GNH USA

Europe — EMA

Methofill

GNH USA supplies Methofill (Methotrexate), an antimetabolite DMARD for rheumatoid arthritis, psoriasis, psoriatic arthritis, acute lymphoblastic leukemia

Methotrexate

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What is Methotrexate?

Methotrexate, the active ingredient in Methofill, is an antimetabolite presented as a sterile solution for injection for subcutaneous use. It is employed in the management of autoimmune disorders and certain cancers, specifically rheumatoid arthritis, psoriasis, psoriatic arthritis, acute lymphoblastic leukemia, and gestational trophoblastic disease, providing disease‑modifying benefits.

GNH USA supplies Methofill as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring quality and regulatory compliance across global markets.

What is Methotrexate used for?

Methotrexate is indicated for several autoimmune and oncologic conditions where it modulates cell proliferation and inflammation.

- Rheumatoid arthritis: reduces joint inflammation and slows disease progression. - Psoriasis: improves skin lesions and decreases scaling. - Psoriatic arthritis: alleviates joint pain while treating skin symptoms. - Acute lymphoblastic leukemia: induces remission by inhibiting rapidly dividing leukemic cells. - Gestational trophoblastic disease: promotes resolution of abnormal trophoblastic tissue.

What are the side effects of Methotrexate?

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

Common Side Effects: - Nausea and vomiting. - Oral mucosal ulceration. - Fatigue or mild weakness. - Transient elevation of liver enzymes.

Serious or Rare Side Effects: - Bone marrow suppression leading to pancytopenia. - Severe hepatotoxicity or fibrosis. - Pulmonary toxicity, including interstitial pneumonitis. - Life‑threatening infections due to immunosuppression.

What precautions apply to Methotrexate?

Use of Methofill requires careful monitoring and specific safety measures.

- Liver monitoring: obtain baseline liver function tests and repeat periodically. - Hematologic monitoring: perform regular complete blood counts to detect marrow suppression. - Renal function: assess creatinine clearance before initiation and during therapy. - Pregnancy contraindication: avoid use in pregnant or planning‑to‑be‑pregnant patients (Category X). - Infection risk: counsel patients to report signs of infection promptly. - 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, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid): - Non‑steroidal anti‑inflammatory drugs (NSAIDs): increase risk of nephrotoxicity and gastrointestinal toxicity. - Other folate antagonists (e.g., trimethoprim): potentiate hematologic toxicity.

Moderate Interactions (Monitor Closely): - Proton pump inhibitors: may alter methotrexate clearance. - Azathioprine or other immunosuppressants: increase risk of bone marrow suppression. - Warfarin: may enhance anticoagulant effect, requiring INR monitoring.

Frequently asked questions

What conditions is Methofill used for?+
Methofill contains methotrexate and is prescribed for several autoimmune and oncologic conditions. It is used to manage rheumatoid arthritis, psoriasis, psoriatic arthritis, acute lymphoblastic leukemia, and gestational trophoblastic disease, providing disease‑modifying benefits in each indication.
How does methotrexate work in the body?+
Methotrexate blocks the enzyme dihydrofolate reductase, preventing the formation of tetrahydrofolate needed for purine and pyrimidine synthesis. This halts DNA, RNA, and protein production in rapidly dividing cells and also increases adenosine release, which reduces inflammation and suppresses immune activity.
What is the usual dose of Methofill?+
The dose of Methofill is individualized. A qualified prescriber determines the appropriate amount, frequency, and duration based on the specific indication, patient characteristics, and clinical response. No standard dosing regimen is provided here.
Is Methofill safe during pregnancy or breastfeeding?+
Methofill is classified as Pregnancy Category X, meaning it is contraindicated in pregnancy because it can cause fetal harm. It is also not recommended for breastfeeding mothers, as methotrexate can be excreted in breast milk and affect the infant.
How do I order Methofill from GNH USA?+
To order 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 necessary import documentation.
How does Methofill compare with other DMARDs or biologics?+
Methofill (methotrexate) is a conventional synthetic DMARD that is less expensive and orally or subcutaneously administered, unlike many biologics that require intravenous infusion. While biologics target specific cytokines, methotrexate has a broader anti‑inflammatory effect and is often used as first‑line therapy before escalating to biologic agents.
What are the storage and handling requirements for Methofill?+
Methofill should 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 temperature excursions occur, discard the product according to local regulations.
How is Methofill administered?+
Methofill is supplied as a sterile solution for subcutaneous injection. The injection is typically given into the abdomen or thigh using a suitable needle, following aseptic technique. Patients or healthcare professionals should rotate injection sites to reduce local irritation.
What are the most serious risks associated with Methofill?+
The most serious risks include bone marrow suppression leading to pancytopenia, severe hepatotoxicity or liver fibrosis, and pulmonary toxicity such as interstitial pneumonitis. These adverse events require regular laboratory monitoring and immediate medical attention if symptoms arise.
Who should not use Methofill?+
Methofill should not be used by pregnant or breastfeeding women, patients with severe renal impairment, those with pre‑existing liver disease, or individuals with known hypersensitivity to methotrexate or any component of the formulation. Caution is also advised for patients with active infections.
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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