GNH USA

Europe — EMA

Methofill

GNH USA supplies Methofill (Methotrexate), an antimetabolite for rheumatoid arthritis, psoriasis, cancers and ectopic pregnancy. Request a quote for supply.

Methotrexate

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What is Methotrexate?

Methotrexate, the active ingredient in Methofill, is an antimetabolite presented as a subcutaneous injection for subcutaneous use. It is used to treat rheumatoid arthritis, severe psoriasis, certain cancers such as leukemia and lymphoma, 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, an antimetabolite, is employed across several disease families where rapid cell proliferation or immune activation is a problem. - Rheumatoid arthritis: reduces joint inflammation and slows disease progression. - Psoriasis: improves skin lesions and decreases plaque formation. - Certain cancers (e.g., leukemia, lymphoma): interferes with malignant cell proliferation. - Ectopic pregnancy: terminates trophoblastic tissue to resolve the pregnancy.

What are the side effects of Methotrexate?

Methofill may cause a range of adverse reactions, from mild to severe.

Common Side Effects: - Nausea and vomiting. - Fatigue or general weakness. - Oral mucosal ulceration (mouth sores). - Decreased blood cell counts (anemia, leukopenia, thrombocytopenia). - Elevated liver enzymes. - Hair thinning or loss.

Serious or Rare Side Effects: - Severe liver toxicity or hepatic fibrosis. - Pulmonary fibrosis or interstitial pneumonitis. - Life‑threatening infections due to bone‑marrow suppression. - Marked bone‑marrow failure leading to pancytopenia. - Acute renal failure. - Severe cutaneous reactions such as Stevens‑Johnson syndrome.

What precautions apply to Methotrexate?

Before initiating Methofill, several safety considerations should be addressed. - Monitor liver function: perform baseline and periodic hepatic enzyme tests. - Assess renal function: adjust dose or avoid use in significant impairment. - Screen for infections: avoid initiating therapy in active infections. - Avoid pregnancy: drug is teratogenic and contraindicated in pregnant women. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Methotrexate interact with?

Methofill interacts with several medicines that can alter its safety or efficacy.

Major Interactions (Avoid): - Nonsteroidal anti‑inflammatory drugs (NSAIDs): increase risk of renal and hepatic toxicity. - Live vaccines: heightened risk of severe infection. - Trimethoprim‑sulfamethoxazole: potentiates bone‑marrow suppression. - Aminoglycoside antibiotics: may exacerbate nephrotoxicity.

Moderate Interactions (Monitor Closely): - Proton pump inhibitors: may affect absorption and bioavailability. - Phenytoin: can reduce methotrexate efficacy. - Alcohol: increases risk of liver injury.

Frequently asked questions

What conditions is Methofill used to treat?+
Methofill is indicated for the management of rheumatoid arthritis, severe plaque psoriasis, certain malignancies such as acute lymphoblastic leukemia and non‑Hodgkin lymphoma, and for medical termination of ectopic pregnancy. In each case the drug works by suppressing abnormal cell growth or immune activity that drives disease.
How does methotrexate, the active ingredient in Methofill, work?+
Methotrexate blocks the enzyme dihydrofolate reductase, which is essential for converting folate into its active form. This inhibition reduces the synthesis of DNA, RNA, and proteins, limiting the proliferation of rapidly dividing cells, including immune cells and cancer cells, thereby providing immunosuppressive and antiproliferative effects.
What is the usual dose of Methofill?+
The dosage of Methofill is individualized and determined by the prescribing clinician based on the specific indication, patient weight, renal and hepatic function, and response to therapy. Patients should follow the exact dosing schedule provided by their healthcare professional and not adjust the dose on their own.
Is Methofill safe to use during pregnancy or while breastfeeding?+
Methofill is classified as Pregnancy Category X, meaning it is contraindicated in pregnancy because it can cause severe fetal malformations or death. It is also not recommended during breastfeeding, as methotrexate can be excreted in breast milk and may harm the infant. Effective contraception is required for both men and women receiving the drug.
How do I order Methofill from GNH USA?+
To place an order, visit the product page for Methofill on gnh-usa.com, enter the required quantity, and submit the inquiry form. 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 the same conditions?+
For rheumatoid arthritis, Methofill (methotrexate) is often the first‑line disease‑modifying antirheumatic drug (DMARD) and is less expensive than many biologic agents. In oncology, it offers a non‑targeted chemotherapy option that can be combined with newer agents. Compared with newer oral DMARDs, methotrexate has a longer safety record but requires regular monitoring of liver and blood parameters.
What are the storage and handling requirements for Methofill?+
Methofill should be stored in a refrigerator at 2‑8 °C (36‑46 °F). Keep the vial in its original packaging, protect it from light, and do not freeze or shake the product. If temporary storage at room temperature is unavoidable, limit exposure to no more than 24 hours and return it to refrigeration promptly.
How is Methofill administered to patients?+
Methofill is supplied as a sterile solution for subcutaneous injection. A healthcare professional administers the dose using a suitable needle and syringe, typically into the abdomen or thigh. The injection site should be rotated to reduce local irritation, and patients should be instructed on proper aseptic technique if self‑administration is approved.
What are the most serious risks associated with Methofill?+
The most critical adverse events include severe liver toxicity, pulmonary fibrosis, profound bone‑marrow suppression leading to pancytopenia, and life‑threatening infections. Renal failure and rare severe skin reactions such as Stevens‑Johnson syndrome may also occur. Prompt recognition and medical evaluation of these signs are essential for patient safety.
Who should not use Methofill?+
Methofill is contraindicated in pregnant women, individuals with known hypersensitivity to methotrexate or any component of the formulation, patients with severe hepatic impairment, uncontrolled infections, and those with significant renal dysfunction. Caution is also advised for patients with pre‑existing lung disease or a history of severe bone‑marrow suppression.
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 B.V.
Origin
EU

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