Product image of Namaxir (Methotrexate) supplied by GNH India

Namaxir

Active Ingredient:
Methotrexate
Origin:
EU

Namaxir (Methotrexate)

Methotrexate, the active ingredient in Namaxir, is an antimetabolite (folate antagonist) presented as an injection for epidural, intra‑articular, and intramuscular use. It is employed to treat rheumatoid arthritis, psoriatic arthritis, osteoarthritis pain, and other inflammatory joint conditions in adult patients under medical supervision and is approved for use in the European Union.

GNH India supplies Namaxir as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with a focus on reliable cold‑chain logistics and regulatory compliance, and timely delivery.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

Methotrexate is used in several inflammatory joint disorders, acting to reduce immune‑mediated damage.

  • Rheumatoid arthritis: reduces joint inflammation, pain, and slows structural damage.
  • Psoriatic arthritis: alleviates joint symptoms and prevents progression of joint erosion.
  • Osteoarthritis pain (inflammatory component): provides symptomatic relief of pain and swelling.
  • Other inflammatory joint conditions: manages pain and inflammation where standard therapies are insufficient.
  • Juvenile idiopathic arthritis: helps control disease activity and improve joint function in children.
  • Severe plaque psoriasis: decreases skin lesion severity when administered systemically.

How It Works

  • Methotrexate inhibits the enzyme dihydrofolate reductase, blocking the conversion of dihydrofolate to tetrahydrofolate. This interruption impairs synthesis of purine nucleotides and thymidylate, leading to reduced DNA replication and cell proliferation. In immune cells, the resulting antiproliferative effect diminishes the production of inflammatory cytokines, thereby exerting immunosuppressive and anti‑inflammatory actions.

Side Effects

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

Common Side Effects

  • Nausea and vomiting.
  • Fatigue or general weakness.
  • Mouth sores (stomatitis).
  • Elevated liver enzymes.
  • Decreased blood cell counts.
  • Headache.

Serious or Rare Side Effects

  • Severe liver toxicity or fibrosis.
  • Pulmonary fibrosis or interstitial pneumonitis.
  • Significant bone marrow suppression leading to pancytopenia.
  • Acute renal impairment.
  • Anaphylactic or severe hypersensitivity reactions.
  • Opportunistic infections due to immunosuppression.

Precautions & Warnings

When using methotrexate, careful monitoring and specific precautions are essential.

  • Monitor liver function: perform baseline and periodic liver enzyme tests.
  • Assess renal function: adjust dosing if renal impairment is present.
  • Evaluate blood counts: conduct regular complete blood count monitoring.
  • Avoid in pregnancy: drug is teratogenic and contraindicated (Category X).
  • Review concomitant medications: NSAIDs and other folate antagonists may increase toxicity.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Methotrexate interacts with several drug classes; awareness of major and moderate interactions helps prevent adverse events.

Major Interactions (Avoid)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): increase risk of renal toxicity.
  • Live vaccines: heightened risk of severe infection.
  • Other folate antagonists (e.g., aminopterin): additive toxicity.
  • High‑dose penicillins: may raise methotrexate plasma levels.
  • Trimethoprim‑sulfamethoxazole: enhances myelosuppression.

Moderate Interactions (Monitor Closely)

  • Proton pump inhibitors: may affect methotrexate absorption.
  • Sulfonamides: increase risk of hematologic toxicity.
  • Azathioprine: additive immunosuppressive effect.
  • Phenytoin: may alter methotrexate clearance.
  • Alcohol: can exacerbate liver toxicity.

Frequently Asked Questions

Namaxir contains methotrexate, which is prescribed for inflammatory joint disorders such as rheumatoid arthritis, psoriatic arthritis, osteoarthritis pain with an inflammatory component, and other severe inflammatory joint conditions where conventional therapy is insufficient.

Methotrexate blocks dihydrofolate reductase, disrupting folate metabolism and DNA synthesis. This limits the proliferation of immune cells and reduces the production of inflammatory cytokines, providing an immunosuppressive and anti‑inflammatory effect that helps control joint disease.

The specific dose of Namaxir is determined by the prescribing clinician based on the patient’s condition, weight, renal and hepatic function, and treatment response. Dosage regimens are individualized and should follow the prescriber’s instructions.

Methotrexate is classified as Pregnancy Category X because it is teratogenic and can cause fetal harm. It is contraindicated in pregnancy and should be stopped well before conception. Breastfeeding is not recommended while using methotrexate.

To place an order, 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 where required) and necessary import documentation.

Methotrexate is a folate antagonist and is often considered a first‑line disease‑modifying antirheumatic drug (DMARD). Compared with biologic agents, it is less expensive, administered via injection, and has a well‑characterized safety profile, though monitoring for hepatic and hematologic toxicity is essential.

Namaxir 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 product to maintain stability.

Namaxir is supplied as an injectable solution and can be given by a healthcare professional via epidural, intra‑articular, or intramuscular injection, depending on the therapeutic indication and clinical protocol.

Serious risks include severe liver toxicity, pulmonary fibrosis, bone‑marrow suppression leading to pancytopenia, renal impairment, and life‑threatening infections. Patients should be monitored regularly for liver enzymes, blood counts, and renal function.

Namaxir is contraindicated in pregnant or breastfeeding women, patients with severe liver or renal disease, those with known hypersensitivity to methotrexate, and individuals receiving live vaccines. Caution is also advised for patients with existing blood‑cell disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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