Product image of Metex (Methotrexate) supplied by GNH India

Metex

Active Ingredient:
Methotrexate
Origin:
EU

Metex (Methotrexate)

Methotrexate, the active ingredient in Metex, is an Antimetabolite (folate antagonist) presented as a subcutaneous injection for subcutaneous use. It is employed in the management of rheumatoid arthritis, psoriasis, certain malignancies and ectopic pregnancy and is marketed in the European Union under EU regulatory standards.

GNH India supplies Metex as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Medac Gesellschaft Für Klinische Spezialpräparate Mbh (Wedel)

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Indications & Clinical Uses

  • Methotrexate is a folate antagonist used across several disease families.
  • Rheumatoid arthritis: reduces joint inflammation and slows structural damage.
  • Psoriasis: limits skin cell proliferation and improves plaque lesions.
  • Acute lymphoblastic leukemia and non‑Hodgkin lymphoma: interferes with malignant cell replication.
  • Ectopic pregnancy: medically terminates non‑viable implantation when surgery is not indicated.

How It Works

  • Methotrexate inhibits dihydrofolate reductase, preventing the conversion of dihydrofolate to tetrahydrofolate. This blockade reduces purine and pyrimidine synthesis, impairing DNA, RNA and protein production, which limits the proliferation of rapidly dividing cells such as immune cells and cancer cells.

Side Effects

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

Common Side Effects

  • Nausea or vomiting
  • Fatigue or malaise
  • Oral mucosal ulceration
  • Mild elevation of liver enzymes
  • Transient low white‑blood‑cell count
  • Temporary hair thinning

Serious or Rare Side Effects

  • Severe hepatotoxicity or fibrosis
  • Pulmonary fibrosis or interstitial pneumonitis
  • Life‑threatening bone‑marrow suppression
  • Acute renal failure
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis
  • Opportunistic infections due to immunosuppression

Precautions & Warnings

  • When using methotrexate, several safety considerations should be observed.
  • Pregnancy: contraindicated (Category X) – avoid use in women of childbearing potential without effective contraception.
  • Renal function: assess baseline creatinine and adjust dose in impairment.
  • Liver function: monitor transaminases regularly; avoid in pre‑existing severe hepatic disease.
  • Hematologic monitoring: perform complete blood counts before each dose to detect cytopenias.
  • Alcohol consumption: limit or avoid to reduce additional liver injury.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Methotrexate interacts with several medicines that may increase toxicity or reduce efficacy.

Major Interactions (Avoid)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) – increase methotrexate serum levels.
  • Proton‑pump inhibitors (e.g., omeprazole) – may raise toxicity.
  • Trimethoprim‑sulfamethoxazole – additive bone‑marrow suppression.
  • Live vaccines – risk of infection due to immunosuppression.
  • Gold salts – synergistic toxicity.

Moderate Interactions (Monitor Closely)

  • Azathioprine or cyclosporine – combined immunosuppression.
  • Penicillins (high‑dose) – possible reduced clearance.
  • Sulfonamide antibiotics – overlapping hematologic effects.
  • Folic acid supplements – may lessen efficacy if not properly timed.
  • Vitamin B12 – monitor for additive hematologic changes.

Frequently Asked Questions

Metex contains methotrexate, which is prescribed for rheumatoid arthritis, moderate to severe plaque psoriasis, certain hematologic cancers such as acute lymphoblastic leukemia and non‑Hodgkin lymphoma, and for medical management of ectopic pregnancy when surgery is not chosen.

Methotrexate blocks the enzyme dihydrofolate reductase, halting the formation of tetrahydrofolate needed for DNA, RNA and protein synthesis. This action suppresses rapidly dividing cells, including immune cells that drive inflammation and cancer cells that rely on folate metabolism.

The dose of Metex is individualized by the prescribing clinician based on the specific indication, patient weight, renal function and treatment response. Only a qualified health‑care professional should determine the appropriate dosing schedule.

Methotrexate is classified as Pregnancy Category X, meaning it is contraindicated in pregnancy because it can cause fetal malformations or death. It is also not recommended during breastfeeding, as it may be excreted in milk and affect the infant.

To order Metex, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India 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.

Compared with biologic DMARDs, methotrexate is an oral or injectable small‑molecule agent that is less expensive and has a well‑established efficacy profile. Unlike leflunomide, methotrexate has a broader oncologic use but may require more intensive laboratory monitoring for hepatic and hematologic toxicity.

Metex should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. Keep the product in its original packaging until use and discard any vial that shows particulate matter or discoloration.

Metex is supplied as a sterile solution for subcutaneous injection. It is typically administered by a health‑care professional or trained patient using a pre‑filled syringe or auto‑injector, following aseptic technique and rotating injection sites to reduce local irritation.

The most serious risks include severe liver injury, pulmonary fibrosis, life‑threatening bone‑marrow suppression leading to pancytopenia, acute renal failure, and rare but severe skin reactions such as Stevens‑Johnson syndrome. Prompt medical attention is required if any of these symptoms appear.

Metex is contraindicated in pregnant women, patients with severe hepatic or renal impairment, existing bone‑marrow failure, uncontrolled infections, and those receiving live vaccines. Caution is also advised for individuals with known hypersensitivity to methotrexate or any component of the formulation.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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