GNH USA

Europe — EMA

Methofill

GNH USA supplies Methofill (Methotrexate), a disease-modifying antirheumatic drug for rheumatoid arthritis, psoriasis and certain cancers.

Methotrexate

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What is Methotrexate?

Methotrexate, the active ingredient in Methofill, is a Antimetabolite (Folate antagonist) presented as a subcutaneous injection for Subcutaneous use. It is used to manage rheumatoid arthritis, severe psoriasis, certain leukemias and lymphomas, and ectopic pregnancy.

GNH USA supplies Methofill as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

What is Methotrexate used for?

Methofill (methotrexate) acts as a folate antagonist to modify disease processes in several immune‑mediated and malignant conditions. - Rheumatoid arthritis: reduces joint inflammation and slows disease progression. - Psoriasis: decreases skin cell proliferation and improves plaque lesions. - Acute lymphoblastic leukemia: interferes with malignant cell replication to achieve remission. - Non‑Hodgkin lymphoma: impedes tumor growth and induces cancer cell death. - Ectopic pregnancy: halts trophoblastic tissue development to allow medical resolution.

What are the side effects of Methotrexate?

Methofill may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects: - Nausea or vomiting. - Fatigue or malaise. - Oral mucosal ulceration (mouth sores). - Transient elevation of liver enzymes. - Decreased white blood cell count. - Alopecia (hair thinning).

Serious or Rare Side Effects: - Severe hepatic toxicity or fibrosis. - Pulmonary fibrosis or interstitial pneumonitis. - Life‑threatening bone marrow suppression. - Acute renal failure. - Severe infection due to immunosuppression. - Anaphylactic or severe hypersensitivity reactions.

What precautions apply to Methotrexate?

Methofill requires careful monitoring and specific safety measures before and during therapy. - Pregnancy: contraindicated; teratogenic risk requires effective contraception. - Liver function: monitor transaminases regularly; avoid in severe hepatic disease. - Hematology: perform complete blood counts frequently; discontinue if severe cytopenia occurs. - Renal function: adjust or avoid in significant renal impairment. - Infection: postpone dosing during active infections and avoid live vaccines. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Methotrexate interact with?

Methofill can interact with several medicines, altering efficacy or toxicity.

Major Interactions (Avoid): - Non‑steroidal anti‑inflammatory drugs (NSAIDs): increase risk of renal toxicity and myelosuppression. - Penicillins and other bactericidal antibiotics: may potentiate bone‑marrow suppression. - Live vaccines: heightened risk of severe infection.

Moderate Interactions (Monitor Closely): - Proton‑pump inhibitors: may affect renal clearance. - Diuretics: can exacerbate nephrotoxicity. - Oral contraceptives: reduced effectiveness; supplemental contraception advised. - Other folate antagonists (e.g., trimethoprim): additive hematologic toxicity.

Frequently asked questions

What conditions is Methofill used to treat?+
Methofill contains methotrexate, which is prescribed for rheumatoid arthritis, severe plaque psoriasis, acute lymphoblastic leukemia, non‑Hodgkin lymphoma, and medically managed ectopic pregnancy. In each case the drug works by interfering with cell proliferation or immune activity to control disease symptoms and progression.
How does methotrexate work in the body?+
Methotrexate blocks the enzyme dihydrofolate reductase, stopping the formation of tetrahydrofolate needed for DNA, RNA and protein synthesis. This inhibition particularly affects rapidly dividing cells, such as immune cells and malignant cells, thereby reducing inflammation in autoimmune diseases and limiting tumor growth.
What is the usual dose of Methofill?+
The dose of Methofill is individualized by the prescribing clinician based on the specific indication, patient weight, renal function and treatment response. Only a qualified healthcare professional should determine the appropriate dosing schedule and any necessary adjustments.
Is Methofill safe to use during pregnancy or breastfeeding?+
Methofill is classified as Pregnancy Category X because it is known to cause fetal harm and birth defects. It should not be used by pregnant women, and effective contraception is required for both men and women of child‑bearing potential. Breastfeeding is also contraindicated, as methotrexate can be excreted in milk.
How do I order Methofill from GNH USA?+
To request Methofill, submit an enquiry on the 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 Methofill compare with other treatments for rheumatoid arthritis?+
Methofill (methotrexate) is a conventional synthetic DMARD and is often the first‑line therapy for rheumatoid arthritis due to its proven efficacy and cost‑effectiveness. Biologic DMARDs such as etanercept or adalimumab target specific cytokines and may be used when methotrexate alone is insufficient, but they are generally more expensive and require injection or infusion.
What are the recommended storage conditions for Methofill?+
Methofill should be stored refrigerated at 2‑8 °C. Keep the product in its original packaging, protect it from light, and do not freeze or shake the vial. If temporary temperature excursions occur, consult the supplier before use.
How is Methofill administered?+
Methofill is supplied for subcutaneous injection. A healthcare professional prepares the dose using a sterile syringe and injects it into the subcutaneous tissue, typically in the abdomen or thigh, following aseptic technique. Patients should be trained on proper injection sites and rotation to minimize local reactions.
What are the most serious risks associated with Methofill?+
The most serious adverse events include severe liver toxicity, pulmonary fibrosis or interstitial pneumonitis, profound bone‑marrow suppression leading to pancytopenia, and life‑threatening infections. Early detection through regular laboratory monitoring and prompt reporting of respiratory or hepatic symptoms are essential to mitigate these risks.
Who should not use Methofill?+
Methofill is contraindicated in pregnant or breastfeeding individuals, patients with severe hepatic or renal impairment, those with active infections, and individuals with known hypersensitivity to methotrexate or any component of the formulation. Caution is also advised for patients with pre‑existing lung disease.
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
Methotrexate
Route
Subcutaneous Use
Manufacturer
Accord Healthcare Polska Sp. Z O.O.
Origin
EU

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