GNH USA

Europe — EMA

Meriofert

GNH USA supplies Meriofert (Follicle-Stimulating Hormone and Luteinising Hormone), a gonadotropin for infertility treatment and ovarian stimulation.

Follicle-Stimulating Hormone, Luteinising Hormone

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What is Follicle-Stimulating Hormone, Luteinising Hormone?

Follicle-Stimulating Hormone (FSH) and Luteinising Hormone (LH), the active ingredient in Meriofert, is a gonadotropin presented as a sterile injectable solution for intramuscular or subcutaneous use. It is employed to stimulate follicular development and ovulation in women with infertility. 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 is a gonadotropin used in reproductive medicine to address disorders of ovulation and to support assisted reproductive technologies. - Infertility due to anovulation: promotes follicular growth and estradiol production to enable ovulation. - Controlled ovarian stimulation for assisted reproductive technologies: provides coordinated FSH and LH activity to develop multiple mature follicles. - Induction of ovulation in women undergoing IVF: supports the final maturation of oocytes for retrieval.

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

Adverse reactions may occur with any gonadotropin therapy.

Common Side Effects: - Injection site pain or erythema: mild discomfort at the administration site. - Ovarian hyperstimulation syndrome (mild): abdominal bloating and mild discomfort. - Headache: transient tension‑type headache. - Nausea: mild, self‑limiting gastrointestinal upset.

Serious or Rare Side Effects: - Ovarian hyperstimulation syndrome (severe): rapid weight gain, ascites, or respiratory distress. - Thromboembolic events: rare clot formation requiring urgent medical attention. - Allergic reaction: rash, urticaria, or anaphylaxis. - Ectopic pregnancy: rare occurrence following assisted reproduction.

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

Before initiating therapy, clinicians should evaluate patient suitability and monitor response. - Baseline ovarian assessment: perform ultrasound to estimate follicle count. - Monitor estradiol levels: adjust dosing based on serum concentrations. - Watch for signs of OHSS: educate patients on symptoms requiring prompt care. - Contraindications: avoid in known hypersensitivity to gonadotropins or active ingredients. - Storage: 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 ovarian response or coagulation.

Major Interactions (Avoid): - Anticoagulants (e.g., warfarin): increased risk of bleeding with severe OHSS. - GnRH antagonists used concurrently without proper protocol: may blunt intended ovarian stimulation.

Moderate Interactions (Monitor Closely): - Oral contraceptives: may require a washout period before initiating therapy. - Thyroid hormone replacement: altered metabolism may affect ovarian response. - Corticosteroids: may mask early signs of OHSS. - Dopamine agonists: can affect prolactin levels influencing follicular dynamics.

Frequently asked questions

What is Meriofert used for?+
Meriofert is a prescription injectable that combines follicle‑stimulating hormone (FSH) and luteinising hormone (LH) to treat infertility caused by anovulation, to stimulate multiple follicle development for assisted reproductive technologies, and to induce ovulation in women undergoing in‑vitro fertilisation cycles.
How does Follicle‑Stimulating Hormone and Luteinising Hormone work in Meriofert?+
The FSH component binds to FSH receptors on ovarian granulosa cells, promoting follicular growth and estradiol production. The LH component activates LH receptors on theca cells, supporting androgen synthesis and final follicular maturation, together leading to ovulation when the treatment course is completed.
What is the usual dose of Meriofert?+
The dose of Meriofert is individualized. A qualified prescriber determines the amount, frequency, and duration based on the patient’s ovarian reserve, response to monitoring, and the specific assisted reproduction protocol being used.
Is Meriofert safe to use during pregnancy or breastfeeding?+
Meriofert is intended for use before pregnancy to achieve ovulation. It is not administered during an established pregnancy, and safety in breastfeeding has not been established. Women should discuss family planning and lactation considerations with their healthcare provider.
How do I order Meriofert from GNH USA?+
Enquiries are submitted via the product page at gnh-usa.com where you specify the required quantity. GNH USA 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 necessary import documentation.
How does Meriofert compare with other gonadotropin products?+
Meriofert provides a combined FSH and LH formulation, whereas some alternatives offer FSH alone or separate LH preparations. The combined product can simplify dosing schedules and may better mimic natural ovarian physiology, but the choice depends on individual patient response and clinician preference.
What are the storage and handling requirements for Meriofert?+
Meriofert must be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Before use, allow the vial to reach room temperature for a few minutes, inspect for particulate matter, and use aseptic technique for intramuscular or subcutaneous injection.
How is Meriofert administered?+
Meriofert is given by a qualified healthcare professional via intramuscular or subcutaneous injection, typically in the abdomen or thigh. The injection site is rotated to reduce local irritation, and dosing is adjusted according to serial ultrasound and hormone monitoring.
What are the most serious risks associated with Meriofert?+
The most serious risks include severe ovarian hyperstimulation syndrome (OHSS), which can cause rapid fluid accumulation, thromboembolic events, and rare allergic reactions such as anaphylaxis. Prompt recognition and medical management are essential if these symptoms develop.
Who should not use Meriofert?+
Meriofert is contraindicated in individuals with known hypersensitivity to any of its components, in women with ovarian cysts that could rupture, in patients with uncontrolled thyroid disease, and in those with active malignancy or severe cardiovascular disease where ovarian stimulation is unsafe.
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
Intramuscular Use , Subcutaneous Use
Manufacturer
Ibsa Slovakia S.R.O.
Origin
EU

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