Europe — EMA
Metoject
GNH USA supplies Metoject (Methotrexate), an antimetabolite for rheumatoid arthritis, psoriasis, leukemia and lymphoma. Request a quote for global supply.
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What is Methotrexate?
Methotrexate, the active ingredient in Metoject, is an antimetabolite presented as an injection for intramuscular, intravenous, and subcutaneous use. It is approved in the European Union and classified as prescription‑only. The drug works by interfering with folate metabolism, which limits rapid cell proliferation.
GNH USA supplies Metoject as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide and adheres to stringent quality standards.
What is Methotrexate used for?
Methotrexate is used in several autoimmune and oncologic conditions that involve abnormal cell proliferation.
Rheumatoid arthritis: reduces joint inflammation and slows disease progression. Psoriasis: improves skin lesions and decreases plaque formation. Acute lymphoblastic leukemia: induces remission by inhibiting malignant lymphoblast growth. Non‑Hodgkin lymphoma: contributes to tumor control as part of combination chemotherapy. Gestational trophoblastic disease: eradicates trophoblastic tissue and prevents disease recurrence.
What are the side effects of Methotrexate?
Methotrexate may cause a range of adverse reactions, varying from mild to severe.
Common Side Effects: - Nausea and vomiting - Fatigue or weakness - Oral ulcers or mucositis - Mild elevation of liver enzymes - Decreased white blood cell count - Headache
Serious or Rare Side Effects: - Severe liver toxicity or hepatitis - Pulmonary fibrosis or interstitial pneumonitis - Bone marrow aplasia leading to pancytopenia - Life‑threatening infections - Acute renal failure - Cutaneous necrosis or severe skin reactions
What precautions apply to Methotrexate?
When using Metoject, several precautions should be observed to minimize risk.
Pregnancy: contraindicated (Category X) – avoid use in pregnant patients. Renal impairment: assess kidney function before initiation and adjust as needed. Hepatic impairment: monitor liver enzymes regularly during therapy. Hematologic monitoring: perform complete blood counts frequently to detect bone‑marrow suppression. Drug interactions: review concomitant medications for potential additive toxicity. Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.
What does Methotrexate interact with?
Methotrexate can interact with other medicines, altering its efficacy or safety.
Major Interactions (Avoid): - Live vaccines: may cause severe infection. - NSAIDs: increase risk of hematologic toxicity. - Trimethoprim‑sulfamethoxazole: enhances myelosuppression. - Pemetrexed: additive antimetabolite effects. - Proton pump inhibitors: may affect absorption (rare).
Moderate Interactions (Monitor Closely): - Penicillins: possible increased toxicity. - Sulfonamides: may augment bone‑marrow suppression. - Alcohol: heightens liver toxicity risk. - Phenytoin: may reduce methotrexate clearance. - Azathioprine: combined immunosuppression requires monitoring.
Frequently asked questions
What conditions is Metoject used to treat?+
How does methotrexate work in the body?+
What determines the dose of Metoject?+
Is Metoject safe during pregnancy or breastfeeding?+
How do I order Metoject from GNH USA?+
How does Metoject compare with other antimetabolites?+
What are the recommended storage conditions for Metoject?+
How is Metoject administered to patients?+
What are the most serious risks associated with Metoject?+
Who should not use Metoject?+
Product details
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