GNH USA

Europe — EMA

Metoject

GNH USA supplies Metoject (Methotrexate), an antimetabolite for rheumatoid arthritis, psoriasis, leukemia and lymphoma. Request a quote for global supply.

Methotrexate

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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?+
Metoject, containing methotrexate, is indicated for several autoimmune and oncologic disorders. It is commonly prescribed for rheumatoid arthritis and severe plaque psoriasis, as well as for hematologic cancers such as acute lymphoblastic leukemia and non‑Hodgkin lymphoma. Additionally, it is used in the management of gestational trophoblastic disease to eliminate abnormal trophoblastic tissue.
How does methotrexate work in the body?+
Methotrexate blocks the enzyme dihydrofolate reductase, which is essential for converting folic acid into its active form. By inhibiting this step, the drug reduces the synthesis of purine nucleotides and thymidylate, leading to decreased DNA, RNA and protein production. This effect is most pronounced in rapidly dividing cells, such as immune cells and malignant tumor cells, thereby reducing inflammation and tumor growth.
What determines the dose of Metoject?+
The dose of Metoject is individualized by the prescribing clinician based on the specific indication, disease severity, patient weight, renal and hepatic function, and response to therapy. Because dosing varies widely across conditions—from low weekly doses for rheumatoid arthritis to higher, intermittent doses for oncology protocols—the prescriber sets the exact regimen and monitors the patient closely.
Is Metoject safe during pregnancy or breastfeeding?+
Metoject is classified as Pregnancy Category X, meaning it is contraindicated in pregnancy due to a high risk of fetal malformations and embryotoxicity. It should not be used by women who are pregnant or planning to become pregnant. Breastfeeding is also discouraged because methotrexate can be excreted in breast milk and may harm the infant.
How do I order Metoject from GNH USA?+
To request Metoject, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams across international markets. After the enquiry, the sales team will verify trade or institutional credentials, then provide pricing, availability, shipping details—including cold‑chain handling if needed—and assist with any required import documentation.
How does Metoject compare with other antimetabolites?+
Metoject (methotrexate) is one of the most widely used antimetabolites, distinguished by its oral and injectable formulations and a broad therapeutic spectrum that includes both autoimmune diseases and cancers. Compared with newer agents such as pemetrexed or leflunomide, methotrexate has a longer safety record but may require more intensive monitoring for hepatic and hematologic toxicity. Choice of therapy depends on disease type, patient factors and clinician experience.
What are the recommended storage conditions for Metoject?+
Metoject should be stored at 2‑8 °C (refrigerated). Keep the vials in their original packaging, protect them from light, and avoid freezing or shaking the solution. If the product must be transported, use validated cold‑chain containers to maintain the temperature range throughout the journey.
How is Metoject administered to patients?+
Metoject is supplied as a sterile injection that can be given intramuscularly, intravenously, or subcutaneously, depending on the clinical indication and physician preference. The route, volume and rate of administration are determined by the prescriber. In oncology settings, the injection is often given as a short infusion, whereas for rheumatic diseases it may be administered as a quick intramuscular or subcutaneous injection.
What are the most serious risks associated with Metoject?+
The most serious risks include severe liver toxicity, which can progress to hepatitis or cirrhosis; pulmonary complications such as interstitial pneumonitis or fibrosis; profound bone‑marrow suppression leading to pancytopenia; and life‑threatening infections due to immunosuppression. Renal failure and rare cutaneous necrosis are also reported. Patients should be monitored regularly for early signs of these complications.
Who should not use Metoject?+
Metoject is contraindicated in pregnant women, individuals with known hypersensitivity to methotrexate or any component of the formulation, and patients with severe hepatic or renal impairment that cannot be corrected. It should also be avoided in patients receiving live vaccines or those with uncontrolled infections. Clinicians must evaluate each patient’s medical history before initiating therapy.
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
Intramuscular Use , Intravenous Use , Subcutaneous
Manufacturer
Medac Gesellschaft Für Klinische Spezialpräparate Mbh (Wedel)
Origin
EU

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