GNH USA

Europe — EMA

Metoject Pen

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

Methotrexate

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What is Methotrexate?

Methotrexate, the active ingredient in Metoject Pen, is an antimetabolite presented as a pre‑filled pen for subcutaneous injection. It is used to treat rheumatoid arthritis, psoriasis, acute lymphoblastic leukemia and other autoimmune conditions.

GNH USA supplies Metoject Pen as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing reliable access to this essential immunosuppressant for qualified healthcare providers and supporting therapeutic programs across multiple therapeutic areas. Our global logistics network ensures timely delivery and compliance with local regulatory requirements.

What is Methotrexate used for?

Methotrexate is employed in several autoimmune and oncologic disease pathways to modulate immune activity and cell proliferation. - Rheumatoid arthritis: reduces joint inflammation and slows disease progression. - Psoriasis: improves skin lesions and decreases plaque formation. - Acute lymphoblastic leukemia: interferes with malignant cell replication as part of chemotherapy protocols. - Other autoimmune conditions: provides disease control in severe inflammatory disorders such as inflammatory bowel disease.

What are the side effects of Methotrexate?

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

Common Side Effects: - Nausea or vomiting - Fatigue - Mouth sores (stomatitis) - Mild liver enzyme elevation

Serious or Rare Side Effects: - Severe liver toxicity or fibrosis - Pulmonary fibrosis or interstitial pneumonitis - Renal impairment - Severe bone marrow suppression (pancytopenia)

What precautions apply to Methotrexate?

Use of Metoject Pen requires careful monitoring and adherence to safety guidelines. - Pregnancy: contraindicated; teratogenic risk classified as Category X. - Liver function: monitor hepatic enzymes regularly; avoid in pre‑existing liver disease. - Renal function: assess creatinine clearance before initiation and during therapy. - Blood counts: perform complete blood count monitoring to detect cytopenias. - Concomitant immunosuppressants: evaluate risk of additive immunosuppression. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Methotrexate interact with?

Methotrexate interacts with several drug classes; awareness of these interactions helps prevent toxicity.

Major Interactions (Avoid): - Non‑steroidal anti‑inflammatory drugs (NSAIDs): increase methotrexate toxicity. - Proton pump inhibitors (e.g., omeprazole): may raise serum levels. - Trimethoprim‑sulfamethoxazole: risk of severe bone marrow suppression. - Live vaccines: heightened infection risk.

Moderate Interactions (Monitor Closely): - Penicillins and other antibiotics: may affect renal clearance. - Sulfonylureas: potential for enhanced hypoglycemia. - Alcohol: adds to hepatic stress.

Frequently asked questions

What conditions is Metoject Pen used to treat?+
Metoject Pen delivers methotrexate, which is approved for rheumatoid arthritis, moderate to severe plaque psoriasis, acute lymphoblastic leukemia, and other severe autoimmune disorders where conventional therapy is insufficient.
How does methotrexate work?+
Methotrexate blocks the enzyme dihydrofolate reductase, reducing the production of tetrahydrofolate needed for DNA and RNA synthesis. This antiproliferative effect limits the growth of rapidly dividing immune and cancer cells and also dampens inflammatory pathways.
What determines the dose of Metoject Pen?+
The dose of Metoject Pen is individualized by the prescribing clinician based on the specific indication, disease severity, patient weight, renal and hepatic function, and response to therapy. No fixed regimen is provided here.
Is Metoject Pen safe during pregnancy or breastfeeding?+
Methotrexate is classified as Pregnancy Category X because it is teratogenic and can cause fetal harm. It is contraindicated during pregnancy and should not be used while breastfeeding, as it can be excreted in milk.
How do I order Metoject Pen from GNH USA?+
To order, submit an enquiry on the Metoject Pen 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 where required) and import documentation.
How does Metoject Pen compare with other immunosuppressants?+
Compared with agents such as leflunomide or biologic TNF inhibitors, methotrexate offers a well‑established oral and subcutaneous route, a broad therapeutic window, and lower acquisition cost, but it requires regular laboratory monitoring for hepatic, renal and hematologic safety.
What are the recommended storage conditions for Metoject Pen?+
Metoject Pen should be stored at 2‑8 °C (refrigerated). Keep the pen in its original packaging, protect it from light, and do not freeze or shake the device. Do not use if the pen has been exposed to temperatures outside this range.
How is Metoject Pen administered?+
Metoject Pen is a pre‑filled, single‑use device for subcutaneous injection. The patient or healthcare professional removes the protective cap, selects the appropriate injection site (typically the abdomen or thigh), and presses the plunger to deliver the prescribed dose.
What are the most serious risks to watch for while using Metoject Pen?+
Serious risks include severe liver toxicity, pulmonary fibrosis or interstitial pneumonitis, renal impairment, and profound bone marrow suppression leading to pancytopenia. Patients should report symptoms such as persistent nausea, shortness of breath, jaundice, or unusual bruising immediately.
Who should not use Metoject Pen?+
Metoject Pen is contraindicated in pregnant or nursing women, patients with known hypersensitivity to methotrexate, those with severe hepatic or renal disease, and individuals receiving live vaccines. Caution is also advised for patients with 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
Medac Gesellschaft Für Klinische Spezialpräparate Mbh (Wedel)
Origin
EU

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