GNH USA

Europe — EMA

Methofill

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

Methotrexate

Request sourcing

1
Pack/s

What is Methotrexate?

Methotrexate, the active ingredient in Methofill, is an antimetabolite (folate antagonist) presented as a subcutaneous formulation for subcutaneous use. It is employed to treat autoimmune disorders such as rheumatoid arthritis and psoriasis, as well as certain cancers including acute lymphoblastic leukemia and non‑Hodgkin lymphoma. GNH USA supplies Methofill as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Methotrexate used for?

Methofill, a folate antagonist, is used across several disease families where it modulates immune activity or inhibits malignant cell growth. - Rheumatoid arthritis: reduces disease activity and joint damage in adult patients. - Psoriasis: improves skin lesions and decreases severity. - Acute lymphoblastic leukemia: induces remission by targeting rapidly dividing lymphoblasts. - Non‑Hodgkin lymphoma: contributes to tumor control as part of combination regimens. - Other malignancies requiring antimetabolite therapy: provides cytotoxic effect in various solid and hematologic cancers.

What are the side effects of Methotrexate?

Methofill may cause a range of adverse reactions, from mild to life‑threatening.

Common Side Effects: - Nausea and vomiting. - Fatigue or malaise. - Mucositis or oral ulceration. - Elevated liver enzymes. - Alopecia (hair loss). - Headache.

Serious or Rare Side Effects: - Bone marrow suppression leading to pancytopenia. - Severe hepatic toxicity or fibrosis. - Pulmonary fibrosis or interstitial pneumonitis. - Acute renal failure. - Life‑threatening infections. - Teratogenic effects causing fetal malformations.

What precautions apply to Methotrexate?

Methofill requires careful monitoring and specific safety measures before and during therapy. - Pregnancy: contraindicated (Category X); avoid use in pregnant patients. - Renal function: assess baseline and monitor; adjust dose if impairment is present. - Liver function: regularly check hepatic enzymes and bilirubin. - Hematologic monitoring: perform complete blood counts to detect marrow suppression. - Infection risk: defer treatment in active infections and monitor for opportunistic infections. - 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 drug classes, altering its safety profile.

Major Interactions (Avoid): - Non‑steroidal anti‑inflammatory drugs (NSAIDs): increase methotrexate toxicity. - Penicillins (e.g., ampicillin): reduce renal clearance, raising drug levels. - Alcohol: potentiates hepatotoxicity.

Moderate Interactions (Monitor Closely): - Sulfonamides: may increase methotrexate toxicity. - Trimethoprim‑sulfamethoxazole: similar risk of enhanced adverse effects.

Frequently asked questions

What conditions is Methofill used to treat?+
Methofill contains methotrexate, which is prescribed for autoimmune diseases such as rheumatoid arthritis and psoriasis, as well as for certain cancers including acute lymphoblastic leukemia and non‑Hodgkin lymphoma. It may also be used in other malignancies that require antimetabolite therapy.
How does methotrexate work in the body?+
Methotrexate blocks the enzyme dihydrofolate reductase, reducing tetrahydrofolate production. This limits the synthesis of nucleotides needed for DNA, RNA and protein formation, suppressing rapidly dividing cells and, at lower doses, dampening inflammatory pathways.
What is the usual dose of Methofill?+
The dose of Methofill is individualized by the prescribing clinician based on the specific indication, patient characteristics, and laboratory monitoring. Dosage regimens are not standardized and should follow the prescriber’s instructions.
Is Methofill safe during pregnancy or breastfeeding?+
Methofill is classified as Pregnancy Category X, meaning it is contraindicated in pregnancy due to a high risk of fetal malformations. It is also not recommended while breastfeeding because it can be excreted in milk and 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 works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed) and import documentation.
How does Methofill compare with other immunosuppressants?+
Methofill (methotrexate) is a folate antagonist, differing from biologic agents that target specific cytokines. It is generally less expensive, administered via subcutaneous injection, and has a well‑characterized safety profile, but requires regular monitoring of blood counts and liver function, unlike some newer biologics.
What are the storage and handling requirements for Methofill?+
Methofill should be stored at 2‑8 °C, kept refrigerated, protected from light, and never frozen or shaken. Maintain the product in its original packaging until use to preserve stability.
How is Methofill administered?+
Methofill is given by subcutaneous injection, typically into the abdomen or thigh. The injection site should be rotated to reduce local irritation, and the medication must be prepared according to aseptic technique as instructed by the healthcare professional.
What are the most serious risks associated with Methofill?+
The most serious risks include bone marrow suppression leading to pancytopenia, severe liver toxicity, pulmonary fibrosis, acute renal failure, life‑threatening infections, and teratogenic effects that can cause fetal malformations if exposure occurs during pregnancy.
Who should not use Methofill?+
Methofill is contraindicated in pregnant women, individuals with severe renal or hepatic impairment, patients with active infections, and those with known hypersensitivity to methotrexate or any component of the formulation.
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

Related products