GNH USA

Europe — EMA

Meriofert

GNH USA supplies Meriofert (Luteinising hormone, Follicle‑stimulating hormone), a gonadotropin for infertility due to anovulation, hypogonadotropic

Luteinising Hormone (Human), Follicle-Stimulating Hormone

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What is Luteinising Hormone (Human), Follicle-Stimulating Hormone?

Luteinising hormone (human), Follicle‑stimulating hormone, the active ingredient in Meriofert, is a gonadotropin presented as an injectable preparation for intramuscular or subcutaneous use. It is used to treat infertility related to anovulation, hypogonadotropic hypogonadism, and to support assisted reproductive technologies such as in‑vitro fertilisation. The product contains a combination of human LH and FSH that mimics natural pituitary secretion.

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

What is Luteinising Hormone (Human), Follicle-Stimulating Hormone used for?

Meriofert, a gonadotropin preparation, is indicated for conditions involving impaired ovarian function and hormonal deficiency. - Infertility due to anovulation: stimulates follicular development and induces ovulation. - Hypogonadotropic hypogonadism: replaces deficient LH and FSH to restore normal gonadal function. - Assisted reproductive technology (e.g., in vitro fertilisation): supports controlled ovarian stimulation for oocyte retrieval.

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

Meriofert may be associated with a range of adverse reactions following injection.

Common Side Effects: - Injection site pain: mild to moderate discomfort at the injection site. - Headache: transient headache of varying intensity. - Nausea: occasional nausea without vomiting. - Abdominal discomfort: mild abdominal cramps or bloating. - Ovarian hyperstimulation syndrome (mild): mild symptoms such as abdominal distension.

Serious or Rare Side Effects: - Ovarian hyperstimulation syndrome (severe): marked ovarian enlargement, ascites, thromboembolism. - Thromboembolic events: deep vein thrombosis or pulmonary embolism. - Allergic reaction: rash, urticaria, or anaphylaxis. - Ectopic pregnancy: occurrence of pregnancy outside the uterus. - Multiple pregnancy: higher‑order gestations (triplets or more).

What precautions apply to Luteinising Hormone (Human), Follicle-Stimulating Hormone?

Before using Meriofert, clinicians should consider several precautionary measures to minimise risks. - Patient assessment: evaluate ovarian reserve and baseline hormone levels. - Monitoring: perform regular ultrasound and estradiol monitoring during treatment. - OHSS risk: assess risk factors such as polycystic ovary syndrome and adjust dose accordingly. - Contraindications: avoid use in known hypersensitivity to gonadotropins or active ingredients. - Pregnancy status: discontinue if pregnancy is confirmed before intended ovulation trigger. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Luteinising Hormone (Human), Follicle-Stimulating Hormone interact with?

Meriofert can interact with other medications that affect hormonal balance or coagulation.

Major Interactions (Avoid): - GnRH agonists/antagonists: may alter the intended gonadotropin response. - Anticoagulants: increased risk of bleeding with severe ovarian hyperstimulation. - Aromatase inhibitors: may interfere with estrogen synthesis during stimulation.

Moderate Interactions (Monitor Closely): - Corticosteroids: may affect ovarian response, requiring dose adjustment. - Thyroid hormones: abnormal thyroid status can modify gonadotropin efficacy. - Insulin or oral hypoglycemics: hyperstimulation may affect glucose metabolism.

Frequently asked questions

What is Meriofert used for?+
Meriofert is a gonadotropin preparation indicated for infertility caused by anovulation, for patients with hypogonadotropic hypogonadism, and as part of assisted reproductive technology protocols such as in‑vitro fertilisation to stimulate ovarian follicle development and ovulation.
How does luteinising hormone (human) and follicle‑stimulating hormone work?+
The LH component binds to LH receptors on theca cells, promoting androgen production that is converted to estrogen, while the FSH component activates FSH receptors on granulosa cells, stimulating follicular growth and estrogen synthesis. Together they mimic the natural pituitary signal that leads to final oocyte maturation and ovulation.
What is the usual dose of Meriofert?+
The dose of Meriofert is individualized. A qualified prescriber determines the amount, frequency and duration of treatment based on the patient’s hormonal profile, ovarian response and the specific assisted‑reproduction protocol being used.
Is Meriofert safe during pregnancy or breastfeeding?+
Meriofert is intended for use before conception to achieve pregnancy. It is not recommended for use during an established pregnancy or while breastfeeding, and treatment should be discontinued once pregnancy is confirmed unless a specialist advises otherwise.
How do I order Meriofert from GNH USA?+
To order Meriofert, submit an enquiry on the product page at gnh-usa.com with 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 if required) and the necessary import documentation.
How does Meriofert compare with the main alternative drug or class?+
Meriofert combines both LH and FSH in a single preparation, whereas some alternatives provide only recombinant FSH (e.g., Gonal‑F) or separate LH preparations. The combined formulation can simplify dosing schedules and may better mimic natural pituitary output, but choice depends on individual patient response and clinician preference.
What are the storage and handling requirements for Meriofert?+
Meriofert must be stored at 2‑8 °C (refrigerated), protected from light, and should never be frozen or shaken. Keep the product in its original packaging until use and discard any vial that has been left at room temperature for longer than the time specified in the label.
How is Meriofert administered?+
Meriofert is administered by intramuscular or subcutaneous injection. The vial is reconstituted with the appropriate diluent according to the label, and the dose is injected using a sterile needle and syringe under aseptic technique, following the prescriber’s instructions.
What are the most serious risks to watch for with Meriofert?+
The most serious risks include severe ovarian hyperstimulation syndrome (OHSS) which can lead to ovarian rupture, thromboembolic events, allergic reactions such as anaphylaxis, and the possibility of multiple or ectopic pregnancies. Patients should be monitored closely for these complications.
Who should not use Meriofert?+
Meriofert should not be used in individuals with known hypersensitivity to human LH or FSH, in patients with uncontrolled ovarian cysts, active ovarian or breast cancer, severe uncontrolled endocrine disorders, or in women who are already pregnant.
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
Luteinising Hormone (Human), Follicle-Stimulating Hormone
Route
Intramuscular Use , Subcutaneous Use
Manufacturer
Ibsa Farmaceutici Italia
Origin
EU

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