule prescribed by the treating physician.

The most serious risks include ovarian hyperstimulation syndrome (OHSS), which can be severe and require medical intervention, and rare allergic reactions such as anaphylaxis. Patients should be monitored closely for these events.

Meriofert should not be used in individuals with known hypersensitivity to any component of the product, in patients with active ovarian cysts, uncontrolled thyroid disease, or those at high risk for thromboembolic events without appropriate medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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