GNH USA

Europe — EMA

Methofill

GNH USA supplies Methofill (Methotrexate), an antirheumatic drug for rheumatoid arthritis, psoriasis and selected cancers. 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. Classified as a disease‑modifying antirheumatic drug (DMARD), it is indicated for rheumatoid arthritis, psoriasis, selected cancers and ectopic pregnancy, and is marketed in the European Union.

GNH USA supplies Methofill as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring quality assurance, regulatory conformity and reliable cold‑chain logistics.

What is Methotrexate used for?

Methofill (methotrexate) is used in conditions where inhibition of rapidly dividing cells or immune modulation is required.

- Rheumatoid arthritis: reduces joint inflammation and slows disease progression. - Psoriasis: decreases skin plaque formation and severity. - Acute lymphoblastic leukemia: interferes with malignant cell proliferation. - Non‑Hodgkin lymphoma: contributes to tumor control. - Ectopic pregnancy: terminates trophoblastic tissue.

What are the side effects of Methotrexate?

Methofill may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects: - Nausea: mild gastrointestinal upset. - Fatigue: reduced energy levels. - Mouth sores: oral ulceration. - Elevated liver enzymes: mild hepatic enzyme rise.

Serious or Rare Side Effects: - Bone marrow suppression: pancytopenia, increased infection risk. - Pulmonary toxicity: interstitial pneumonitis or fibrosis. - Severe hepatic injury: hepatitis or liver failure.

What precautions apply to Methotrexate?

When prescribing Methofill, clinicians should observe several safety precautions to minimize risk.

- Renal function: assess creatinine clearance before initiation and monitor regularly. - Hepatic status: evaluate liver enzymes and avoid use in severe hepatic impairment. - Pregnancy: contraindicated in pregnancy (Category X); ensure effective contraception. - Infections: screen for latent tuberculosis and avoid use in active infections. - Drug monitoring: perform complete blood counts frequently to detect marrow suppression. - 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 its efficacy or safety profile.

Major Interactions (Avoid): - Non‑steroidal anti‑inflammatory drugs (NSAIDs): increase risk of renal toxicity. - High‑dose penicillins: may reduce methotrexate clearance, raising toxicity. - Proton pump inhibitors (omeprazole): can impair renal elimination, enhancing toxicity.

Moderate Interactions (Monitor Closely): - Sulfonamides: may potentiate myelosuppression. - Trimethoprim‑sulfamethoxazole: increased risk of bone marrow suppression. - Azathioprine: additive immunosuppression. - Live vaccines: heightened infection risk.

Frequently asked questions

What conditions is Methofill used to treat?+
Methofill contains methotrexate and is prescribed for rheumatoid arthritis, plaque psoriasis, certain cancers such as acute lymphoblastic leukemia and non‑Hodgkin lymphoma, and for medical management of ectopic pregnancy. It works by modulating immune activity and inhibiting cell proliferation in these disease states.
How does methotrexate work in the body?+
Methotrexate is a folate antagonist that blocks dihydrofolate reductase, preventing the formation of tetrahydrofolate needed for DNA synthesis. This reduces the proliferation of rapidly dividing cells and suppresses immune cell activity, providing anti‑inflammatory and immunosuppressive effects useful in autoimmune disorders and cancer.
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 can determine the appropriate dosing regimen.
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 while breastfeeding, as methotrexate can be excreted in breast milk and may affect the infant.
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 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 Methofill compare with other DMARDs?+
Methofill (methotrexate) is often considered a first‑line disease‑modifying antirheumatic drug because of its proven efficacy, oral or injectable formulations, and cost‑effectiveness. Compared with biologic DMARDs, it has a broader mechanism affecting cell proliferation and may be used alone or in combination, but it requires careful monitoring for toxicity.
What are the storage and handling requirements for Methofill?+
Methofill should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. Keep the product in its original packaging until use to maintain stability and ensure proper temperature control during transport.
How is Methofill administered?+
Methofill is supplied as a sterile solution for subcutaneous injection. The injection is typically given by a healthcare professional or trained patient, using aseptic technique, into the subcutaneous tissue of the abdomen, thigh or upper arm as directed by the prescriber.
What are the most serious risks associated with Methofill?+
The most serious risks include bone marrow suppression leading to pancytopenia, severe hepatic injury such as hepatitis or liver failure, and pulmonary toxicity that can progress to interstitial pneumonitis or fibrosis. Prompt monitoring of blood counts, liver function and respiratory status is essential.
Who should not use Methofill?+
Methofill is contraindicated in patients who are pregnant, have severe renal or hepatic impairment, have active infections, or have known hypersensitivity to methotrexate or any component of the formulation. Caution is also advised in individuals with pre‑existing blood dyscrasias.
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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