GNH USA

Europe — EMA

Metoject

GNH USA supplies Metoject (Methotrexate), an antimetabolite for rheumatoid arthritis, psoriasis, and certain cancers including acute lymphoblastic leukemia

Methotrexate

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What is Methotrexate?

Methotrexate, the active ingredient in Metoject, is an antimetabolite presented as an injectable solution for intramuscular, intravenous, or subcutaneous use. It is employed in the management of rheumatoid arthritis, psoriasis, and selected malignancies such as acute lymphoblastic leukemia, non‑Hodgkin lymphoma, and breast cancer in both adult and pediatric patients.

GNH USA supplies Metoject as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, and pharmacies worldwide, providing reliable sourcing, regulatory support, and cold‑chain logistics for this injectable chemotherapy and immunosuppressant agent.

What is Methotrexate used for?

Methotrexate is an antimetabolite used to modulate immune activity and inhibit cancer cell proliferation.

- Rheumatoid arthritis: reduces joint inflammation and slows disease progression. - Psoriasis: diminishes skin lesions and plaque formation. - Acute lymphoblastic leukemia: interferes with malignant cell replication. - Non‑Hodgkin lymphoma: impedes tumor growth. - Breast cancer: enhances the effectiveness of combination chemotherapy. - Ectopic pregnancy: terminates trophoblastic tissue when surgery is not feasible.

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 malaise. - Mouth sores (stomatitis). - Mild elevation of liver enzymes. - Temporary hair thinning.

Serious or Rare Side Effects: - Severe liver toxicity or fibrosis. - Pulmonary fibrosis or interstitial pneumonitis. - Significant bone marrow suppression leading to infection or bleeding. - Acute renal failure. - Anaphylactic or severe hypersensitivity reactions.

What precautions apply to Methotrexate?

Prior to initiating therapy, several safety measures should be observed.

- Monitor blood counts: perform regular CBC to detect cytopenias. - Assess liver function: check transaminases before and during treatment. - Avoid use in pregnancy: methotrexate is contraindicated and requires effective contraception. - Counsel on contraception: both male and female patients must use reliable methods. - Adjust dose in renal impairment: reduce dosage or increase monitoring as needed. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Methotrexate interact with?

Methotrexate can interact with several medicines, altering its efficacy or toxicity.

Major Interactions (Avoid): - Non‑steroidal anti‑inflammatory drugs (NSAIDs): increase risk of renal toxicity. - Proton pump inhibitors (e.g., omeprazole): may raise methotrexate plasma levels. - Trimethoprim‑sulfamethoxazole: potentiates bone marrow suppression.

Moderate Interactions (Monitor Closely): - Azathioprine or other immunosuppressants: additive myelosuppression. - Live vaccines: risk of infection due to immunosuppression.

Frequently asked questions

What conditions is Metoject used to treat?+
Metoject, containing methotrexate, is prescribed for autoimmune disorders such as rheumatoid arthritis and psoriasis, as well as for certain cancers including acute lymphoblastic leukemia, non‑Hodgkin lymphoma, and breast cancer. It may also be used in the medical management of ectopic pregnancy when surgery is not an option.
How does methotrexate work in the body?+
Methotrexate blocks the enzyme dihydrofolate reductase, which is essential for converting folate into its active form. This inhibition disrupts the synthesis of nucleotides needed for DNA, RNA, and protein production, thereby limiting the proliferation of rapidly dividing immune cells and cancer cells.
What is the usual dose of Metoject?+
The specific dose of Metoject is determined by the prescribing clinician based on the patient’s condition, weight, renal function, and treatment goals. Dosage regimens vary widely between autoimmune indications and oncologic protocols, and the prescriber will tailor the schedule accordingly.
Is Metoject safe to use during pregnancy or while breastfeeding?+
Metoject is classified as pregnancy category X, meaning it is contraindicated in pregnancy due to a high risk of fetal malformations and miscarriage. It is also not recommended during breastfeeding because methotrexate can be excreted in breast milk and may harm the infant.
How do I order Metoject from GNH USA?+
To place an order, submit an enquiry on the Metoject 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 handling), and necessary import documentation.
How does Metoject compare with other chemotherapy agents?+
Metoject (methotrexate) is an antimetabolite that interferes with folate metabolism, whereas many other chemotherapy agents target microtubules, DNA cross‑linking, or kinase pathways. Methotrexate is often used in combination regimens because of its distinct mechanism, and it can be administered via injection, offering flexibility compared with oral formulations of other agents.
What are the storage requirements 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. Proper cold‑chain storage maintains drug stability and potency.
How is Metoject administered to patients?+
Metoject is supplied as an injectable solution and can be given intramuscularly, intravenously, or subcutaneously, depending on the clinical protocol. Administration is performed by a qualified healthcare professional under aseptic conditions, with dosage and frequency set by the treating physician.
What are the most serious risks associated with Metoject?+
The most serious risks include severe liver toxicity, pulmonary fibrosis, profound bone‑marrow suppression leading to infection or bleeding, acute renal failure, and life‑threatening hypersensitivity reactions. Patients should be monitored regularly for signs of organ dysfunction and blood‑cell abnormalities.
Who should not use Metoject?+
Metoject should not be used by pregnant women, individuals with known hypersensitivity to methotrexate, patients with severe liver disease, uncontrolled infections, or significant renal impairment without dose adjustment. It is also contraindicated in patients receiving live vaccines due to the risk of infection.
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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