GNH USA

Europe — EMA

Metojectpen

GNH USA supplies Metojectpen (Methotrexate), a folate antagonist DMARD and antineoplastic agent for rheumatoid arthritis, severe plaque psoriasis and certain

Methotrexate

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What is Methotrexate?

Methotrexate, the active ingredient in Metojectpen, is an antimetabolite (folate antagonist) presented as a pre‑filled subcutaneous injection pen for subcutaneous use. It treats rheumatoid arthritis, severe plaque psoriasis, juvenile idiopathic arthritis, and certain malignancies such as acute lymphoblastic leukemia and lymphoma.

GNH USA supplies Metojectpen as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies, oncology centres and clinics worldwide. The company ensures consistent quality and regulatory compliance across a broad range of therapeutic areas, with reliable logistics and support for clinical programs.

What is Methotrexate used for?

Methotrexate is used as a disease‑modifying antirheumatic drug (DMARD) and antineoplastic agent to manage inflammatory and malignant conditions. - Rheumatoid arthritis: reduces joint inflammation and slows structural damage. - Severe plaque psoriasis: decreases skin lesions and plaque formation. - Juvenile idiopathic arthritis: controls disease activity and improves joint function. - Acute lymphoblastic leukemia: interferes with malignant cell proliferation. - Lymphoma: inhibits growth of malignant lymphoid cells.

What are the side effects of Methotrexate?

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

Common Side Effects: - Nausea or vomiting. - Fatigue or weakness. - Mouth ulcers or stomatitis. - Elevated liver enzymes.

Serious or Rare Side Effects: - Severe liver toxicity, including hepatitis or fibrosis. - Pulmonary toxicity such as interstitial pneumonitis. - Bone marrow suppression leading to severe infection, anemia or thrombocytopenia.

What precautions apply to Methotrexate?

Before initiating therapy, clinicians should assess baseline organ function and counsel patients on potential risks. - Monitor liver function: perform regular hepatic enzyme tests. - Monitor blood counts: check complete blood count frequently. - Avoid use in pregnancy: methotrexate is teratogenic (Category X). - Use caution in renal impairment: adjust dosing as needed. - Counsel on infection signs: advise immediate medical attention for fever or unexplained illness. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Methotrexate interact with?

Methotrexate interacts with several medicines that can alter its safety or efficacy.

Major Interactions (Avoid): - Non‑steroidal anti‑inflammatory drugs (NSAIDs): increase methotrexate toxicity. - Trimethoprim‑sulfamethoxazole: heightens risk of bone‑marrow suppression. - Live vaccines: may cause severe infection due to immunosuppression.

Moderate Interactions (Monitor Closely): - Azathioprine: additive immunosuppressive effect, monitor blood counts. - Allopurinol: may increase methotrexate levels, watch for toxicity. - Phenytoin: can reduce methotrexate clearance, adjust monitoring accordingly.

Frequently asked questions

What conditions is Metojectpen used to treat?+
Metojectpen contains methotrexate and is indicated for rheumatoid arthritis, severe plaque psoriasis, juvenile idiopathic arthritis, and certain cancers such as acute lymphoblastic leukemia and lymphoma. It is prescribed when disease‑modifying therapy is required to control inflammation or to inhibit malignant cell growth.
How does methotrexate work in the body?+
Methotrexate blocks the enzyme dihydrofolate reductase, reducing tetrahydrofolate production. This limits synthesis of DNA, RNA and proteins in rapidly dividing cells, which curtails cancer cell proliferation. In rheumatic diseases, it also raises extracellular adenosine levels, providing anti‑inflammatory effects.
What determines the dose of Metojectpen?+
The exact dose of Metojectpen is individualized by the prescribing clinician based on the patient’s disease severity, weight, renal and hepatic function, and response to therapy. Dosing regimens vary between rheumatologic and oncologic indications, and the prescriber will set the appropriate schedule.
Is Metojectpen safe during pregnancy or breastfeeding?+
Methotrexate is classified as Pregnancy Category X because it is known to cause fetal malformations and embryotoxicity. It is contraindicated in pregnancy and should be stopped well before conception. Breastfeeding is also not recommended, as methotrexate can be excreted in milk and affect the infant.
How do I order Metojectpen from GNH USA?+
To request Metojectpen, 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 any required import documentation.
How does Metojectpen compare with other DMARDs or biologics?+
Metojectpen (methotrexate) is a conventional synthetic DMARD, offering oral‑like convenience in an injectable pen and a well‑established safety profile. Biologic DMARDs target specific cytokines (e.g., TNF‑α inhibitors) and may be used when methotrexate alone is insufficient, but they are generally more expensive and require more intensive monitoring.
What are the storage and handling requirements for Metojectpen?+
Metojectpen should be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze or shake the pen. If the product must be transported, maintain the cold chain using validated insulated containers and temperature monitors to preserve drug stability.
How is Metojectpen administered to patients?+
Metojectpen is a pre‑filled pen designed for subcutaneous injection. The prescriber or trained healthcare professional selects the prescribed dose, cleans the injection site, and presses the pen to deliver the medication into the subcutaneous tissue, typically in the abdomen or thigh.
What are the most serious risks associated with Metojectpen?+
The most serious risks include severe liver toxicity, pulmonary fibrosis or interstitial pneumonitis, and profound bone‑marrow suppression that can lead to life‑threatening infections, anemia or bleeding. Patients should be monitored regularly for liver enzymes, lung symptoms and complete blood counts.
Who should not use Metojectpen?+
Metojectpen is contraindicated in pregnant women, individuals with severe hepatic or renal impairment, and patients with known hypersensitivity to methotrexate or any component of the formulation. Caution is also advised for those with active infections, immunodeficiency, or a history of pulmonary disease.
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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