GNH USA

Europe — EMA

Meriofert

GNH USA supplies Meriofert (Follicle-Stimulating Hormone; Luteinising Hormone), a gonadotropin for infertility due to anovulation, hypogonadotropic

Follicle-Stimulating Hormone, Luteinising Hormone

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What is Follicle-Stimulating Hormone, Luteinising Hormone?

Follicle-Stimulating Hormone; Luteinising Hormone, the active ingredient in Meriofert, is a gonadotropin presented as an injectable solution for subcutaneous use. It is used to stimulate ovarian follicular development in women with infertility related to anovulation or hypogonadotropic hypogonadism.

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

What is Follicle-Stimulating Hormone, Luteinising Hormone used for?

Meriofert acts on the reproductive hormone axis to support follicular growth and ovulation in several infertility contexts.

Infertility due to anovulation: induces ovulation by stimulating follicle development. Hypogonadotropic hypogonadism: replaces deficient gonadotropins to restore ovarian function. Assisted reproductive technology (ART) protocols: provides controlled ovarian stimulation for egg retrieval.

What are the side effects of Follicle-Stimulating Hormone, Luteinising Hormone?

Meriofert may cause a range of adverse reactions, from mild to severe. Monitoring and prompt reporting are essential.

Common Side Effects: - Injection site pain or erythema. - Mild abdominal discomfort or bloating. - Nausea or mild headache. - Transient mild ovarian hyperstimulation syndrome. - Mood changes or fatigue.

Serious or Rare Side Effects: - Severe ovarian hyperstimulation syndrome with rapid weight gain and fluid accumulation. - Allergic reactions including anaphylaxis. - Thromboembolic events such as deep vein thrombosis. - Multiple pregnancy resulting from excessive follicular response. - Ectopic pregnancy.

What precautions apply to Follicle-Stimulating Hormone, Luteinising Hormone?

Prior to initiating Meriofert, clinicians should assess patient suitability and monitor response closely.

Monitor ovarian response: use serial ultrasound and estradiol measurements. Assess contraindications: avoid in active ovarian cysts or uncontrolled thyroid disease. Avoid use in pregnancy: the drug is not indicated for pregnant women. Consider risk of multiple pregnancy: limit the number of developing follicles. Adjust dose in renal or hepatic impairment: follow prescriber guidance. Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Follicle-Stimulating Hormone, Luteinising Hormone interact with?

Meriofert may interact with other medications that influence hormonal balance or coagulation.

Major Interactions (Avoid): - GnRH agonists: can amplify response and increase risk of severe ovarian hyperstimulation. - Estrogen‑containing contraceptives: may antagonize the intended ovulatory effect. - High‑dose corticosteroids: may alter hormone metabolism and reduce efficacy.

Moderate Interactions (Monitor Closely): - Anticoagulants: monitor for bleeding if ovarian cyst rupture occurs. - Thyroid hormone therapy: may affect overall hormonal response. - Concurrent use of other gonadotropins: avoid overlapping therapy to prevent excessive stimulation.

Frequently asked questions

What is Meriofert used for?+
Meriofert is a prescription injectable that contains both follicle‑stimulating hormone (FSH) and luteinising hormone (LH). It is used to stimulate ovarian follicle development and induce ovulation in women with infertility caused by anovulation, hypogonadotropic hypogonadism, or as part of assisted reproductive technology (ART) protocols.
How does Follicle‑Stimulating Hormone and Luteinising Hormone work in Meriofert?+
The FSH component binds to FSH receptors on granulosa cells, promoting follicular growth and estradiol production. The LH component binds to LH receptors on theca and luteal cells, supporting the final maturation of the dominant follicle and triggering ovulation. Together they mimic the natural hormonal surge required for successful egg release.
What determines the dose of Meriofert?+
The dose of Meriofert is individualized by the prescribing clinician based on the patient’s age, weight, underlying diagnosis, and response to prior stimulation. Dosage regimens are adjusted using serial ultrasound and hormone monitoring, and the prescriber sets the exact amount and schedule for each treatment cycle.
Is Meriofert safe to use during pregnancy or while breastfeeding?+
Meriofert is not intended for use in women who are already pregnant, and it should be discontinued once pregnancy is confirmed. Safety data for breastfeeding are limited, and the drug is generally avoided during lactation unless the benefits clearly outweigh potential risks, as determined by a qualified healthcare professional.
How do I order Meriofert from GNH USA?+
To place an order, submit an enquiry on the Meriofert product page at gnh-usa.com, specifying the required quantity. GNH USA works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain logistics if needed), and any required import documentation.
How does Meriofert compare with other gonadotropin products?+
Meriofert combines both FSH and LH in a single formulation, which can simplify treatment protocols compared with using separate FSH‑only and LH‑only preparations. This dual‑action approach may reduce the number of injections and improve patient compliance, while delivering comparable efficacy to other recombinant gonadotropin products when used under specialist supervision.
What are the storage and handling requirements for Meriofert?+
Meriofert must be stored refrigerated at 2‑8 °C. Keep the vial in its original packaging, protect it from light, and avoid freezing or shaking the solution. If the product must be transported, use validated cold‑chain containers to maintain the required temperature range throughout delivery.
How is Meriofert administered?+
Meriofert is administered by subcutaneous injection, typically into the abdominal wall or thigh. The injection is performed using a sterile needle and syringe, following aseptic technique. The exact injection site, volume, and timing are determined by the treating physician based on the individual stimulation protocol.
What are the most serious risks associated with Meriofert?+
The most serious risks include severe ovarian hyperstimulation syndrome (OHSS), which can cause rapid weight gain, abdominal pain, and fluid accumulation; allergic reactions ranging from rash to anaphylaxis; thromboembolic events; and the possibility of multiple pregnancy. Patients should be monitored closely for early signs of these complications.
Who should not use Meriofert?+
Meriofert is contraindicated in women with known hypersensitivity to any component of the product, active ovarian cysts, uncontrolled thyroid disease, or those who are already pregnant. It should also be used with caution in patients with severe renal or hepatic impairment, and it is not recommended for individuals with a history of thromboembolic disorders unless specifically advised by a specialist.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Follicle-Stimulating Hormone, Luteinising Hormone
Route
Subcutaneous Use
Manufacturer
Ibsa Farmaceutici Italia
Origin
EU

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